Clinical trials

39

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

Condition / disease
Location
Status: Not yet recruiting

Sleep Quality in Adolescents With Idiopathic Scoliosis

This controlled cross-sectional observational study aims to compare sleep quality between adolescents with idiopathic scoliosis and age- and sex-similar healthy controls. Participants aged 10-18 years will complete online questionnaires assessing demographic characteristics and sleep quality. Adolescents with idiopathic scoliosis will also be evaluated for scoliosis-specific quality of life, body image, Cobb angle, curve type, pain, brace use, and daily brace-wearing duration. The study will additionally investigate factors associated with sleep quality in the scoliosis group. The planned enrollment is 100 participants, including 50 adolescents with idiopathic scoliosis and 50 healthy controls.

Participants needed: 100
Trial details
Age: 10-19Biological sex: AllType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Aug 17, 2026
Eligibility criteria

Aged 10-19 years [+3]

Having a type of scoliosis other than adolescent idiopathic scoliosis [+7]

Status: Recruiting

Effectiveness of a Horse Riding Simulator in Adolescents With Idiopathic Scoliosis

Adolescent idiopathic scoliosis (AIS) is a three-dimensional spinal deformity associated with impaired respiratory muscle strength, balance, postural control, body image, and health-related quality of life. Core stabilization exercises are widely used in the conservative management of AIS. Horse riding simulator training reproduces the multidirectional rhythmic movements of horseback riding while eliminating the potential risks associated with conventional hippotherapy and may provide additional benefits for postural control and trunk muscle activation. The aim of this randomized controlled trial is to investigate the effects of adding horse riding simulator training to a core stabilization exercise program on respiratory muscle strength, balance, health-related quality of life, and perceived cosmetic deformity in adolescents with idiopathic scoliosis. Participants will be randomly assigned to either an experimental group receiving horse riding simulator training combined with core stabilization exercises or a control group receiving core stabilization exercises alone. Outcomes will be assessed before and after the 12-week intervention.

Participants needed: 30
Trial details
Age: 10-19Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Aug 11, 2026Locations: 1
Eligibility criteria

Diagnosis of adolescent idiopathic scoliosis [+3]

Scoliosis of a non-idiopathic etiology [+4]

Status: Recruiting

Effect of Proximal Segment Positioning on Condylar Remodeling

This study aims to evaluate postoperative condylar remodeling in patients undergoing bimaxillary orthognathic surgery by comparing two different proximal segment positioning techniques used during mandibular osteotomy. Condylar remodeling will be assessed using preoperative, immediate postoperative, and 6-month postoperative computed tomography (CT) scans together with clinical findings.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Aug 11, 2026Locations: 1
Eligibility criteria

Patients with skeletal Class III dentofacial deformity scheduled to undergo bima... [+3]

History of temporomandibular joint surgery, orthognathic surgery, or tumor resec... [+3]

Status: Recruiting

Structured Inpatient Physiotherapy in High-Risk Coronary Artery Bypass Grafting Patients

Coronary artery bypass grafting (CABG) may be associated with prolonged recovery, particularly in high-risk patients. Although preoperative rehabilitation has shown promising results, evidence remains limited because of heterogeneous intervention protocols and variations in postoperative care. This study aims to investigate the effects of a structured inpatient physiotherapy program initiated at least two days before surgery and continued postoperatively, compared with the same structured physiotherapy program provided only during the postoperative period, in high-risk CABG patients. The primary outcome is hospital length of stay. Secondary outcomes include intensive care unit length of stay, C-reactive protein, neutrophil-to-lymphocyte ratio, hemoglobin, dyspnea, and fatigue.

Participants needed: 100
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Jul 24, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older. [+1]

Planned redo CABG surgery. [+5]

Status: Recruiting

VR vs Treadmill Exercise in Children With Asthma

This study aims to compare the effects of virtual reality-based aerobic exercise and treadmill-based aerobic exercise on functional capacity, pulmonary function, and clinical outcomes in children with asthma. Participants aged 10-17 years with physician-diagnosed asthma will be randomly assigned to either a virtual reality-based exercise group or a treadmill exercise group. Both groups will undergo supervised exercise training sessions twice a week for 8 weeks. Primary outcome will be the 6-Minute Walk Test. Secondary outcomes include pulmonary function, respiratory muscle strength, asthma control, quality of life, and exercise adherence.

Participants needed: 30
Trial details
Age: 10-17Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Jul 21, 2026Locations: 1
Eligibility criteria

Children and adolescents aged between 10 and 17 years [+4]

Presence of orthopedic, neurological, cardiovascular, or systemic conditions lim... [+4]

Status: Recruiting

Determinant Factors in Excessive Gestational Weight Gain: Physical Activity, Nutritional Status, and Anxiety

This study aims to identify which of the following factors-physical activity level, nutritional status, or pregnancy-related anxiety-has the strongest influence on excessive gestational weight gain. Pregnant women in their third trimester who are being followed at Gebze Fatih State Hospital and meet the inclusion criteria will be referred to the Exercise Therapy Laboratory of the Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Bezmialem Vakıf University. After being informed about the study and providing written informed consent, participants will undergo a face-to-face assessment. Data will be collected prospectively using a demographic information form, the Pregnancy Physical Activity Questionnaire (PPAQ), a nutritional status assessment form, and a pregnancy-related anxiety questionnaire.

Participants needed: 150
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Jul 21, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Being in the 3rd trimester of pregnancy [+2]

High-risk pregnancy [+2]

Status: Not yet recruiting

Pelvic Floor Symptoms Across Menopausel Stages

The menopausal transition is associated with substantial hormonal alterations that may adversely affect lower urinary tract function, bowel function, and sexual health. Although these symptoms are common, few studies have comprehensively evaluated all three pelvic floor compartments across different menopausal stages. The aim of this study is to compare lower urinary tract symptoms, bowel symptoms, and female sexual function among women in the perimenopausal, early postmenopausal, and late postmenopausal stages. In addition, the relationship between menopausal stage and symptom severity will be investigated.

Participants needed: 180
Trial details
Age: 40-65Biological sex: FemaleType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Jul 9, 2026Locations: 1
Eligibility criteria

Female [+4]

Hormone replacement therapy within the previous 6 months [+8]

Status: Not yet recruiting

Synchronized Core-Pelvic Floor Activation in Urinary Incontinence

This study aims to investigate whether co-activation of the pelvic floor and core muscles improves treatment outcomes in individuals with urinary incontinence. Participants diagnosed with stress, or mixed urinary incontinence will undergo a 12-week pelvic floor physiotherapy program, with or without additional core muscle co-activation exercises. Changes in urinary incontinence severity, pelvic floor muscle function, core muscle activation, and quality of life will be evaluated.

Participants needed: 50
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Aged between 18 and 65 years [+3]

Pregnancy [+6]

Status: Not yet recruiting

Cognitive-Based Balance Rehabilitation in Parkinson's Disease: Virtual Reality vs. Dual Task

This prospective, randomized, single-blind, controlled clinical trial aims to evaluate and compare the efficacy of cognitive-based balance rehabilitation delivered via immersive Virtual Reality (VR) versus traditional Dual-Task Training (DTT) on balance, gait, cognitive functions, and quality of life in patients with Parkinson's Disease (PD). Postural instability and cognitive decline are hallmark features of progressive PD that significantly elevate fall risks and compromise daily independence, yet conventional pharmacological therapies offer limited effectiveness in restoring complex postural control. Given that motor and cognitive processes are intrinsically linked, this study addresses a critical gap in neurorehabilitation by investigating two contemporary modalities designed to challenge these systems simultaneously. A total of 34 participants diagnosed with PD (aged 40-80 years, Hoehn and Yahr stages I-III) will be randomly allocated to either the Dual-Task Group (DTG), receiving structured therapeutic exercises integrated with sequential cognitive tasks, or the Virtual Reality Group (VRG), engaging in an immersive balance program utilizing the Oculus Quest 2® headset with the FIT-XR application. Both groups will undergo an identical intervention protocol consisting of 45-minute supervised sessions, conducted twice weekly for 8 consecutive weeks during their pharmacological "on" phase. Standardized assessments will be performed by a blinded clinician at baseline and post-intervention (Week 8). The primary outcome measures will be dynamic balance and gait assessed through the Mini-Balance Evaluations Systems Test (Mini-BESTest) alongside global cognitive performance measured via the Montreal Cognitive Assessment (MoCA). Secondary outcomes will encompass objective posturographic indices using the Biodex Balance System, motor severity via the Unified Parkinson's Disease Rating Scale (UPDRS-III), freezing of gait, health-related quality of life, global perceived improvement, and potential cyber-sickness symptoms monitored through the Virtual Reality Sickness Questionnaire (VRSQ) to comprehensively determine the safety and comparative therapeutic value of these interventions.

Participants needed: 34
Trial details
Age: 40-80Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Jun 25, 2026
Eligibility criteria

Diagnosed with Parkinson's Disease by a neurologist. [+6]

Currently participating in another exercise or drug trial. [+4]

Status: Not yet recruiting

Telerehabilitation Versus Face-to-Face LSVT BIG in Individuals With Parkinson Disease

This prospective, randomized controlled trial will enroll 40 individuals with idiopathic PD (Hoehn \& Yahr stages 1-3, MoCA ≥21). Participants will be randomly assigned in a 1:1 ratio to either a telerehabilitation LSVT BIG group or a face-to-face LSVT BIG group, with randomization stratified by Hoehn \& Yahr stage using a computer-based block randomization system. Both groups will receive the standard LSVT BIG® protocol consisting of 16 sessions over four weeks (4 days/week, 1 hour/session). Treatment content will include maximal daily exercises, functional component tasks, "big" gait training, and individually tailored hierarchy tasks. The telerehabilitation group will receive all sessions via synchronous video conferencing under physiotherapist supervision, while the face-to-face group will receive sessions in a clinical setting. Both groups will be assigned home exercise programs in accordance with the LSVT BIG® protocol, and treatment adherence will be monitored throughout the study. Outcomes will be assessed at baseline, after 4 weeks of treatment, and at 6-month follow-up. Primary outcomes include postural stability and fall risk assessed with the Biodex Balance System (anterior-posterior stability index, mediolateral stability index, general stability index, fall risk index, limits of stability) and motor and non-motor symptom severity assessed with the MDS-UPDRS (Parts I, II, and III). Secondary outcomes include dynamic balance (Mini-BESTest), functional mobility (Timed Up and Go Test, 10-Meter Walk Test), quality of life (PDQ-39), depression (Beck Depression Inventory), sleep quality (Parkinson's Disease Sleep Scale), fatigue (Parkinson Fatigue Scale), cognitive function (MoCA), and treatment satisfaction (Global Rating of Change Scale).

Participants needed: 40
Trial details
Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Jun 11, 2026
Eligibility criteria

Diagnosis of idiopathic Parkinson's disease [+5]

Diagnosis of a neurological condition other than idiopathic Parkinson's disease [+7]

Status: Recruiting

Clinical Performance of Bioactive Bulk-Fill in Class II Restorations

This prospective split-mouth clinical study aims to compare the clinical performance of a bioactive bulk-fill composite with a conventional microhybrid composite in Class II posterior restorations. In each participant, two comparable Class II cavities will be treated using different restorative approaches. In the experimental condition, a bioactive bulk-fill composite (Activa BioACTIVE Bulk Flow) will be placed at the gingival base and covered with a microhybrid composite (Filtek Z250). In the control condition, restorations will be completed entirely with the microhybrid composite (Filtek Z250). Clinical performance will be evaluated according to FDI World Dental Federation criteria at baseline, 6 months, and 12 months. Primary outcomes include marginal adaptation, retention, and overall clinical success of the restorations. Secondary outcomes include surface properties and marginal staining. The split-mouth design allows direct intra-individual comparison, thereby minimizing inter-individual variability and increasing the reliability of the findings. The results of this study are expected to provide evidence on the effectiveness of bioactive bulk-fill composites in improving the clinical performance of posterior restorations.

Participants needed: 34
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Apr 23, 2026Locations: 1
Eligibility criteria

Adults aged between 18 and 50 years [+3]

Patients with systemic diseases affecting oral health [+4]

Status: Recruiting

Nigella Sativa Oil for Eczematous Otitis Externa

Eczematous otitis externa is a common inflammatory condition of the external auditory canal characterized by itching, discomfort, discharge, and pain. Topical corticosteroids are widely used for treatment; however, alternative therapies with fewer side effects are of increasing interest. This study aims to compare the efficacy of Nigella sativa (black seed) oil and mometasone furoate ear drops in the treatment of eczematous otitis externa. Nigella sativa is a natural product with known anti-inflammatory and antimicrobial properties. In this randomized, controlled clinical trial, adult patients with eczematous otitis externa will be assigned to receive either Nigella sativa oil or mometasone furoate ear drops for 10 days. Clinical symptoms and inflammatory findings will be evaluated at baseline and after treatment. The objective of this study is to determine whether Nigella sativa oil is an effective and safe alternative to topical corticosteroid therapy.

Participants needed: 85
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Apr 21, 2026Locations: 1
Eligibility criteria

Adult patients aged 18 years and older [+3]

Known hypersensitivity or allergic reaction to Nigella sativa oil or mometasone... [+5]

Status: Not yet recruiting

PULP SENSIBILITY AND MASSETER INHIBITORY REFLEX IN DIABETIC POLYNEUROPATHY

Accurate evaluation of dental pulp health is essential to avoid unnecessary endodontic treatments. In routine dental practice, pulp sensibility is commonly assessed using electric pulp testing and thermal (cold) testing. However, these tests depend on patient perception and may be influenced by various factors such as systemic diseases, nerve damage, anxiety, trauma, or medication use. Diabetic polyneuropathy is a common complication of diabetes mellitus and may alter peripheral nerve function, potentially affecting dental pulp sensibility test responses. This clinical study aims to evaluate how the severity of diabetic polyneuropathy influences dental pulp sensibility responses and masseter inhibitory reflex (MIR) parameters. The MIR is an objective neurophysiological reflex that allows quantitative assessment of trigeminal nerve function. In this study, individuals with mild diabetic polyneuropathy, severe diabetic polyneuropathy, and healthy controls will be evaluated. All participants will undergo electric pulp testing, cold testing, and MIR measurements using standardized protocols. The primary hypothesis of this study is that increasing severity of diabetic polyneuropathy leads to reduced dental pulp sensibility responses and altered MIR parameters compared to healthy individuals. It is further hypothesized that conventional pulp sensibility tests may produce false-negative results in patients with advanced neuropathy. The findings of this study are expected to contribute to more accurate endodontic diagnosis and improved understanding of orofacial neurophysiological changes in diabetic patients.

Participants needed: 108
Trial details
Age: 25-65Biological sex: AllType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Apr 3, 2026
Eligibility criteria

Diagnosis of diabetic polyneuropathy confirmed by a neurologist [+7]

History of chemotherapy, head and neck radiotherapy, or systemic conditions know... [+6]

Status: Not yet recruiting

Traction, Pressure, and Rapid Muscle Release (TPR) Technique During Intramuscular Injection: Effects on Pain and Patient Satisfaction

This study will be conducted to evaluate the effect of the Traction, Pressure, and Rapid Muscle Release (TPR) technique, an innovative method used during intramuscular vitamin B12 (cyanocobalamin) injections, on patients' pain and satisfaction levels compared with the conventional injection method.

Participants needed: 102
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Mar 30, 2026Locations: 1
Eligibility criteria

Voluntary participation in the study [+4]

Presence of a scar, burn, redness, hematoma, bruising, tenderness, or induration... [+7]

Status: Recruiting

Stress Ball Use During Cataract Surgery: Effects on Pain, Fear and Satisfaction

The aim of this study is to determine the effect of stress ball use during cataract surgery on patients' pain, fear, and satisfaction levels.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Mar 6, 2026Locations: 1
Eligibility criteria

Individuals aged 18 years or older, [+4]

Under 18 years of age, [+5]

Status: Not yet recruiting

Comparison of Virtual Reality-Based and Routine Preoperative Education on Surgical Anxiety and Salivary Cortisol

This randomized controlled pilot study aims to compare the effects of virtual reality-based preoperative education and routine preoperative education on surgical anxiety in patients undergoing lumbar disc surgery. In addition to evaluating psychological outcomes, the study will also compare psychometric anxiety assessments with a biological stress marker, salivary cortisol, to examine the relationship between subjective and physiological stress responses. Preoperative anxiety is common among surgical patients and may negatively influence both emotional well-being and physiological stress regulation. Virtual reality-based education may provide a more immersive and engaging learning experience compared to routine education, potentially reducing anxiety levels. Participants will be randomly assigned to either a virtual reality-based education group or a routine preoperative education group. Surgical anxiety will be assessed using validated psychometric measurement tools, and physiological stress response will be evaluated through salivary cortisol analysis. The study will further explore the concordance between psychometric findings and biological stress indicators. The results may contribute to the development of innovative, evidence-based nursing interventions and provide insight into the relationship between psychological and biological indicators of preoperative anxiety.

Participants needed: 56
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Mar 2, 2026
Eligibility criteria

Not listed

Status: Not yet recruiting

Association Between Child and Parental Stress and Bruxism in Children Aged 8-11 Years

This prospective observational case-control study aims to evaluate the association between perceived stress levels in children and their parents and the presence of clinically diagnosed bruxism in children aged 8-11 years. Children with bruxism and age-matched controls will be recruited from the Department of Pediatric Dentistry. Child perceived stress, parental perceived stress, parenting-related stress, and parental awareness of child stress/anxiety will be assessed using validated questionnaires. Associations between stress-related measures and bruxism status will be analyzed.

Participants needed: 100
Trial details
Age: 8-11Biological sex: AllType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Feb 25, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Assessment of Cognitive Function and Functional Performance in Patients With Type 2 Diabetes

Diabetes is a chronic metabolic disease that is becoming a growing public health problem worldwide, affecting people's lives in many ways. It is characterized by impaired carbohydrate, lipid, and protein metabolism associated with insufficient insulin secretion and/or reduced sensitivity to the metabolic effects of insulin.Along with diabetes, many complications may develop in affected individuals. Cognitive impairments are now also considered an important and common complication of diabetes.The aim of this study is to investigate the effects of cognitive function levels on functional capacity, balance, fear of falling, and quality of life in individuals with type 2 diabetes.In this context, participants' cognitive function levels will be assessed using the Mini-Mental State Examination and the Stroop Test. Functional capacity will be evaluated using the 6-Minute Walk Test. Balance performance will be assessed using the Biodex Balance System and the Four Square Step Test. Lower extremity muscle strength will be measured using a digital hand-held dynamometer and the 30-Second Sit-to-Stand Test. Fear of falling will be evaluated using the Falls Efficacy Scale-International (FES-I), the Functional Reach Test, and the Timed Up and Go (TUG) Test. Participants' quality of life will be assessed using the WHOQOL-BREF quality of life questionnaire.

Participants needed: 80
Trial details
Age: 40-65Biological sex: AllType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Feb 5, 2026Locations: 1
Eligibility criteria

Being between 40 and 65 years of age [+5]

Having a diagnosis of any neurological or psychiatric disorder (e.g., hemiplegia... [+6]

Status: Recruiting

Assesment of Ethnic Bias in an Artificial Intelligence Based Orthodontic Diagnosis System

This study explores how artificial intelligence (AI) can be used in orthodontics, which is the area of dentistry that focuses on correcting jaw and bite problems. AI is a computer technology that can learn from large amounts of data and then make predictions or decisions. It is already being tested in medicine and dentistry to help doctors and dentists diagnose conditions. For this study, the AI system was trained using photographs and X-rays from patients in Turkey. The system learned to recognize specific orthodontic skeletal malocclusions. After the training stage, the AI was tested in two groups: one group included Turkish patients whose records were not used in training, and the other group included patients from different ethnic backgrounds who were treated at a clinic in Belgium. This design allows researchers to see if the AI works equally well for people of different backgrounds. Only photographs and X-rays taken before orthodontic treatment are used in the study, and all data are anonymized so that no personal information is shared. The images must meet certain quality standards. For example the head must be in natural position, with no beards, scars, or previous orthodontic treatment that might affect the image. Patients who do not meet these criteria are not included. The AI program analyzes the profile photographs, prepares them for evaluation by adjusting and standardizing the images, and then tries to decide each patient has which malocclusion. The results from Turkish patients and patients from other ethnic groups are compared to see if the system makes fair and accurate decisions for everyone. The purpose of this study is not to test a new treatment, but to understand how well AI can recognize orthodontic problems in different populations. This information is important because AI systems are increasingly being used in healthcare, and they need to be fair and accurate for all patients, not just those from one group. By participating, patients help researchers learn whether AI in orthodontics is reliable across diverse communities. This knowledge can guide future improvements in AI technology, ensuring that it supports orthodontists in providing safe, equal, and effective care for everyone.

Participants needed: 5,000
Trial details
Age: 4+Biological sex: AllType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Dec 5, 2025Locations: 1
Eligibility criteria

Patients with lateral profile photographs taken before starting orthodontic trea... [+4]

Blurry missing or non standard profile photographs [+2]

Status: Recruiting

The Effect of Escape Room Method in Nursing Process Teaching

This study will be conducted to determine the effectiveness of education provided through the educational escape room method in nursing process teaching and to examine its effects on 4th-year nursing students' self-efficacy, teamwork, and anxiety.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Dec 2, 2025Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

An Artificial Intelligence Model for Intensive Care Length of Stay, Neurological Outcome and Costs Estimation After Cardiopulmonary Resuscitation: a Cohort Study.

The study aims to overview patients registered to Bezmialem Vakıf University Hospital Intensive Care Unit after successive cardiac arrest resuscitation from October 2010 to September 2025. The goal is to determine length of stay in reanimation, neurological clinical outcome and costs of these patients at discharge from the department. All these data is intended to be evaluated by artificial intelligence to evaluate a predictive model.

Participants needed: 5,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Oct 7, 2025
Eligibility criteria

age>18 years [+2]

age < 18 years [+2]

Status: Not yet recruiting

Acute Effects of Prolonged Walking on Hallux Valgus

Hallux valgus is a progressive foot deformity characterized by lateral deviation of the great toe and medial displacement of the first metatarsal head. While pain is a common symptom among individuals with HV, alterations in plantar pressure distribution and impaired balance are also frequently observed. These symptoms and biomechanical changes can negatively impact posture and gait mechanics. The aim of this study is to investigate the acute effects of prolonged walking on pain, balance, posture, and gait in individuals with hallux valgus deformity.

Participants needed: 32
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Sep 17, 2025Locations: 1
Eligibility criteria

Individuals aged between 18 and 55 years [+4]

History of previous foot or ankle surgery [+3]

Status: Recruiting

The Effect of Body Weight on Physical Activity Level, Functional Capacity, Balance, and Quality of Life in Individuals With Type 2 Diabetes Mellitus

This study aims to investigate the effects of body weight on physical activity level, functional capacity, balance, and quality of life in patients with type 2 diabetes mellitus (T2DM). A total of 50 volunteer patients who meet the inclusion criteria will be recruited from the Internal Medicine and Nutrition outpatient clinics of Bezmialem Vakıf University Hospital. Participants will be prospectively evaluated through face-to-face interviews. Assessments will include body composition analysis (Omron Body Composition Monitor), waist-to-hip ratio, lower extremity muscle strength (Muscle Hand-Held Dynamometer), grip strength (Hand Grip Dynamometer), physical activity level (International Physical Activity Questionnaire-Short Form), functional capacity (6-Minute Walk Test), balance (Biodex Balance System), clinical balance (Berg Balance Scale), and quality of life (Nottingham Health Profile). All statistical analyses will be performed using IBM SPSS Statistics 20. With this study, we aim to comprehensively evaluate multiple parameters in individuals with T2DM and investigate their interrelationships, thereby contributing to the current body of knowledge in the literature.

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Sep 3, 2025Locations: 1
Eligibility criteria

Having a diagnosis of Type 2 Diabetes Mellitus for at least 1 year [+5]

Presence of uncontrolled cardiovascular and pulmonary disease [+9]

Status: Not yet recruiting

Effect of Digital Physiotherapy Practice on Pulmonary Function, Muscle Strength, Quality of Life After Thoracic Surgery

Thoracic surgery is the primary intervention used in the treatment of diseases affecting the lungs, pleura, chest wall, and mediastinum. Postoperative changes occur in both lung functions and clinical symptoms due to the procedure itself and patient-related factors. After thoracic surgery, patients often experience reduced exercise tolerance and impaired respiratory functions, negatively affecting their participation in daily activities, functional levels, and quality of life. In open thoracotomies, the incision site, severed muscles, and the size of the incision can impact upper extremity and trunk functions. The aim of this study is to investigate the effects of physiotherapy applied through digital methods on respiratory functions, respiratory muscle strength, functional capacity, upper extremity muscle strength, and quality of life in patients who have undergone thoracic surgery.

Participants needed: 26
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Bezmialem Vakif UniversityUpdated: Aug 21, 2025
Eligibility criteria

Patients who underwent open thoracotomy [+3]

Pneumonectomy surgeries [+4]

Status: Recruiting

Metabolic Profiling of Saliva in Pregnancy and Periodontal Disease

This study aims to better understand how pregnancy affects the health of the gums and tissues that support the teeth. During pregnancy, hormone levels (like estrogen and progesterone) increase significantly. These hormonal changes can cause many changes in the body, including in the mouth. Some pregnant women may notice that their gums become swollen, red, or bleed more easily - this is called pregnancy gingivitis. It happens more often during the second and third trimesters and usually improves after birth. Even if a pregnant person has good oral hygiene, hormonal changes may still make the gums more sensitive to plaque and bacteria. Scientists believe that these changes in gum health are linked to how the body responds to hormones, bacteria in the mouth, and changes in the immune system. To explore this further, saliva samples will be collected from: * Pregnant women during their 1st, 2nd, and 3rd trimesters * The same women again 6-8 weeks after giving birth * A group of non-pregnant, healthy women as a comparison group The investigators will use a scientific method called untargeted metabolomics to study these saliva samples. This method helps looking at small substances (called metabolites) in saliva to see if there are any patterns related to pregnancy and gum health. The goal is to identify biological changes that happen during pregnancy and understand how they might affect the gums. This research will help improve early detection and prevention of gum problems during pregnancy in the future.

Participants needed: 30
Trial details
Age: 18-40Biological sex: FemaleType: ObservationalSponsor: Bezmialem Vakif UniversityUpdated: Jul 23, 2025Locations: 1Duration: 9 Months
Eligibility criteria

Age between 18 and 40 years [+10]

Use of anti-inflammatory or antimicrobial treatments in the past 3 months [+7]