[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Igdir University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":160},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,48,83,111,135],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100651925","effects-of-met-and-mfr-on-piriformis-syndrome-100651925",false,"NCT07769203","Effects of MET and MFR on Piriformis Syndrome","The Effect of Muscle Energy Technique and Myofascial Release Technique on Pain Threshold, Muscle Activation Pattern, and Muscle Strength in Piriformis Syndrome","Inclusion Criteria:\n\n* Individuals diagnosed with piriformis syndrome\n* Presence of piriformis tenderness and sciatic symptoms\n* Aged between 18 and 65 years\n* Voluntary agreement to participate in the study\n* No history of lumbar, hip, knee, or ankle surgery within the last year\n* Ability to cooperate with the assessment and treatment procedures\n\nExclusion Criteria:\n\n* Individuals younger than 18 years or older than 65 years\n* Presence of any musculoskeletal disorder affecting the lower extremity\n* Presence of neurological, cardiac, pulmonary, or orthopedic disorders preventing participation in exercise\n* Presence of neurological deficits (muscle strength loss)\n* History of radiotherapy to the lumbar or hip region\n* Absence from more than 20% of treatment sessions\n* Inability to comply with the study procedures (e.g., cognitive impairment, communication problems, severe psychiatric disorders)\n* Corticosteroid or PRP injection within the last 3 months\n* Participation in another physical therapy program within the last 3 months\n* Use of analgesic, anti-inflammatory, or muscle relaxant medications within the last 48-72 hours\n* Use of psychotropic medications that may affect muscle activation or nervous system responses (e.g., antidepressants, antipsychotics, sedatives)","ALL","18 Years","65 Years",{"count":20,"type":21},72,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aim of this study is to comparatively evaluate the effects of two different manual therapy approaches, Muscle Energy Technique (MET) and Myofascial Release Technique (MFR), on pain threshold, muscle activation patterns, and muscle strength in individuals diagnosed with piriformis syndrome.\n\nIn this study, the physiological effects of both interventions on the musculoskeletal system will be assessed using objective measurement tools such as an algometer, digital dynamometer, and electromyography (EMG). The study aims to provide evidence-based data regarding the most effective and preferable manual therapy approach in the conservative treatment of piriformis syndrome.",[27],"Piriformis Syndrome",[27,29,30,31,32,33,34],"Muscle Energy Technique","Myofascial Release","Surface EMG","Pain Threshold","Muscle Strength","Rehabilitation","NOT_YET_RECRUITING","2026-08-12",{"date":38,"type":39},"2026-08-17","ACTUAL",{"date":41,"type":21},"2026-08-30",{"date":43,"type":21},"2026-12",{"name":45,"class":46},"Igdir University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":55,"sex":16,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":61,"conditions":62,"keywords":68,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":47},"100649221","two-different-therapeutic-interventions-applied-during-blood-sampling-in-children-100649221","NCT07731347","Two Different Therapeutic Interventions Applied During Blood Sampling in Children","The Effect of Two Different Therapeutic Interventions on Pain, Anxiety and Fear During Venipuncture in Children","Inclusion Criteria:\n\n* Being between 5 and 7 years old,\n* Having a scheduled venous blood sampling procedure in the Pediatric Emergency Unit,\n* Having a level of consciousness suitable for communication,\n* The child and their parents agreeing to participate in the study,\n* Being able to communicate in Turkish.\n\nExclusion Criteria:\n\nInability to participate in the application due to visual or hearing problems,\n\n* Inability to administer the scales due to a developmental or neurological disease,\n* Being under the influence of sedative or analgesic medication,\n* Inability to complete the application during the research process,\n* Lack of parental consent.",true,"5 Years","7 Years",{"count":59,"type":21},105,[24],"This research is a three-group, randomized controlled experimental study designed to determine the effect of two different therapeutic interventions applied during blood sampling on pain, anxiety, and fear levels in children aged 5-7 years.\n\nChildren participating in the study will be randomly divided into three groups:\n\n1. Group (Experiment 1): Distraction method using betta fish observation\n2. Group (Experiment 2): Distraction method using hand puppets\n3. Group (Control): Routine clinical practice (without any therapeutic intervention) Before, during, and after blood sampling, children's pain level (FLACC scale), fear level (child fear scale), and anxiety level (child anxiety scale) will be evaluated.",[63,64,65,66,67],"Blood Sampling","Child, Only","Pain","Fear","Nurse's Role",[69,70,71,72,73,74],"Play Therapy","blood sampling","child","pain","fear","nursing","2026-07-28",{"date":77,"type":39},"2026-07-29",{"date":79,"type":21},"2026-08-01",{"date":81,"type":21},"2026-12-01",{"name":45,"class":46},{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":89,"eligibilityCriteria":90,"healthyVolunteers":55,"sex":16,"minAge":91,"maxAge":92,"enrollmentInfo":93,"targetDuration":4,"studyType":22,"phases":95,"briefSummary":96,"conditions":97,"keywords":101,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":47},"100626719","turtle-assisted-animal-interaction-on-dental-anxiety-and-physiological-parameters-in-children-100626719","NCT07439289","Turtle-Assisted Animal Interaction on Dental Anxiety and Physiological Parameters in Children","Effects of Turtle-Assisted Animal Interaction on Dental Anxiety and Physiological Parameters in Children: A Randomized Controlled Trial","TAADA","Inclusion Criteria:\n\n* Children aged 6-10 years\n\n  * Children with ASA I-II general health status\n  * Children who have obtained written parental consent + an age-appropriate informed consent form\n  * Children undergoing non-invasive procedures that do not require local anesthesia, such as dental examinations, fissure sealant or fluoride application. • Children who can understand Turkish instructions (for scale application).\n\nExclusion Criteria:\n\n* • Children with animal phobia \u002F intense fear of turtles (as stated by the child or parent). • Children with immunosuppression or a history of severe allergic diseases. • Children with a dental plan requiring sedation\u002FGA within the last month (due to intense anxiety or systemic illness).\n\n  * Children with an active infectious disease \u002F a condition requiring isolation. • Children for whom a physician has deemed contact with animals inadvisable. • Children who have been included in a similar behavioral\u002Fanxiety intervention program during the same period.","6 Years","10 Years",{"count":94,"type":21},50,[24],"This study aims to measure the effect of a structured AAT session with a turtle present on dental anxiety and behavioral compliance in children during routine procedures that do not require local anesthesia in a pediatric dental clinic.",[98,99,100],"Animal-Human Bonding","Dental Anxiety","Pediatric Disease",[98,99,100],"RECRUITING","2026-07-23",{"date":105,"type":39},"2026-07-24",{"date":107,"type":39},"2026-03-01",{"date":109,"type":21},"2026-09-01",{"name":45,"class":46},{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":55,"sex":16,"minAge":57,"maxAge":118,"enrollmentInfo":119,"targetDuration":4,"studyType":22,"phases":120,"briefSummary":121,"conditions":122,"keywords":124,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":4},"100649006","effects-of-therapeutic-touch-and-music-on-childrens-anxiety-pain-and-nausea-before-and-after-circumcision-100649006","NCT07728266","Effects of Therapeutic Touch and Music on Children's Anxiety, Pain, and Nausea Before and After Circumcision","Effects of Therapeutic Touch and Music on Anxiety, Pain, and Nausea in Children Before and After Circumcision: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Children aged between 7 and 12 years\n* Children and parents who provide written and verbal informed consent\n* Children without any chronic diseases\n* Children and parents without visual impairments\n\nExclusion Criteria:\n\n* Children and parents who refuse to participate or do not volunteer for the study (do not sign the consent form)\n* Participants who display behaviors incompatible with the research content -Participants who subsequently refuse to participate in the research after initial consent\n* Participants with incomplete data","12 Years",{"count":59,"type":21},[24],"This randomized controlled trial aims to evaluate the effects of therapeutic touch and music therapy on anxiety, pain, and nausea in children undergoing circumcision surgery. Circumcision is a common surgical procedure, and children often experience significant anxiety, pain, and nausea both before and after the operation. The study involves children aged 7 to 12 years old who are scheduled for circumcision at Iğdır State Hospital. Participants will be randomly assigned to one of three groups: a therapeutic touch group, a music therapy group, or a control group. The goal of this research is to determine if applying non-pharmacological methods-specifically therapeutic touch or listening to music-for 15 minutes before and after the surgery can effectively reduce children's anxiety, pain levels, and nausea compared to standard care.",[123],"Circumcision",[123,125,126],"Therapeutic Touch","Music Therapy","2026-07-22",{"date":129,"type":39},"2026-07-27",{"date":131,"type":21},"2026-12-15",{"date":133,"type":21},"2027-03-12",{"name":45,"class":46},{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":4,"eligibilityCriteria":141,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":142,"targetDuration":4,"studyType":22,"phases":144,"briefSummary":145,"conditions":146,"keywords":148,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":4},"100638629","effect-of-warm-footbath-combined-with-relaxation-exercise-on-pain-and-anxiety-during-chest-tube-removal-after-cardiac-surgery-100638629","NCT07585240","Effect of Warm Footbath Combined With Relaxation Exercise on Pain and Anxiety During Chest Tube Removal After Cardiac Surgery","Effect of Warm Foot Bath Combined With Relaxation Exercise on Pain and Anxiety During Chest Tube Removal After Cardiac Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 18 years and older\n* Followed up with at least one chest tube after elective cardiac surgery -Scheduled for chest tube removal\n* Conscious, with a Glasgow Coma Scale (GCS) score of 15\n* Hemodynamically stable (Mean Arterial Pressure \\[MAP\\] ≥ 65 mmHg, and Peripheral Oxygen Saturation \\[SpO₂\\] ≥ 92% on room air or with routine oxygen support)\n* No visual or auditory impairments\n* Able to speAk and understand Turkish\n* No clinically diagnosed neurological or psychiatric disease, and not using regular psychotropic medications\n\nExclusion Criteria:\n\n* Aged under 18 years\n* Presence of diabetic peripheral neuropathy, peripheral vascular disease, or conditions disrupting foot\u002Fskin integrity (conditions where a warm water foot bath is contraindicated)\n* Hemodynamically unstable (Mean Arterial Pressure \\[MAP\\] \\\u003C 65 mmHg)\n* Presence of severe cognitive impairment, psychotic disorder, or hallucinations\n* Administered any analgesic medication outside the current analgesia protocol within the last 24 hours\n* Glasgow Coma Scale (GCS) score below 15\n* Inability to speak Turkish or presence of any condition preventing communication",{"count":143,"type":21},60,[24],"Chest tube removal is a widely used surgical procedure, particularly in the post-cardiac surgery period, to maintain cardiopulmonary stability, provide mediastinal drainage, and prevent potential complications. It provides one-way drainage of air and\u002For fluid accumulated in the pleural space through closed drainage systems. Chest tube removal is often described by patients as a painful and frightening experience. Without adequate pain control, chest tube removal can cause severe pain and anxiety in patients, limiting their physical activity and negatively impacting coughing and deep breathing. Consequently, this can lead to inadequate expansion of the thoracic cavity and predisposition to respiratory tract infections.\n\nPain management is considered a fundamental component of nursing care. Effective pain management relies on comprehensive assessment, application of appropriate pharmacological and non-pharmacological interventions, and monitoring of patient response. Pharmacological agents commonly used during chest tube removal include local anesthetics, opioid analgesics, and anti-inflammatory drugs. However, pharmacological methods can have side effects such as vomiting, nausea, respiratory distress, and hypotension, which can reduce patient comfort. Therefore, given the frequent use and potential side effects of pharmacological methods, there is an increasing need for non-pharmacological methods that are safe, easy to apply, and have no side effects in pain and anxiety management. The literature reports that non-pharmacological interventions are effective in reducing pain felt during chest tube removal. Studies in the literature show that relaxation exercises, a non-pharmacological method, are cost-effective, easy to apply, and effective in reducing pain and anxiety levels. These exercises have been shown to provide physiological relaxation by supporting muscle activation and are effective in pain management in patients after surgical procedures. Another non-pharmacological method used to reduce postoperative pain and anxiety is warm foot baths. Warm foot baths are reported to increase peripheral temperature, causing vasodilation, supporting autonomic balance, and providing physiological relaxation. While studies evaluating the effects of warm foot baths on pain and anxiety in various clinical situations exist in the literature, no study examining its effect during chest tube removal has been found. This indicates a significant knowledge gap in the literature regarding the potential effects of warm foot baths during chest tube removal. Accordingly, this research was planned to determine the effects of relaxation exercises applied before chest tube removal and warm foot baths applied simultaneously with relaxation exercises on pain and anxiety levels in patients undergoing cardiac surgery. The research will be conducted using a two-arm, parallel-group, randomized comparative experimental design. Considering the effect sizes reported in the literature for similar interventions and accounting for both literature-based and repeated-measures calculations, a median effect size was assumed. Accordingly, the study targeted a sample size of 30 patients per group (total n=60). The relaxation group (R) and the warm water footbath group (WWF+R) will be assigned using a block-randomized design. The R group will receive guided breathing and progressive muscle relaxation exercises. The WBB+R group will receive guided breathing and progressive muscle relaxation exercises, along with a warm-water foot bath. The interventions will begin with a pre-application to familiarize patients with the procedures. In the second phase, patients will perform the procedures 15 minutes before the scheduled chest tube removal time. Data will be collected at four time points using the Visual Analog Scale and the State Anxiety Scale. Appropriate statistical methods will be used for data analysis. This research has the potential to be the first randomized comparative study examining the simultaneous effects of a warm-water foot bath and relaxation exercises during chest tube removal after cardiac surgery. The findings are expected to contribute a new, low-cost, non-invasive, and evidence-based intervention to post-surgical nursing care protocols. The research outcomes are expected to improve patient comfort and the quality of clinical care.",[147],"Chest Tube Removal",[149,150,151,72],"chest tube removal","warm foot bath","anxiety","2026-05-09",{"date":154,"type":39},"2026-05-13",{"date":156,"type":21},"2026-05-01",{"date":158,"type":21},"2027-05",{"name":45,"class":46},""]