Clinical trials

105

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Video-Based Self-Assessment in Neonatal Resuscitation Training

The aim of this study is to evaluate the effects of video-based self-assessment in simulation-based neonatal resuscitation skills training on neonatal resuscitation skills, clinical judgment, student satisfaction, and self-confidence.

Participants needed: 84
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Oct 13, 2026Locations: 1
Eligibility criteria

Volunteering to participate in the study. [+3]

Having previously attended a Neonatal Resuscitation Program, certificate trainin... [+3]

Status: Not yet recruiting

Digital Flashcards for Fluid and Electrolyte Education in Surgical Nursing: A Solomon Four-Group Study

This study aims to investigate the effect of the digital flashcard method, compared to traditional lecturing, on students' knowledge levels and self-efficacy perceptions regarding fluid-electrolyte balance in the surgical nursing course, within a Solomon four-group experimental design framework.

Participants needed: 180
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Oct 9, 2026Locations: 1
Eligibility criteria

Being enrolled in the Surgical Nursing Course [+2]

Having previously taken the Surgical Nursing Course [+1]

Status: Not yet recruiting

Relationship Between Interoception and Postural Control in Constipation-Predominant Irritable Bowel Syndrome

This cross-sectional, observational, controlled comparative study aims to investigate the relationship between interoception and postural control in individuals with constipation-predominant irritable bowel syndrome (IBS-C) and to compare the findings with those of healthy individuals. Interoception will be assessed using the Multidimensional Assessment of Interoceptive Awareness-2 (MAIA-2), postural characteristics will be evaluated using the Corbin Posture Analysis, and stool type in the IBS-C group will be assessed using the Bristol Stool Scale.

Participants needed: 128
Trial details
Age: 18-45Biological sex: AllType: ObservationalSponsor: Saglik Bilimleri UniversitesiUpdated: Oct 13, 2026Locations: 1
Eligibility criteria

Aged 18-45 years. [+3]

Having a neurological, rheumatological, or serious orthopedic disease. [+3]

Status: Recruiting

Markers of Bone Destruction and Oxidative Stress in Peri-implantitis

The aim of this study is to evaluate and compare the levels of bone resorption (RANKL, OPG) and oxidative stress (Nitrotyrosine, NQO1) markers, along with pro-inflammatory cytokines (IL-1β), in the saliva and peri-implant sulcular fluid (PISF) of patients with peri-implantitis, periodontitis, and healthy individuals. The study seeks to determine the diagnostic value of these biomarkers in the early detection and progression of peri-implant diseases.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Qigong Intervention for Fibromyalgia

This randomized controlled pilot study investigates the comparative efficacy of mobility-intensive Qigong exercises versus static posture-based Qigong exercises in patients diagnosed with fibromyalgia. Participants are randomly allocated to either a mobility-intensive Qigong intervention group or a static posture-based Qigong intervention group. The primary objectives are to evaluate improvements in spinal mobility and reductions in pain levels. Secondary outcomes include enhancements in functional exercise capacity, reductions in fatigue severity, and improvements in health-related quality of life. All outcome assessments are conducted at baseline and upon completion of the intervention program.

Participants needed: 36
Trial details
Age: 30-50Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 24, 2026Locations: 1
Eligibility criteria

Female patients aged between 30 and 50 years. [+4]

Pregnancy or currently breastfeeding. [+5]

Status: Recruiting

Clinical Evaluation of Customized Attachment Composites in Clear Aligner Therapy

This prospective observational clinical study aims to evaluate the three-dimensional surface wear and clinical survival of orthodontic attachments fabricated with customized composite materials used in clear aligner therapy. Attachments play a critical role in the biomechanical efficiency of aligner treatment by facilitating planned tooth movements. However, the mechanical and surface properties of the composites used for attachment fabrication may affect their wear behavior and long-term stability. In this study, four different composite materials will be tested using a split-mouth design in patients treated with clear aligners. Each quadrant will receive a different composite, including both customized and universal types. All attachments will be fabricated using standardized digital templates and bonded under identical clinical conditions. Surface wear will be evaluated using three-dimensional optical scanning and metrology software at baseline, 1 week, 1 month, 3 months, and 6 months. Lost attachments will be replaced and recorded but excluded from wear analysis. The results of this study are expected to provide valuable insights into the optimal material selection for clear aligner attachments, improving treatment accuracy and clinical durability.

Participants needed: 24
Trial details
Biological sex: AllType: ObservationalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 22, 2026Locations: 1
Eligibility criteria

Fully erupted permanent dentition. [+4]

History of previous fixed orthodontic treatment. [+9]

Status: Not yet recruiting

Effects of Irrigation Solutions at Different Temperatures Used in Mandibular Third Molar Surgery

The present study aims to compare the effects of saline, chlorhexidine, and hydrogen peroxide irrigation solutions at different temperatures on postoperative complications, including pain, swelling, and mouth opening, as well as oral health-related quality of life, in patients undergoing surgical extraction of impacted mandibular third molars. The irrigation solutions will be applied immediately following surgical tooth extraction at temperatures of either 4°C or 25°C. An a prior power analysis based on repeated-measures analysis of variance (Repeated Measures ANOVA, within-between interaction) was performed. An effect size of f = 0.25, a Type I error rate (α = 0.05), and a statistical power of 1 - β = 0.95 were assumed. Based on the power analysis, a minimum of 11 participants per group was determined to be sufficient. Considering potential loss to follow-up and missing data, the sample size was increased by approximately 15%, and it was decided to enroll 13 participants in each group. Accordingly, the planned study will be conducted with a total of 78 participants allocated to six groups, and all participants will be evaluated at four different time points.

Participants needed: 78
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

Presence of a unilateral or bilateral impacted mandibular third molar classified... [+3]

Individuals outside the specified age range. [+12]

Status: Not yet recruiting

Circadian Rhythm and Cardiovascular Recovery After Submaximal Exercise

This cross-sectional, observational, and analytical study aims to investigate the relationship between morningness-eveningness characteristics and cardiovascular recovery after a submaximal exercise test in healthy individuals aged 18-45 years. Circadian preference will be assessed using the Morningness-Eveningness Questionnaire, sleep quality will be assessed using the Pittsburgh Sleep Quality Index, and cardiovascular recovery will be evaluated following the 6-Minute Walk Test

Participants needed: 124
Trial details
Age: 18-45Biological sex: AllType: ObservationalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 22, 2026Locations: 1
Eligibility criteria

Aged 18-45 years. [+2]

Presence of cardiovascular, pulmonary, neurological, or orthopedic disease. [+3]

Status: Recruiting

Dental Loupe Versus Dental Operating Microscope for Non-Surgical Periodontal Treatment

Periodontitis is a multifactorial, non-infectious disease that can lead to tooth loss if left untreated. Advanced stages of periodontitis can affect chewing ability, nutritional status, and quality of life. Calculus removal, root planing, and mechanical removal of plaque should be considered a fundamental part of initial periodontal treatment. Furthermore, patients who undergo calculus removal and root planing followed by regular maintenance programs experience less tooth loss and clinical attachment loss. Calculus removal and root planing are integral parts of non-surgical periodontal treatment to remove bacterial plaque and calculus from diseased root surfaces. The use of magnification systems to increase the field of view in both surgical and non-surgical procedures dates back to the 1860s with the first use of surgical microscopes. Magnification systems were first used in dentistry in the first half of the 20th century. In 1978, Apotheker and Jako developed the first surgical microscope for use in dentistry. The use of magnifying loupes as visual aids by dentists has become increasingly popular over the years, with continuous improvements in design and effectiveness. A 2019 survey among dentists indicated that magnifying lenses are one of the significant technological advancements in this profession. Periodontal endoscopy is also one of the approaches clinicians use to improve visibility. Dental magnification systems are known to increase effectiveness, especially in interproximal areas where access and visibility are limited. Clinical studies have compared root surface planing procedures performed with periodontal endoscopy with traditional root surface planing. The results of the studies showed a significant difference in clinical outcomes in patients treated with periodontal endoscopy compared to those treated with traditional methods. The aim of this study is to analyze the clinical and microbiological benefits of image magnification systems (dental loupe and dental microscope) in scaling and root surface planing in the treatment of patients with periodontitis.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 21, 2026Locations: 3
Eligibility criteria

Being over 18 years of age [+7]

Patients under 18 years of age [+6]

Status: Recruiting

Interoception and Symptom Perception in Acute COPD Exacerbation

Interoception refers to the process of perceiving and interpreting internal physiological signals and plays a central role in symptom perception. In conditions with a high symptom burden such as chronic obstructive pulmonary disease (COPD), clinical features including dyspnea perception, depression, and sleep quality may be influenced not only by disease severity but also by the interpretation of internal bodily signals. Recent evidence suggests that respiratory-related internal signals are transmitted to the central nervous system through multiple afferent pathways and integrated within cortical and subcortical networks, contributing to subjective experiences such as dyspnea. In this context, dyspnea perception may arise from the interaction between disease severity and interoceptive processes. Depressive symptoms and impaired sleep quality are also closely associated with interoceptive processes and may contribute to the perception of respiratory symptoms. However, studies simultaneously examining interoception, disease severity, dyspnea perception, depression, and sleep quality in hospitalized patients with acute COPD exacerbation are limited. This prospective, observational, cross-sectional study will include 50 individuals aged 40 years and older who are hospitalized with acute COPD exacerbation in a Chest Diseases clinic. Data will be collected at a single time point when patients are clinically stable, without interfering with routine clinical care. Participants will be recruited using a consecutive sampling method. Sociodemographic and clinical data will be obtained from patient records and a structured data collection form. Disease severity will be assessed using oxygen requirement, respiratory rate, oxygen saturation, and arterial blood gas values when available. Interoception will be evaluated using the Multidimensional Assessment of Interoceptive Awareness (MAIA-2). Symptom burden will be assessed with the COPD Assessment Test (CAT), dyspnea with the Modified Medical Research Council (mMRC) scale, sleep quality with the Richards-Campbell Sleep Questionnaire (RCSQ), and depressive symptoms with the Hospital Anxiety and Depression Scale - Depression subscale (HADS-D). Statistical analyses will be performed using IBM SPSS Statistics software. Relationships between variables will be analyzed using Pearson or Spearman correlation depending on data distribution, with a significance level of p\<0.05.

Participants needed: 50
Trial details
Age: 40-75Biological sex: AllType: ObservationalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 17, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Physician-confirmed diagnosis of acute exacerbation of COPD with hospitalization [+3]

Presence of delirium or severe cognitive impairment [+6]

Status: Recruiting

Treatment of Intrabony Defects With Injectable Platelet-Rich Fibrin and Xenogenic Grafts

The use of injectable platelet-rich fibrin (i-PRF) in both surgical and non-surgical dental treatments has become increasingly widespread. Hard tissue grafts can produce "sticky bone," and bone gain can have a positive effect on intrabony defects frequently seen in periodontal disease, compared to grafts alone. This study aims to clinically and radiographically evaluate the effectiveness of using bovine-derived xenogenic bone grafts in combination with i-PRF and bovine-derived xenogeneic bone grafts alone in patients with intrabony defects and stage III periodontitis.

Participants needed: 16
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 11, 2026Locations: 1
Eligibility criteria

Male and female patients aged 18-65 years [+4]

Patients under 18 years of age or older than 65 years of age [+11]

Status: Not yet recruiting

Titanium Particle Release Across Non-Surgical Peri-implantitis Therapies

This prospective, randomized, controlled, single-blind, in vivo clinical and laboratory study aims to quantitatively compare the clinical success and metal ion release associated with four different non-surgical decontamination methods in the management of peri-implantitis. A total of 70 implants (56 peri-implantitis implants divided into four treatment groups, and 14 healthy control implants) will be included. Clinical parameters will be evaluated at baseline and 6 weeks, and multi-element trace metal levels (Ti, Al, V, Co, Cr, Cu, Zr, Fe, Ni, As, Pb) in peri-implant sulcular fluid (PISF) and granulation tissue will be analyzed using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) at baseline, 24 hours, and 6 weeks.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 10, 2026
Eligibility criteria

Being systemically healthy and older than 18 years of age. [+2]

Having received systemic antibiotic therapy within the past 3 months. [+2]

Status: Not yet recruiting

Evaluation of the Effects of Injectable Platelet-Rich Fibrin and Hyaluronic Acid Treatments, Administered in Addition to Free Gingival Graft Therapy, on Clinical Healing.

The purpose of this clinical trial is to evaluate the effects of injectable platelet-rich fibrin (i-PRF) and hyaluronic acid (HA) gel on clinical healing and graft shrinkage when used in addition to Free Gingival Graft (FGG) surgery. The study involves patients with gingival recession and insufficient keratinized tissue. Participants will be randomly divided into three groups: FGG with i-PRF application, FGG with HA gel application, Conventional FGG alone (Control group). The main goal is to compare the amount of graft shrinkage and evaluate clinical wound healing parameters between these groups over a 3-month follow-up period.

Participants needed: 45
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 4, 2026Locations: 1
Eligibility criteria

Individuals aged 18 years or older. [+4]

Patients with systemic diseases that may affect wound healing (e.g., uncontrolle... [+4]

Status: Recruiting

High-Intensity Interval Exercise in Bronchiectasis Patients

The aim of our study is to investigate the effect of high-intensity interval exercise (HIIE) on the symptoms of bronchiectasis in patients with the disease. The main questions it aims to answer are: 1. Does HIIE improve respiratory function in patients with bronchiectasis? 2. Does HIIE increase functional capacity, peripheral muscle strength, and quality of life in patients with bronchiectasis? 3. Does HIIE reduce the severity of dyspnea, cough symptoms, and fatigue in patients with bronchiectasis? The study was designed as a randomized controlled trial. Participants were divided into two groups: intervention and control. Participants will: The intervention group will receive HIIE training three days a week along with airway clearance techniques. The control group would receive only airway clearance techniques. Airway clearance techniques will be provided clinically (three days a week) and at home, according to the needs of the individuals each day of the week.

Participants needed: 42
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 4, 2026Locations: 1
Eligibility criteria

Being over 18 years of age [+3]

Presence of any disease that may affect compliance with exercise (Unstable angin... [+5]

Status: Recruiting

Mediterranean and Low-Histamine Diets for Pediatric Chronic Spontaneous Urticaria

Chronic spontaneous urticaria (CSU) is a chronic inflammatory skin disease that can substantially impair quality of life in children and adolescents. Pharmacological treatment may not adequately control symptoms in all patients, increasing interest in dietary interventions. This randomized controlled trial aims to compare the effects of a Mediterranean diet and a low-histamine diet, in addition to standard medical treatment, on disease activity, disease control, and quality of life in pediatric patients aged 12-18 years with chronic spontaneous urticaria. Participants will be allocated to one of three groups: standard treatment alone, standard treatment plus a low-histamine diet, or standard treatment plus a Mediterranean diet. The dietary intervention will last four weeks, with follow-up through eight weeks.

Participants needed: 63
Trial details
Age: 12-18Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Sep 4, 2026Locations: 1
Eligibility criteria

Age 12-18 years. [+3]

Presence of a neurodevelopmental disorder. [+5]

Status: Recruiting

The Effect of Ostomy Care Education Applied With the Teach-Back Method to Ostomy-Opened Individuals on Self-Care Power, Ostomy Adjustment, and Anxiety

The aim of this study is to examine the effect of ostomy care education-delivered to patients who have undergone ostomy surgery using the Teach-back method on patients' self-care ability, ostomy compliance, and anxiety levels.

Participants needed: 44
Trial details
Age: 18-84Biological sex: AllType: ObservationalSponsor: Saglik Bilimleri UniversitesiUpdated: Aug 26, 2026Locations: 1
Eligibility criteria

Having an ostomy [+6]

Having a poor general health condition [+3]

Status: Not yet recruiting

Effects of Connective Tissue Massage in Patients With Chronic Insomnia

This randomized controlled trial will investigate the effects of connective tissue massage on insomnia severity, objective and subjective sleep outcomes, and stress- and autonomic-related biomarkers in adults with chronic insomnia. Chronic insomnia is a common sleep disorder characterized by persistent difficulties in initiating or maintaining sleep and is associated with impaired daytime functioning, reduced cognitive performance, and diminished quality of life. Non-pharmacological interventions may provide a safe alternative or complementary approach for individuals with chronic insomnia. A total of 74 adults diagnosed with chronic insomnia by a neurologist and who have not used sleep medication during the previous four weeks will be enrolled. Participants will be randomly allocated to either a connective tissue massage group or a control group. The intervention group will receive 12 sessions of connective tissue massage over a four-week period, with three sessions per week, in addition to sleep hygiene education. The control group will receive sleep hygiene education alone. Assessments will be performed at baseline and immediately after the four-week intervention period. The primary outcome will be the change in insomnia severity, assessed using the Insomnia Severity Index. Secondary outcomes will include objective sleep parameters recorded by actigraphy over five consecutive days, including total sleep time, sleep efficiency, sleep onset latency, and wake after sleep onset. Blood biomarkers associated with hypothalamic-pituitary-adrenal axis activity and autonomic regulation, including cortisol, DHEA-S, alpha-amylase, and oxytocin, will also be assessed. Subjective sleep quality and sleep hygiene will be evaluated using the Pittsburgh Sleep Quality Index and Sleep Hygiene Index, respectively. Adherence to sleep hygiene recommendations will additionally be assessed using sleep diaries. The study aims to determine whether connective tissue massage combined with sleep hygiene education is more effective than sleep hygiene education alone in reducing insomnia severity and improving objective and subjective sleep outcomes and selected physiological biomarkers in adults with chronic insomnia.

Participants needed: 74
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Aug 18, 2026Locations: 1
Eligibility criteria

Adults aged 18 to 65 years, of either sex. [+6]

History of shift work during the previous month or lifestyle changes that may di... [+5]

Status: Not yet recruiting

Maternal Periodontal Inflammation and Pregnancy Outcomes: Salivary and Amniotic Biomarkers

Periodontal disease is a chronic inflammatory condition that affects the tissues supporting the teeth and may contribute to systemic inflammation and oxidative stress. Increasing evidence suggests that maternal inflammation during pregnancy may be associated with adverse pregnancy outcomes, including preterm birth. However, the biological mechanisms linking maternal periodontal inflammation to the intrauterine environment remain unclear. This prospective observational cohort study aims to investigate the relationship between maternal periodontal status and inflammatory and oxidative stress biomarkers measured in both saliva and amniotic fluid. Eighty healthy pregnant women between 28 and 32 weeks of gestation will be recruited from the Obstetrics and Gynecology Clinic of Gulhane Training and Research Hospital. Participants will undergo a comprehensive periodontal examination and provide unstimulated saliva samples. Amniotic fluid samples will be collected during delivery as part of routine obstetric care, without any additional invasive procedures. The concentrations of 8-hydroxy-2'-deoxyguanosine (8-OHdG), malondialdehyde (MDA), interleukin-6 (IL-6), and matrix metalloproteinase-8 (MMP-8) will be measured in saliva and amniotic fluid using enzyme-linked immunosorbent assay (ELISA). Pregnancy outcomes, including gestational age at delivery, birth weight, and pregnancy complications, will also be recorded. The study will evaluate whether maternal periodontal inflammation is associated with changes in inflammatory and oxidative stress biomarkers in saliva and amniotic fluid and whether these biomarkers are related to pregnancy outcomes. The findings may improve understanding of the biological relationship between oral health and pregnancy and may contribute to the identification of biomarkers associated with adverse pregnancy outcomes.

Participants needed: 80
Trial details
Age: 18-40Biological sex: FemaleType: ObservationalSponsor: Saglik Bilimleri UniversitesiUpdated: Jul 29, 2026
Eligibility criteria

Pregnant women between 28 and 32 weeks of gestation [+9]

Multiple pregnancy [+7]

Status: Recruiting

The Effects of Tele-Rehabilitation-Based Dual-Task Upper Extremity Training in Patients With Parkinson's Disease

The aim of this study is to compare the effects of tele-rehabilitation-based synchronous and asynchronous dual-task upper extremity training with clinical based dual-task upper extremity training and conventional single-task upper extremity training in patients with Parkinson's disease. The main questions it aims to answer are: * Whether there are differences in motor symptoms, hand dexterity, upper extremity functions, grip strength, executive functions, daily living activities, and treatment satisfaction between tele-rehabilitation-based synchronous and asynchronous dual-task upper extremity training, clinical-based dual-task upper extremity training, and conventional single-task upper extremity training in patients with Parkinson's disease. * Whether there is a difference in telemedicine satisfaction between tele-rehabilitation-based synchronous and asynchronous dual-task upper extremity training in patients with Parkinson's disease. Researchers will compare conventional single-task upper extremity training, clinical-based dual-task upper extremity training, tele-rehabilitation-based synchronous upper extremity training and tele-rehabilitation-based asynchronous upper extremity training. Participants will: * Receive upper extremity exercise training at the study clinic or home, twice a week for approximately 60 minutes each time, for 6 weeks. * Participate in assessments at the study clinic before and after exercise training.

Participants needed: 40
Trial details
Age: 40+Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Jul 7, 2026Locations: 1
Eligibility criteria

Having been diagnosed with Parkinson's disease by a neurologist according to the... [+3]

Presence of a neurological disease other than Parkinson's disease [+4]

Status: Not yet recruiting

Game-Based Psychological First Aid Training for Midwifery Students

Purpose: This study aims to evaluate the effects of an educational digital escape room game-based Psychological First Aid (PFA) training on the PFA self-efficacy and problem-solving levels of undergraduate midwifery students. Methods: The study will be conducted as a randomized controlled trial with a pretest, posttest, and follow-up design at the Health Sciences University (SBU), Hamidiye Faculty of Health Sciences, Department of Midwifery during the spring semester of the 2025-2026 academic year. Second-year midwifery students will be randomly assigned to either the intervention group or the control group using a stratified randomization method based on their Grade Point Average (GPA). Both groups will receive a standardized theoretical PFA training program. In addition to this training, the intervention group will participate in an interactive digital escape room game developed on the Genially platform, consisting of short web-based scenarios under 20 minutes. The control group will receive only the standard theoretical education. Data will be collected at baseline (Week 1), post-intervention (Week 3), and during follow-up phases using the Psychological First Aid Self-Efficacy Scale and the Problem Solving Inventory to compare the behavioral and educational outcomes between the two groups.

Participants needed: 84
Trial details
Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Jun 25, 2026
Eligibility criteria

Volunteering to participate in the research. [+4]

Being a passive student in the 2nd year of the Midwifery Department at Hamidiye... [+1]

Status: Not yet recruiting

THE EFFECT OF SIMULATION-BASED INTERPROFESSIONAL EDUCATION ON ATTITUDES TOWARD TEAMWORK

Our study aims to evaluate the effect of interprofessional simulation-based learning on teamwork attitudes among nursing and paramedic students during the patient handover process. The study sample consists of fourth-year (senior) students from the Gülhane Faculty of Nursing at the University of Health Sciences and second-year (senior) students from the Paramedic Program at the School of Health Professions. In this study, the intervention will be conducted in two phases: the preparation phase and the implementation phase.

Participants needed: 56
Trial details
Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Jun 23, 2026
Eligibility criteria

Be a 4th-year (senior) student in a bachelor's degree program in nursing [+6]

Must be a graduate of a vocational high school for health professions, [+2]

Status: Recruiting

Comparison of Two Different Dual-Task Training Methods in Patients With Parkinson's Disease

The aim of this study is to compare the effectiveness of motor-motor dual-task training and cognitive-motor dual-task training in patients with Parkinson's disease.The main questions it aims to answer are: \- Whether there is a difference between motor-motor dual-task training and cognitive-motor dual-task training in patients with Parkinson's disease in terms of their effects on motor symptoms, balance, gait, functional mobility, activities of daily living, dual-task activities, cognitive functions, and balance confidence. Researchers will compare single-task training, motor-motor dual task training and cogvitive-motor dual task training. Participants will: * Receive exercise training at the study clinic twice a week for approximately 45 minutes each time, for 6 weeks. * Participate in assessments at the study clinic before and after exercise training.

Participants needed: 39
Trial details
Age: 40+Biological sex: AllType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Having been diagnosed with Parkinson's disease by a neurologist according to the... [+1]

Presence of a neurological disease other than Parkinson's disease [+4]

Status: Not yet recruiting

The Effect of Breastfeeding Education Using the Pecha Kucha Technique on Breastfeeding Self-Efficacy and Breastfeeding Success in the Early Postpartum Period: A Randomized Controlled Trial

Breast milk is considered the most biologically appropriate source of nutrition, essential for the healthy growth and development of newborns. Thanks to its optimal nutrients, immunological factors, and growth regulators, it not only meets nutritional needs but also protects against infections, reducing neonatal morbidity and mortality rates. The Pecha Kucha presentation technique keeps presentations concise and dynamic, creating a fast-paced, light, and engaging experience. It minimizes distractions and maximizes engagement. Because there is no text to read in the Pecha Kucha technique, presenters are required to be more prepared and strive to create a coherent narrative, resulting in a flawless narrative. Thus, the aim is to ensure the success and effectiveness of breastfeeding education with this technique, and ultimately, to promote breastfeeding education using the Pecha Kucha technique to healthcare professionals. The population of this randomized, controlled experimental study consists of primiparous postpartum women who gave birth in the Obstetrics Department of the Physical Therapy Annex Building of the Gaziosmanpaşa Training and Research Hospital at the University of Health Sciences. A power analysis was conducted using the G\*Power package program, Version 3.1.9.4, to determine the sample size of the study. Because no similar research was found in the literature, Cohen's medium effect size was chosen as the effect size, anticipating that tests assessing the difference between two independent groups would be used when examining the differences in variables between the control and intervention groups. Accordingly, with 64 participants in the control group and 64 in the intervention group, a power of 80% was calculated at a significance level of 0.5 (medium) effect size and 0.05, and a minimum sample size of 128 was determined. The study, planned using an experimental design, is planned to be conducted on two groups: an intervention and a control group. Within the scope of the study, pretest data will be collected by administering the Breastfeeding Self-Efficacy Scale and the LATCH Breastfeeding Diagnostic and Assessment Scale, along with an introductory information form, to postpartum women who agree to participate in the study.

Participants needed: 128
Trial details
Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

- Being primiparous [+3]

Being multiparous (having given birth more than once) [+4]

Status: Not yet recruiting

Trauma-Informed Yoga Intervention in Young Women

The aim of this study is to evaluate the effects of a trauma-informed yoga intervention on psychological trauma symptoms, difficulties in emotion regulation, and interoceptive awareness in young adult women.

Participants needed: 46
Trial details
Age: 18-25Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: May 15, 2026Locations: 1
Eligibility criteria

Being a woman aged 18-25 years [+4]

Inability to provide reliable responses due to the presence of active psychotic... [+4]

Status: Recruiting

Prenatal Yoga Intervention in Pregnant Women

The aim of this study is to determine the effects of a prenatal yoga intervention on traumatic childbirth perception, self-perception, and delivery preferences in pregnant women.

Participants needed: 46
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: May 14, 2026Locations: 1
Eligibility criteria

Being at or beyond the 16th week of gestation (second trimester or later) [+4]

Diagnosis of high-risk pregnancy (e.g., preeclampsia, placenta previa, premature... [+4]