[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Tokat Gaziosmanpasa University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":506},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,18,0,[8,48,74,105,133,161,183,207,233,260,289,316,343,377,404,427,454,476],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":4},"100651635","neurodynamic-tensioning-plus-grip-strengthening-for-hand-grip-strength-100651635",false,"NCT07762937","Neurodynamic Tensioning Plus Grip Strengthening for Hand Grip Strength","Effect of Neurodynamic Tensioning Added to a Grip Strengthening Program on Hand Grip Strength: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged between 18 and 40 years.\n* Willing to participate voluntarily in the study.\n* No history of upper-extremity pain, injury, or surgery within the previous three months.\n* No diagnosed neurological, rheumatological, or systemic disease affecting the peripheral nervous system.\n* Sufficient cognitive ability to understand and follow the study protocol.\n\nExclusion Criteria:\n\n* History of carpal tunnel syndrome, cervical radiculopathy, peripheral neuropathy, or upper-extremity entrapment neuropathy.\n* History of upper-extremity fracture or surgery within the previous six months.\n* Regular participation in grip strengthening exercises or intensive upper-extremity resistance training.\n* Use of medication that may affect neuromuscular performance.",true,"ALL","18 Years","40 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"NA","This randomized controlled trial will investigate whether adding neurodynamic tensioning to a grip strengthening program provides additional improvements in hand grip strength in healthy adults. Sixty participants aged 18 to 40 years will be randomly assigned to two groups. Both groups will perform a standardized grip strengthening program for six weeks, three days per week. The experimental group will additionally receive neurodynamic tensioning exercises targeting the median and ulnar nerves. Hand grip strength will be assessed at baseline, week 3, and week 6. The study aims to determine whether neurodynamic tensioning provides additional benefit beyond grip strengthening alone.",[28,29,30],"Hand","Grip","Nerve",[32,33,34,35],"Neurodynamic Tensioning","Grip Strengthening","Resistance Training","Healthy Adults","NOT_YET_RECRUITING","2026-08-10",{"date":39,"type":40},"2026-08-13","ACTUAL",{"date":42,"type":22},"2026-09-15",{"date":44,"type":22},"2027-01-15",{"name":46,"class":47},"Tokat Gaziosmanpasa University","OTHER",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":67,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":73},"100651548","turkish-validation-of-the-core-life-activities-scale-100651548","NCT07762963","Turkish Validation of the Core Life Activities Scale","Turkish Version of the Core Life Activities Scale: Validity and Reliability Study","CORE-TR","Inclusion Criteria:\n\nAdults aged 18 years or older. Ability to read and understand Turkish fluently. No cognitive or physical impairment that would prevent completion of the questionnaires.\n\nWillingness to participate voluntarily and provide informed consent.\n\nExclusion Criteria:\n\nDiagnosis of a severe psychiatric or neurological disorder such as schizophrenia, bipolar disorder, or dementia.\n\nPresence of a terminal or severe medical condition that substantially affects activities of daily living, such as advanced-stage cancer or severe cardiovascular disease.\n\nLanguage barriers that prevent adequate understanding of the questionnaires. Providing inconsistent, intentionally inaccurate, or implausibly rapid questionnaire responses.",{"count":57,"type":22},300,"OBSERVATIONAL","This study aims to adapt the Core Life Activities Scale (CORE) into Turkish and evaluate its validity and reliability in Turkish-speaking adults. The CORE is a five-item self-report scale that assesses five basic areas of daily life: eating, sleeping, physical activity, learning new things, and social relationships. Approximately 300 adults aged 18 years and older will participate in the study. Participants will complete the Turkish version of the CORE together with measures of health-related quality of life. The CORE will also be administered again one week later to evaluate test-retest reliability. The findings will determine whether the Turkish version of the CORE is a valid and reliable tool for assessing core life activities in Turkish-speaking adults.",[61],"Life Style, Healthy",[63,64,65,66],"Validity","Reliability","Activities of Daily Living","Physical Activity",{"date":39,"type":40},{"date":69,"type":22},"2026-08-20",{"date":71,"type":22},"2026-09-30",{"name":46,"class":47},1,{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":17,"minAge":82,"maxAge":83,"enrollmentInfo":84,"targetDuration":4,"studyType":23,"phases":86,"briefSummary":87,"conditions":88,"keywords":91,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":73},"100648953","the-effect-of-sound-based-interventions-on-pain-and-anxiety-in-pediatric-patients-100648953","NCT07727109","The Effect of Sound-Based Interventions on Pain and Anxiety in Pediatric Patients","Effects of Non-Pharmacological Auditory Interventions on Pain and Anxiety in Pediatric Patients: A Randomized Controlled Trial Comparing White and Pink Noise","PED-SOUND-PAIN","Inclusion Criteria:\n\n* Children between 7-12 years of age.\n* Scheduled for a peripheral intravenous (IV) catheterization procedure.\n* No know hearing impairment.\n* Parents\u002Flegal guardians willing and able to provide written informed consent.\n\nExclusion Criteria:\n\n* History of chronic pain or neurological disorder.\n* Use of any analgesic or sedative medication within 24 hours prior to the procedure.\n* Requiring emergency intervention (emergency catheterization).\n* inability to communicate or understand the procedure.","6 Years","12 Years",{"count":85,"type":22},150,[25],"This study is a prospective, three-arm, single-blind, randomized controlled clinical trial designed to evaluate the effectiveness of non-pharmacological sound-based interventions on pain and anxiety in pediatric patients. The study will be conducted at a university hospital with 150 children aged 6-12 years who require peripheral intravenous (IV) catheterization. Participants will be randomly assigned to three groups: a white noise group, a pink noise group, or a control group (standard care). Sound interventions (white or pink noise at 50-55 dB) will be administered via noise-canceling headphones for 5 minutes before and during the IV procedure. The primary outcomes will be pain levels assessed by the Visual Analog Scale (VAS) and the Wong-Baker FACES Pain Rating Scale, and anxiety levels assessed by the Children's Fear and Anxiety Scale (CFAS). The study aims to provide evidence-based, safe, and cost-effective alternatives to pharmacological pain management in pediatric clinical procedures.",[89,90],"Pain (Visceral, Somatic, or Neuropathic)","Anxiety Acute",[92,93,94,95,96],"pediatric pain","anxiety","white noise","pink noise","non-pharmacologiacal ıntervention","2026-07-22",{"date":99,"type":40},"2026-07-27",{"date":101,"type":22},"2026-09-01",{"date":103,"type":22},"2027-01-01",{"name":46,"class":47},{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":16,"sex":112,"minAge":18,"maxAge":4,"enrollmentInfo":113,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":115,"conditions":116,"keywords":120,"overallStatus":125,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":130,"leadSponsor":132,"locationsCount":73},"100645618","mindfulness-based-postpartum-discharge-education-on-maternal-role-and-anxiety-100645618","NCT07702058","Mindfulness-Based Postpartum Discharge Education on Maternal Role and Anxiety","The Effects of Mindfulness-Based Postpartum Discharge Education on Mothers' Maternal Role Perception and Anxiety Levels","Inclusion Criteria:\n\n* Mothers aged 18 and older who voluntarily agree to participate in the study\n* Mothers who have had a healthy singleton birth\n* Mothers who are in the postpartum ward within the first 24 hours after delivery\n* Mothers living in the same home environment with their baby\n* Mothers who can read and understand Turkish and fully complete the questionnaires\n* Mothers who can use mobile communication tools (e.g., WhatsApp)\n* Mothers whose health status is suitable to participate in the education process\n\nExclusion Criteria:\n\n* Mothers with serious physical or psychiatric illnesses in the postpartum period\n* Mothers whose newborns are admitted to the intensive care unit or have serious health problems\n* Mothers who have previously participated in a mindfulness-based education or therapy program\n* Mothers who cannot participate regularly in the education process or maintain communication during the follow-up period\n* Mothers who incompletely fill out the questionnaires or do not participate in the post-test phase","FEMALE",{"count":114,"type":22},84,"This study will be conducted as a quasi-experimental research with a pretest-posttest control group design at the Obstetrics and Gynecology Clinic of Tokat Gaziosmanpaşa University Research and Practice Hospital, aiming to evaluate the effects of mindfulness-based postpartum discharge education on mothers' maternal role perception and anxiety levels. The sample will consist of 84 postpartum women (42 in the experimental group and 42 in the control group) who meet the inclusion criteria, determined through G\\*Power analysis. Stratified randomization will be used for group allocation. Data will be collected using a Personal Information Form, the Maternal Role Perception Scale, and the Postpartum Specific Anxiety Scale. Within the first 24 hours postpartum (baseline\u002Fpretest), the experimental group will receive a 60-minute individual \"Mindfulness-Based Postpartum Education Program\" administered by the researcher in addition to routine discharge care, while the control group will receive only standard hospital discharge education. One week after the education, a second measurement will be applied to both groups. Subsequently, the experimental group will be systematically followed up for one month via WhatsApp with weekly reminder messages and monitoring charts. At the end of the first postpartum month (30th day), the final posttest measurements will be completed. The effects of the education over repeated time points will be analyzed using SPSS 22.0 software with descriptive statistics, parametric tests (Independent\u002FPaired Sample t-test, repeated measures Two-Way ANOVA, Pearson correlation), and non-parametric tests (Mann Whitney U, Wilcoxon, Spearman correlation) at a significance level of 0.05.",[117,118,119],"Postpartum Period","Anxiety","Maternal Behavior",[121,122,123,124],"Mindfulness","Maternal Role","Discharge Education","Midwifery","RECRUITING","2026-07-09",{"date":128,"type":40},"2026-07-14",{"date":126,"type":40},{"date":131,"type":22},"2026-12-31",{"name":46,"class":47},{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":139,"eligibilityCriteria":140,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":141,"targetDuration":4,"studyType":23,"phases":143,"briefSummary":144,"conditions":145,"keywords":148,"overallStatus":125,"whyStopped":4,"lastUpdateSubmitDate":153,"lastUpdatePostDateStruct":154,"startDateStruct":156,"completionDateStruct":158,"leadSponsor":160,"locationsCount":73},"100644412","the-effect-of-motivational-interventions-led-pregnancy-on-stress-and-alexithymia-in-couples-100644412","NCT07663812","THE EFFECT OF MOTIVATIONAL INTERVENTIONS LED PREGNANCY ON STRESS AND ALEXITHYMIA IN COUPLES","THE EFFECT OF MOTIVATIONAL INTERVENTIONS LED BY MIDWIVES DURING PREGNANCY ON STRESS AND ALEXITHYMIA IN COUPLES","ALEXITHYMIA","Inclusion Criteria:\n\n* For pregnant women:\n\n  * Agreement to participate in the study\n  * Being 18 years of age or older and married\n  * Being in the second trimester\n  * No pregnancy-related risks (such as preeclampsia, diabetes, heart disease, placenta previa, or oligohydramnios),\n  * No issues related to fetal health (such as fetal anomalies or intrauterine growth restriction),\n  * Ability to speak Turkish,\n  * No history of chronic or psychiatric conditions,\n\nFor partners:\n\n* Agreeing to participate in the study,\n* Accompanying their partner during the second trimester of pregnancy,\n* Not having a diagnosed psychiatric condition (depression, anxiety disorder, bipolar disorder, etc.),\n* Being able to speak and understand Turkish,\n\nExclusion Criteria:\n\n* • Participants deciding to withdraw from the study at any stage,\n\n  * Inability to contact the pregnant woman and\u002For her partner before the data collection process is completed,\n  * The pregnant woman being diagnosed with a high-risk pregnancy during the data collection process.",{"count":142,"type":22},140,[25],"The aim of this study is to examine the effect of midwife-led motivational interviewing during pregnancy on couples' stress and alexithymia levels.",[146,147],"Stress Levels During Pregnancy","Levels of Alexithymia During Pregnancy",[149,150,151,152],"Levels of Alexithymia,","Levels of Stress,","Motivational Interviewing","Pregnant","2026-06-23",{"date":155,"type":40},"2026-06-26",{"date":157,"type":40},"2026-01-28",{"date":159,"type":22},"2026-10-30",{"name":46,"class":47},{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":165,"acronym":4,"eligibilityCriteria":166,"healthyVolunteers":16,"sex":112,"minAge":18,"maxAge":4,"enrollmentInfo":167,"targetDuration":4,"studyType":23,"phases":169,"briefSummary":170,"conditions":171,"keywords":173,"overallStatus":125,"whyStopped":4,"lastUpdateSubmitDate":175,"lastUpdatePostDateStruct":176,"startDateStruct":178,"completionDateStruct":180,"leadSponsor":182,"locationsCount":73},"100640659","the-relationship-between-oxytocin-massage-in-mothers-with-insufficient-milk-production-in-the-early-postpartum-period-and-breastfeeding-self-efficacy-and-milk-let-down-reflex-a-randomized-controlled-study-100640659","NCT07609693","The Relationship Between Oxytocin Massage in Mothers With Insufficient Milk Production in the Early Postpartum Period and Breastfeeding Self-Efficacy and Milk Let-down Reflex: A Randomized Controlled Study","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Being in the early postpartum period (within the first 24-48 hours after birth)\n* Having had a single, live birth via vaginal delivery or cesarean section\n* Having a term (≥37 weeks) and healthy baby\n* Being in the same room as the baby (rooming-in practice)\n* Having started breastfeeding\n* Reporting insufficient milk production or expressing difficulty with the milk let-down reflex\n* Not having a cognitive, neurological, or serious psychiatric problem that would impede communication\n* Voluntary participation in the study and providing written informed consent\n\nExclusion Criteria:\n\n* Having given birth preterm (\\\u003C37 weeks)\n* Having given birth as a result of a multiple pregnancy\n* Having been admitted to the neonatal intensive care unit (NICU)\n* The baby having a congenital anomaly that prevents breastfeeding (e.g., cleft lip and palate)\n* The mother having medical conditions that contraindicate breastfeeding (HIV infection, active tuberculosis, etc.)\n* The mother developing serious postpartum complications (postpartum hemorrhage, eclampsia, serious infection, etc.)\n* The presence of anatomical or pathological conditions related to the breast that may prevent breastfeeding (advanced mastitis, breast abscess, etc.)\n* The presence of skin lesions, surgical incisions, or infections in the back that would prevent the application of oxytocin massage\n* Failure to complete the intervention or wishing to withdraw from the study will be excluded.",{"count":168,"type":22},128,[25],"This randomized controlled trial aims to evaluate the effects of oxytocin massage on breastfeeding self-efficacy and the milk ejection reflex among mothers experiencing insufficient milk supply in the early postpartum period. Insufficient milk supply is a common issue often linked to maternal stress, which can inhibit oxytocin release and negatively impact the milk ejection reflex and the mother's confidence in breastfeeding. By applying oxytocin massage to the thoracic paravertebral region, this study seeks to stimulate oxytocin release non-pharmacologically. The primary objective is to determine whether this intervention improves physiological milk flow and enhances maternal breastfeeding self-efficacy compared to routine postpartum care.",[172],"Lactation Disorders",[172,174,117],"Breast Feeding","2026-05-20",{"date":177,"type":40},"2026-05-27",{"date":179,"type":40},"2026-05-12",{"date":181,"type":22},"2026-09-12",{"name":46,"class":47},{"id":184,"slug":185,"hasResults":11,"nctId":186,"briefTitle":187,"officialTitle":187,"acronym":4,"eligibilityCriteria":188,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":189,"enrollmentInfo":190,"targetDuration":4,"studyType":23,"phases":192,"briefSummary":193,"conditions":194,"keywords":197,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":200,"lastUpdatePostDateStruct":201,"startDateStruct":203,"completionDateStruct":205,"leadSponsor":206,"locationsCount":4},"100631538","the-effect-of-color-rotation-technique-training-on-nslin-self-management-n-diabetic-patients-100631538","NCT07501988","The Effect Of Color Rotation Technique Training On İnsülin Self-management İn Diabetic Patients.","Inclusion Criteria :\n\n* Between the ages of 18-65\n* At least a primary school graduate\n* Diagnosed with Type 1 or Type 2 Diabetes for at least six months\n* Receiving insulin treatment\n* Capable of self-administering insulin injections\n* Free from psychiatric illness or communication impairment (vision, hearing, and speech)\n* Able to use a mobile phone and send and receive SMS messages\n* Administering insulin injections 4 times a day\n* Individuals who agree to participate in the study\n\nExclusion Criteria:\n\n* Not using insulin treatment-Using an insulin pump\n* Having temporary insulin treatment\n* Having lipodystrophy-Individuals who refused to participate in the study or who discontinued their education","65 Years",{"count":191,"type":22},112,[25],"Diabetes mellitus (DM) is a chronic disease characterized by impaired carbohydrate, protein, and lipid metabolism, resulting from a deficiency of insulin hormone secreted by the pancreas and\u002For the body's inability to utilize it even when sufficient insulin is secreted. As a frequently observed chronic disease, diabetes is a significant public health problem; if left uncontrolled, it can lead to serious complications and negatively impact quality of life.Individual management of treatment is crucial for successful treatment and glycemic control in diabetes. Due to the complexity of diabetes management related to insulin use, diabetics require greater self-care skills. Nurses play a crucial role in developing desired self-management behaviors in individuals with diabetes, supporting them, and meeting their needs.",[195,196],"Diabete Mellitus","İnsulin Self-management",[195,198,199],"İnsulin self-management","Nurse","2026-04-07",{"date":202,"type":40},"2026-04-08",{"date":204,"type":22},"2026-04-15",{"date":97,"type":22},{"name":46,"class":47},{"id":208,"slug":209,"hasResults":11,"nctId":210,"briefTitle":211,"officialTitle":212,"acronym":4,"eligibilityCriteria":213,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":214,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":216,"conditions":217,"keywords":220,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":225,"lastUpdatePostDateStruct":226,"startDateStruct":228,"completionDateStruct":230,"leadSponsor":232,"locationsCount":73},"100619976","turkish-version-of-the-pain-metacognitions-questionnaire-100619976","NCT07351617","Turkish Version of the Pain Metacognitions Questionnaire","Translation, Validity, and Reliability of the Turkish Version of the Pain Metacognitions Questionnaire","Inclusion Criteria:\n\n* Aged 18 years and older\n* Experiencing chronic non-cancer pain for at least three months\n* Ability to read and understand Turkish\n* Voluntary participation and provision of informed consent\n\nExclusion Criteria:\n\n* Presence of cancer-related pain\n* Severe cognitive impairment preventing completion of questionnaires\n* Incomplete or incorrectly completed questionnaires",{"count":215,"type":22},210,"Pain-related thoughts and beliefs play an important role in how individuals experience and cope with chronic pain. Metacognitions about pain, such as beliefs about the uncontrollability or harmfulness of pain-related thoughts, may influence emotional distress and pain-related outcomes. The Pain Metacognitions Questionnaire was developed to assess these beliefs; however, a validated Turkish version is not currently available. The aim of this study is to translate the Pain Metacognitions Questionnaire into Turkish and to evaluate its validity and reliability in adults with chronic non-cancer pain. This observational study will include adult individuals experiencing chronic pain for at least three months. Data will be collected using self-report questionnaires administered in a single assessment session. The findings of this study are expected to provide a reliable and valid measurement tool for assessing pain-related metacognitions in Turkish-speaking populations and to support future clinical and research applications in chronic pain management.",[218,219],"Chronic Pain","Pain Metacognitions",[221,222,223,224],"chronic pain","pain metacognitions","questionnaire validation","reliability","2026-01-10",{"date":227,"type":40},"2026-01-20",{"date":229,"type":22},"2026-02-01",{"date":231,"type":22},"2026-06-10",{"name":46,"class":47},{"id":234,"slug":235,"hasResults":11,"nctId":236,"briefTitle":237,"officialTitle":238,"acronym":4,"eligibilityCriteria":239,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":240,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":242,"conditions":243,"keywords":247,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":253,"lastUpdatePostDateStruct":254,"startDateStruct":256,"completionDateStruct":258,"leadSponsor":259,"locationsCount":73},"100619149","physical-fatigue-compassion-fatigue-and-quiet-quitting-in-physiotherapists-100619149","NCT07340866","Physical Fatigue, Compassion Fatigue, and Quiet Quitting in Physiotherapists","Physical Fatigue, Compassion Fatigue, and Quiet Quitting Tendency Among Physiotherapists in Türkiye: A Cross-Sectional Study","Inclusion Criteria:\n\n* Graduated from a Physiotherapy and Rehabilitation undergraduate program\n* Actively working as a physiotherapist in Türkiye\n* Voluntary participation and provision of informed consent\n\nExclusion Criteria:\n\n* Refusal to participate in the study\n* Working in a profession other than physiotherapy\n* Incomplete or incorrectly completed questionnaires",{"count":241,"type":22},80,"Physiotherapists are exposed to both physical and emotional demands due to the nature of their profession. Repetitive physical workload, prolonged standing, patient handling, and continuous interaction with patients may contribute to physical fatigue and compassion fatigue. These factors may negatively affect work engagement and lead to a phenomenon known as quiet quitting, which refers to reduced psychological involvement in work without formally leaving the job.\n\nThe aim of this study is to examine levels of physical fatigue and compassion fatigue among physiotherapists working in Türkiye and to investigate their association with quiet quitting tendencies. This observational, cross-sectional study will include physiotherapists actively working in public or private healthcare settings. Data will be collected using validated self-report questionnaires administered online and face-to-face.\n\nUnderstanding the relationship between occupational fatigue and quiet quitting may help inform strategies to improve well-being, job satisfaction, and sustainability in the physiotherapy workforce.",[244,245,246],"Quiet Quitting","Fatigue, Compassion","Work Engagement",[248,249,250,251,252],"fatigue","compassion fatigue","work engagement","occupational health","quiet quitting","2026-01-05",{"date":255,"type":40},"2026-01-14",{"date":257,"type":22},"2026-02-22",{"date":179,"type":22},{"name":46,"class":47},{"id":261,"slug":262,"hasResults":11,"nctId":263,"briefTitle":264,"officialTitle":265,"acronym":4,"eligibilityCriteria":266,"healthyVolunteers":16,"sex":112,"minAge":267,"maxAge":268,"enrollmentInfo":269,"targetDuration":4,"studyType":23,"phases":270,"briefSummary":271,"conditions":272,"keywords":275,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":281,"lastUpdatePostDateStruct":282,"startDateStruct":284,"completionDateStruct":286,"leadSponsor":288,"locationsCount":73},"100610869","the-effect-of-wireless-electronic-fetal-monitoring-on-labor-pain-and-birth-experiences-100610869","NCT07233187","The Effect of Wireless Electronic Fetal Monitoring on Labor Pain and Birth Experiences","The Effect of Continuous Wireless Fetal Monitoring During the Intrapartum Period on Labor Pain and Birth Experience: A Randomized Controlled Single-Blind Study","Inclusion Criteria:\n\n* The study included healthy primiparous or multiparous pregnant women who agreed to participate in the study, were between the ages of 18 and 35, had a gestational age greater than 37+0, had cervical dilation greater than 4 cm, had a single, live fetus, were not using uterotonic agents, spoke Turkish, had no comprehension, perception, or communication problems, and were healthy.\n\nExclusion Criteria:\n\n* Pregnant women who were diagnosed with a risky pregnancy, who were illiterate, who had a contagious disease, or who had a risky disease were not included in the study.","19 Years","35 Years",{"count":191,"type":22},[25],"This study is using Electronic Fetal Monitoring (EFM) to assess fetal health in pregnant women in labor. This will be compared with continuous wired EFM and continuous wireless EFM. The effects of wireless and continuous wireless EFM on labor pain levels and labor experiences will be measured.",[273,274],"Birth","Intrapartum",[276,277,278,279,280],"Fetal Monitoring","intrapartum","pain","birth experience","Continuous Wireless Fetal Monitoring","2025-11-14",{"date":283,"type":40},"2025-11-18",{"date":285,"type":22},"2025-11-15",{"date":287,"type":22},"2026-01-15",{"name":46,"class":47},{"id":290,"slug":291,"hasResults":11,"nctId":292,"briefTitle":293,"officialTitle":293,"acronym":294,"eligibilityCriteria":295,"healthyVolunteers":16,"sex":112,"minAge":18,"maxAge":296,"enrollmentInfo":297,"targetDuration":4,"studyType":23,"phases":298,"briefSummary":299,"conditions":300,"keywords":302,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":309,"lastUpdatePostDateStruct":310,"startDateStruct":312,"completionDateStruct":313,"leadSponsor":315,"locationsCount":73},"100608252","the-effect-of-haptonomy-practice-on-body-functionality-appreciation-and-childbirth-self-efficacy-in-pregnant-women-100608252","NCT07199140","The Effect of Haptonomy Practice on Body Functionality Appreciation and Childbirth Self-Efficacy in Pregnant Women","HAP-Func-Eff","Inclusion Criteria:\n\n* Aged 18 years or older\n* Spontaneous pregnancy at 28 weeks of gestation\n* Primiparous (first pregnancy)\n* Able to read and write in Turkish\n* Healthy singleton pregnancy\n\nExclusion Criteria:\n\n* Any health problems in the mother or fetus\n* History of complications during pregnancy\n* Diagnosed psychiatric disorders or use of psychiatric medication\n* Any physical, mental, or cognitive disabilities","50 Years",{"count":241,"type":22},[25],"Study Type and Aim:\n\nThis clinical study aims to examine the effects of haptonomy practices on appreciation of bodily functionality and childbirth self-efficacy among healthy pregnant women. The study seeks to determine whether haptonomy can enhance these two outcomes.\n\nKey Research Questions:\n\nDo haptonomy practices increase appreciation of bodily functionality in pregnant women? Do haptonomy practices increase childbirth self-efficacy in pregnant women?\n\nComparison:\n\nResearchers will compare an intervention group receiving haptonomy sessions with a control group receiving only routine prenatal care to evaluate the effects of the intervention.\n\nParticipants will:\n\nParticipants will provide written informed consent to take part in the study. Pregnant women in the intervention group will attend four haptonomy sessions, each lasting approximately 45 minutes and held at 7-day intervals. Sessions will include practices to enhance body awareness, relaxation techniques, connecting with the baby, and affirmations supporting bodily functionality and childbirth self-efficacy.\n\nPregnant women in the control group will receive routine prenatal care and follow-up only.\n\nAll participants will complete pretest and posttest measures assessing appreciation of bodily functionality and childbirth self-efficacy.\n\nKeywords: Haptonomy, Vaginal birth, Pregnancy, Prenatal care, Body functionality appreciation, Birth self-efficacy",[301],"Pregnant Women",[303,304,305,306,307,308],"Haptonomy","Pregnancy","Body functionality appreciation","Vaginal birth","Prenatal care","Birth self-efficacy","2025-09-22",{"date":311,"type":40},"2025-09-30",{"date":285,"type":22},{"date":314,"type":22},"2026-06-15",{"name":46,"class":47},{"id":317,"slug":318,"hasResults":11,"nctId":319,"briefTitle":320,"officialTitle":321,"acronym":4,"eligibilityCriteria":322,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":323,"targetDuration":4,"studyType":23,"phases":325,"briefSummary":326,"conditions":327,"keywords":329,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":335,"lastUpdatePostDateStruct":336,"startDateStruct":338,"completionDateStruct":340,"leadSponsor":342,"locationsCount":4},"100604808","internet-based-emdr-flash-intervention-for-test-anxiety-in-university-students-100604808","NCT07154329","Internet-Based EMDR Flash Intervention for Test Anxiety in University Students","Examining the Effect of Internet-Based EMDR Flash Intervention (SKY-Flash) on University Students' Test Anxiety Levels and User Experiences","Inclusion Criteria:\n\nVoluntary participation in the study Being older than 18 years and currently enrolled as a university student Having a valid e-mail address Having internet access (computer or mobile device) Scoring above the average on the Test Anxiety Scale Scoring below 15 on the Patient Health Questionnaire-9 (PHQ-9), based on established cutoff points\n\nExclusion Criteria:\n\nCurrently receiving psychological help from a psychologist, counselor, or psychiatrist Having any diagnosed psychiatric disorder",{"count":324,"type":22},168,[25],"The aim of this study is to investigate whether an Internet-based EMDR Flash intervention can help reduce exam anxiety among university students. Participants will utilize the online SKY-Flash program and report their levels of exam anxiety at pre-intervention, post-intervention, and follow-up assessments. In addition, the study will collect feedback regarding participants' overall experiences with the program. The primary objective is to determine whether SKY-Flash constitutes a practical and effective approach to reducing exam anxiety among students, while also exploring their perceptions of the intervention.",[328],"Test Anxiety",[330,331,332,333,334],"Internet-based intervention","EMDR Flash","Psychological Well-Being","University Students","Randomized Controlled Trial","2025-09-03",{"date":337,"type":40},"2025-09-10",{"date":339,"type":22},"2026-03-15",{"date":341,"type":22},"2026-06-30",{"name":46,"class":47},{"id":344,"slug":345,"hasResults":11,"nctId":346,"briefTitle":347,"officialTitle":348,"acronym":349,"eligibilityCriteria":350,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":351,"enrollmentInfo":352,"targetDuration":4,"studyType":23,"phases":354,"briefSummary":355,"conditions":356,"keywords":362,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":369,"lastUpdatePostDateStruct":370,"startDateStruct":372,"completionDateStruct":374,"leadSponsor":376,"locationsCount":73},"100603596","kinesio-taping-for-the-knee-and-ankle-acute-impact-on-balance-proprioception-and-acl-risk-100603596","NCT07138573","Kinesio Taping for the Knee and Ankle: Acute Impact on Balance, Proprioception, and ACL Risk","Evaluation and Comparison of the Acute Effects of Kinesio Taping Applied to the Knee and Ankle in the Lower Extremity on Balance, Proprioception, and Anterior Cruciate Ligament Injury Risk Using the Landing Error Scoring System (LESS)","ACL","Inclusion Criteria:\n\n* Volunteering to participate in the study\n* Being 18 years of age or older\n* Being a licensed and regular volleyball player for at least 5 years\n\nExclusion Criteria:\n\n* Being enrolled in another study or treatment program\n* Being unable to complete the study for any other reason\n* Having suffered a lower extremity injury within 6 months prior to participating in the study\n* Female participants must be in their menstrual cycle","45 Years",{"count":353,"type":22},24,[25],"This study aims to evaluate and compare the acute effects of Kinesio taping applied to the knee and ankle on balance, proprioception, and anterior cruciate ligament (ACL) injury risk using the Landing Error Scoring System (LESS). Designed as a randomized crossover trial, the study will include 24 healthy volleyball athletes with at least 5 years of experience. All participants will receive both ankle and knee taping interventions, separated by a one-week washout period. Assessments will be conducted at four time points: before and after each taping. Outcome measures include the Y-Balance Test, proprioception tests, and LESS.",[357,358,359,360,361],"ACL Injury","Kinesiotape","Balance","Proprioception","Landing Error Scoring System (LESS)",[363,364,365,366,367,361,368],"ankle","knee","acl injury","balance","proprioception","kinesiotape","2025-08-21",{"date":371,"type":40},"2025-08-24",{"date":373,"type":22},"2025-08-30",{"date":375,"type":22},"2025-12-30",{"name":46,"class":47},{"id":378,"slug":379,"hasResults":11,"nctId":380,"briefTitle":381,"officialTitle":382,"acronym":4,"eligibilityCriteria":383,"healthyVolunteers":16,"sex":17,"minAge":384,"maxAge":82,"enrollmentInfo":385,"targetDuration":4,"studyType":23,"phases":386,"briefSummary":387,"conditions":388,"keywords":390,"overallStatus":125,"whyStopped":4,"lastUpdateSubmitDate":396,"lastUpdatePostDateStruct":397,"startDateStruct":399,"completionDateStruct":401,"leadSponsor":403,"locationsCount":73},"100593247","the-effect-of-different-deproteinizing-agents-on-the-clinical-success-of-fissure-sealants-in-primary-teeth-100593247","NCT07003958","The Effect of Different Deproteinizing Agents on the Clinical Success of Fissure Sealants in Primary Teeth","Evaluation of the Effect of Different Deproteinizing Agents on the Clinical Success of Fissure Sealants in Primary Teeth: Splint Mouth Clinical Study","Inclusion Criteria:\n\n* Patients between the ages of 4-6 who do not have any systemic problems\n* Have a score of 3 and 4 on the Frankl Behavior Scale\n* Do not have a habit of clenching and\u002For grinding their teeth\n* Have lower second primary molars without caries\n* Have an indication for fissure sealant application\n\nExclusion Criteria:\n\n* Teeth with fissure sealants\n* Teeth with developmental defects such as hypoplasia\n* Teeth with approximal or incipient caries lesions on one or both mandibular second primary molars","4 Years",{"count":21,"type":22},[25],"Investigation of the effect of deproteinization agents on the clinical success of non-invasive fissure sealant application, which is a non-invasive method used to prevent caries formation or to stop the progression of initial caries lesions limited to enamel on tooth surfaces thought to be at high risk of caries.",[389],"Fissure Sealant",[391,392,393,394,395],"deproteinization agents","sodium hypochlorite","hypochlorous acid","fissure sealent","Primary Teeth","2025-05-26",{"date":398,"type":40},"2025-06-04",{"date":400,"type":40},"2024-08-05",{"date":402,"type":22},"2026-08-05",{"name":46,"class":47},{"id":405,"slug":406,"hasResults":11,"nctId":407,"briefTitle":408,"officialTitle":409,"acronym":4,"eligibilityCriteria":410,"healthyVolunteers":16,"sex":17,"minAge":82,"maxAge":411,"enrollmentInfo":412,"targetDuration":4,"studyType":23,"phases":413,"briefSummary":387,"conditions":414,"keywords":415,"overallStatus":125,"whyStopped":4,"lastUpdateSubmitDate":419,"lastUpdatePostDateStruct":420,"startDateStruct":422,"completionDateStruct":424,"leadSponsor":426,"locationsCount":73},"100592028","the-effect-of-different-deproteinising-agents-on-the-clinical-success-of-fissure-sealants-in-permanent-teeth-100592028","NCT06988098","The Effect of Different Deproteinising Agents on the Clinical Success of Fissure Sealants in Permanent Teeth","Evaluation of the Effect of Different Deproteinizing Agents on the Clinical Success of Fissure Sealants in Permanent Teeth: Splint Mouth Clinical Study","Inclusion Criteria:\n\n* Patients between the ages of 6-9 who do not have any systemic problems\n* Have a score of 3 and 4 on the Frankl Behavior Scale\n* Do not have a habit of clenching and\u002For grinding their teeth\n* Have newly erupted permanent lower first molars without caries\n* Have an indication for fissure sealant application\n\nExclusion Criteria:\n\n* Teeth with fissure sealants\n* Teeth with developmental defects such as hypoplasia\n* Teeth with approximal or incipient caries lesions on one or both mandibular first permanent molars\n* Children who are not systemically healthy\n* Uncooperative children with scores of 1 and 2 on the Frankl Behavior Scale\n* Children and parents who refuse to attend follow-up appointments\n* Children with parafunctional habits such as teeth grinding","9 Years",{"count":21,"type":22},[25],[389],[416,417,418,394],"Deproteinization Agents","Sodium Hypochlorite","Hypochlorous Acid","2025-05-16",{"date":421,"type":40},"2025-05-23",{"date":423,"type":40},"2024-08-01",{"date":425,"type":22},"2027-08-01",{"name":46,"class":47},{"id":428,"slug":429,"hasResults":11,"nctId":430,"briefTitle":431,"officialTitle":432,"acronym":4,"eligibilityCriteria":433,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":434,"targetDuration":4,"studyType":23,"phases":436,"briefSummary":437,"conditions":438,"keywords":440,"overallStatus":125,"whyStopped":4,"lastUpdateSubmitDate":446,"lastUpdatePostDateStruct":447,"startDateStruct":449,"completionDateStruct":451,"leadSponsor":453,"locationsCount":73},"100575446","teaching-electronic-fetal-monitoring-to-midwifery-students-with-peer-teaching-method-100575446","NCT06772389","Teaching Electronic Fetal Monitoring to Midwifery Students With Peer Teaching Method","The Effect of Electronic Fetal Monitoring Training Given to Midwifery Students With Peer Education Method on the Knowledge, Skills and Self-Efficacy Levels of the Students","Inclusion Criteria:\n\n* volunteers to participate in the study,\n* those taking the Prenatal Period-I course for the first time,\n* those who have not received any EFM training before,\n* those who are second year Midwifery students\n\nExclusion Criteria:\n\n* Students who are absent on the day the EFM topic is taught.",{"count":435,"type":22},72,[25],"706 \u002F 5.000 The aim of the study is to examine the effects of Electronic Fetal Monitoring (EFM) (a test that evaluates fetal health during pregnancy) training given to midwifery students through peer education method on the knowledge, skills and self-efficacy levels of the students. It is being conducted as an experimental study with a randomized controlled pre-test-post-test design. Students were given standard training on EFM. Students in the peer teaching group were given peer education. Students continue to be evaluated while applying EFM to pregnant women in clinical practice. Personal information form, achievement test for EFM, skill form and Electronic Fetal Monitoring Self-Efficacy Scale were used in the evaluation of the students.",[439],"Educational Problems",[441,442,443,444,445],"midwifery","education","cardiotocography","Clinical Skill","peer group","2025-01-13",{"date":448,"type":40},"2025-01-14",{"date":450,"type":40},"2024-12-03",{"date":452,"type":22},"2025-02-02",{"name":46,"class":47},{"id":455,"slug":456,"hasResults":11,"nctId":457,"briefTitle":458,"officialTitle":458,"acronym":4,"eligibilityCriteria":459,"healthyVolunteers":11,"sex":17,"minAge":19,"maxAge":189,"enrollmentInfo":460,"targetDuration":4,"studyType":23,"phases":462,"briefSummary":463,"conditions":464,"keywords":466,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":468,"lastUpdatePostDateStruct":469,"startDateStruct":471,"completionDateStruct":473,"leadSponsor":475,"locationsCount":4},"100572177","effect-of-yoga-eye-exercises-and-musculoskeletal-physiotherapy-interventions-on-presbyopia-100572177","NCT06729879","Effect of Yoga Eye Exercises and Musculoskeletal Physiotherapy Interventions on Presbyopia","Inclusion criteria Being between the ages of 40-65, Being diagnosed with presbyopia by an ophthalmologist, Having the mental capacity to understand and perform the exercises, Not having a systemic disease that prevents exercise, Agreeing to participate in the study\n\nExclusion Criteria; People with a history of eye surgery, People with refractive errors such as myopia, hyperopia, astigmatism, etc., People with a history of head-neck and upper extremity surgery, Being diagnosed with strabismus, Being diagnosed with glaucoma, Having a neurological problem affecting visual functions, Being diagnosed with cataract, Having a history of eye inflammation",{"count":461,"type":22},52,[25],"In this study, the effects of neck exercises, neck massage and yoga eye exercises on presbyopia will be examined. 52 patients diagnosed with presbyopia will be included in the study. The study is single-center and will be conducted in the Tokat Gaziosmanpaşa University Hospital, Department of Ophthalmology outpatient clinic.The study will be grouped into 4 groups. The person who agrees to participate in the study will be assigned to a group. In these groups, the first group will be subjected to eye exercises. The second group will be subjected to neck exercises and massages. The third group will be subjected to eye exercises, neck exercises and massages. The fourth group will not be subjected to any intervention. The participants in the study will be evaluated before the intervention and 8 weeks later. The doctor will conduct evaluations with an eye-related device and the physiotherapist will evaluate the questionnaire, reading speed and neck angles using the photographing method.",[465],"Presbiyopi",[467],"Presbyopia, Yoga eye exercises, Myofascial release, Postural exercise","2024-12-07",{"date":470,"type":40},"2024-12-11",{"date":472,"type":22},"2025-01-15",{"date":474,"type":22},"2025-09-15",{"name":46,"class":47},{"id":477,"slug":478,"hasResults":11,"nctId":479,"briefTitle":480,"officialTitle":480,"acronym":4,"eligibilityCriteria":481,"healthyVolunteers":11,"sex":17,"minAge":82,"maxAge":83,"enrollmentInfo":482,"targetDuration":4,"studyType":23,"phases":484,"briefSummary":485,"conditions":486,"keywords":494,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":498,"lastUpdatePostDateStruct":499,"startDateStruct":501,"completionDateStruct":503,"leadSponsor":505,"locationsCount":73},"100566498","the-effect-of-gardening-activities-on-anxiety-and-psychosocial-symptoms-of-hospitalized-children-100566498","NCT06655961","The Effect of Gardening Activities on Anxiety and Psychosocial Symptoms of Hospitalized Children","Inclusion Criteria:\n\n* The age of the children is between 6-12 years old\n* Hospitalization due to an acute medical diagnosis\n* Hospitalization for at least 3 days\n* Approval of the child's participation in the session by the responsible doctor\n* The child is conscious and fully orientated\n* Voluntariness of the child and parent to participate in the study\n\nExclusion Criteria:\n\n* Hospitalization for more than 7 days\n* No previous hospitalization experience\n* High-risk drug use\n* Having a chronic disease that suppresses the immune system\n* Having a special condition that prevents him\u002Fher from participating in garden activities (physical, mental disability)\n* Having skin conditions that prevent them from participating in garden activities\n* Plant allergy",{"count":483,"type":22},36,[25],"The experience of hospitalization in childhood can often lead to traumatic consequences. Various practices (play, art therapy, music therapy, etc.) are used to help children cope with this process. In recent years, attention has been drawn to nature-based approaches in addition to existing practices. Within the scope of this approach, this study was planned in a parallel group (experimental-control) randomized controlled experimental design to determine the effect of garden activities on anxiety levels and psychosocial symptoms of hospitalized children aged 6-12 years. Hypotheses of the study H1: The gardening activities program applied to hospitalized children; H1a: There is an effect on children's anxiety. H1b: There is an effect on psychosocial symptoms of children. In this direction, the population of the study will consist of children between the ages of 6-12 in the children's ward of University Research and Application Hospital. The sample size determined as a result of G\\*power analysis was found as control (18) and intervention (18). The research will be conducted between September 2024 and June 2025. 'Child Descriptive Information Form', \"Child Follow-up Form\", \"Child Anxiety Scale-Conditioning\" and \"Psychosocial Symptoms Diagnostic Scale for Hospitalized Children\" will be used for data collection. The data collection process consists of three stages: pre-intervention period, intervention period and post-intervention period. Children in the intervention group will have three sessions of gardening activities within the scope of the 'Gardening Activities Program' during their hospitalization. Children in the control group will receive services within the scope of the routine treatment and nursing care protocol of the clinic during hospitalization.",[487,488,489,490,118,491,492,493],"Gardening","Pediatric Nursing","Activity","Psychosocial Symptoms","Hospital","Child","Investigation of Anxiety Levels and Psychosocial Symptoms of Children Hospitalized for Acute Diseases During Their Hospital Stay",[495,496,488,490,118,497],"Hospitalized Child","Garden Activity","Mobile Garden","2024-10-22",{"date":500,"type":40},"2024-10-24",{"date":502,"type":22},"2024-12",{"date":504,"type":22},"2025-09",{"name":46,"class":47},""]