Clinical trials

7

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

Condition / disease
Location
Status: Recruiting

Functional Capacity Differences in Knee Osteoarthritis With Similar Pain Severity

People with knee osteoarthritis may have similar levels of pain but very different abilities to walk, rise from a chair, and perform daily activities. This study aims to examine the factors associated with these differences in functional capacity among patients with similar knee pain severity. Adults with radiographic knee osteoarthritis and an average knee pain level of 4-6 on a 0-10 scale will be included. During a single study visit, participants will complete questionnaires about physical function, central sensitization-related symptoms, and physical activity. They will also perform a 10-meter walk test, a 30-second chair stand test, and the Timed Up and Go test. Self-reported physical function will be assessed using the function subscale of the Western Ontario and McMaster Universities Osteoarthritis Index. Participants with better and poorer function will be compared, and the clinical factors independently associated with functional capacity will be examined. No treatment or intervention will be assigned as part of this study.

Participants needed: 120
Trial details
Age: 40-75Biological sex: AllType: ObservationalSponsor: Mardin Artuklu UniversityUpdated: Oct 9, 2026Locations: 1
Eligibility criteria

Age 40-75 years [+5]

Kellgren-Lawrence grade 1 or 4 knee osteoarthritis [+6]

Status: Recruiting

Is Central Sensitization a Prognostic Indicator in Chronic Nonspecific Low Back Pain?

This observational study will examine whether signs of increased sensitivity in the nervous system at the beginning of the study are associated with short-term clinical outcomes in adults with chronic nonspecific low back pain. Approximately 180 participants will complete questionnaires about central sensitization, disability, pain, anxiety, and depression at the beginning of the study. After 6 weeks, disability, pain, and the participant's overall perception of change will be assessed again. The researchers will evaluate whether the initial level of central sensitization is associated with meaningful improvement in disability and perceived treatment benefit. Participants will not be assigned to a treatment as part of this study and will continue to receive routine clinical care.

Participants needed: 180
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Mardin Artuklu UniversityUpdated: Sep 17, 2026Locations: 1
Eligibility criteria

Adults aged 18 to 65 years [+3]

Progressive neurological deficit [+7]

Status: Recruiting

Daily Symptom Fluctuations and Functional Impact in Fibromyalgia

Fibromyalgia is a chronic condition that commonly causes widespread pain, fatigue, and difficulty in daily activities. These symptoms may change from day to day, even when their average severity is similar. This study aims to examine whether daily changes in pain and fatigue are related to functional impact in adults with fibromyalgia. Participants will complete clinical questionnaires at the first visit and record their pain and fatigue levels for seven days. Sleep quality and perceived control over symptoms will also be recorded. No treatment or additional medical procedure will be given as part of the study.

Participants needed: 150
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Mardin Artuklu UniversityUpdated: Sep 17, 2026Locations: 1
Eligibility criteria

Diagnosis of fibromyalgia according to the 2016 American College of Rheumatology... [+3]

Active inflammatory rheumatic disease [+6]

Status: Not yet recruiting

Daytime vs Evening Rehabilitation in Lumbar Disc Herniation Patients at High Risk for Obstructive Sleep Apnea

Lumbar disc herniation is a common musculoskeletal condition that negatively affects quality of life, physical function, and daily activities. Previous studies have shown that individuals with lumbar disc herniation often experience poor sleep quality, which is closely related to pain severity and functional limitations. In addition, a bidirectional relationship exists between chronic pain and sleep disturbances, where poor sleep can increase pain perception, and pain can further impair sleep. Obstructive sleep apnea (OSA) is a common sleep-related breathing disorder associated with reduced sleep quality, daytime dysfunction, and adverse health outcomes. The STOP-Bang questionnaire (Snoring, Tiredness, Observed apnea, high blood Pressure, Body mass index, Age, Neck circumference, and Gender) is a widely used and practical screening tool to identify individuals at high risk for OSA in clinical settings. Physiotherapy and rehabilitation programs are commonly used in the conservative management of lumbar disc herniation and have been shown to improve pain and functional outcomes. However, the effect of the timing of rehabilitation (daytime versus evening) on sleep-related outcomes has not been sufficiently investigated. Considering that circadian rhythms influence pain perception, physiological processes, and sleep regulation, the timing of rehabilitation interventions may play an important role in clinical outcomes. Therefore, this randomized controlled trial aims to investigate the effects of daytime versus evening rehabilitation programs on sleep quality and daytime sleepiness in patients with lumbar disc herniation who are at high risk for obstructive sleep apnea.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Mardin Artuklu UniversityUpdated: Apr 13, 2026
Eligibility criteria

Individuals aged 18-65 years [+7]

Presence of sequestrated disc herniation or cauda equina compression confirmed b... [+16]

Status: Not yet recruiting

Validity and Reliability of the 6-Minute Pegboard and Ring Test (6PBRT) in Adults With Obstructive Sleep Apnea Syndrome

Obstructive sleep apnea (OSA) is a common sleep-related breathing disorder characterized by recurrent upper airway obstruction during sleep, leading to intermittent hypoxia and sleep fragmentation. In addition to its well-known cardiometabolic consequences, OSA may negatively affect functional capacity and daily activity performance. However, upper extremity functional capacity in individuals with OSA has not been adequately evaluated. The 6-Minute Pegboard and Ring Test (6PBRT) is a functional test designed to assess upper extremity functional capacity during unsupported arm activity. Although the test has been widely used in respiratory diseases, its measurement properties have not yet been evaluated in patients with OSA. The aim of this study is to investigate the validity and reliability of the 6PBRT in adults diagnosed with obstructive sleep apnea using polysomnography. Participants with OSA will undergo polysomnographic evaluation and complete the 6PBRT. Test-retest reliability will be assessed by repeating the test under the same conditions. The relationship between 6PBRT performance and polysomnographic parameters (AHI, ODI, minimum SpO₂ and T90) will also be examined. In addition, associations between 6PBRT performance and clinical scales such as the Epworth Sleepiness Scale and Functional Outcomes of Sleep Questionnaire will be analyzed. The findings of this study are expected to provide evidence regarding the measurement properties of the 6PBRT in individuals with OSA and contribute to the clinical assessment of upper extremity functional capacity in this population.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Mardin Artuklu UniversityUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Being between 18 and 65 years of age

Presence of neurological diseases that may significantly affect upper extremity...

Status: Recruiting

Mixed Reality Training for Teaching Cervical Effacement and Dilation

The aim of this educational research is to determine whether a mixed reality-based training program is effective in teaching midwifery students how to assess cervical effacement and dilation. The study also examines the impact of mixed reality on students' cognitive load, sense of presence, and midwifery professional perception. The main questions the study seeks to answer are: Does mixed reality training reduce students' cognitive load? Does mixed reality increase the students' sense of presence? How does mixed reality-based training influence students' professional perception of midwifery? Do students who receive mixed reality training perform better in assessing cervical effacement and dilation on real pregnant women compared with the control group?

Participants needed: 90
Trial details
Age: 18-35Biological sex: FemaleType: InterventionalSponsor: Mardin Artuklu UniversityUpdated: Nov 20, 2025Locations: 1
Eligibility criteria

Enrolled in the Midwifery Department at Mardin Artuklu University, [+5]

Individuals who are graduates of health vocational high schools, [+2]

Status: Recruiting

The Effectiveness of Basic Body Awareness Therapy in Individuals With Pes Planus

This study investigates whether adding Basic Body Awareness Therapy (BBAT) to Short Foot Exercises (SFE) improves pes planus, balance, and body awareness in adults with flexible pes planus. Fifty participants aged 18-45 will be randomly assigned to either a BBAT + SFE group or an SFE-only control group. The interventions will last eight weeks with supervised sessions twice weekly and additional home exercises. Outcomes will be measured before, after, and two months post-intervention.

Participants needed: 50
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Mardin Artuklu UniversityUpdated: Nov 17, 2025Locations: 1
Eligibility criteria

Aged 18-45 years [+2]

Pain in lower extremity joints [+10]