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Clinical Trials in Turkey / NCT07465874
Starting soon Observational

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

NCT07465874 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-03-23
Last updated
2026-03-12

Condition(s) studied

Obstructive Sleep ApneaSleep Apnea

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Being between 18 and 65 years of age Having a diagnosis of obstructive sleep apnea (OSA) confirmed by polysomnography Having sufficient cognitive ability to understand and follow the test instructions Having adequate shoulder range of motion to elevate the upper extremities above head level for performing the 6PBRT Voluntarily agreeing to participate in the study and providing written informed consent Exclusion Criteria: * Presence of neurological diseases that may significantly affect upper extremity function (e.g., stroke, multiple sclerosis, peripheral neuropathy) Severe orthopedic conditions limiting upper extremity movement (e.g., advanced shoulder pathology, recent surgery, severe contracture) Unstable cardiopulmonary conditions (e.g., recent myocardial infarction, decompensated heart failure, uncontrolled arrhythmia, acute COPD/asthma exacerbation) Acute infection, febrile illness, or severe clinical exacerbation within the last 4 weeks Pain severe enough to interfere with the test or any clinical condition preventing the safe administration of the test

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Mardin Artuklu University Mardin Mardin

More Mardin Artuklu University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07465874 on ClinicalTrials.gov ↗ ← All trials in Turkey