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

Validity and Reliability of the 6-Minute Pegboard and Ring Test (6PBRT) in Adults With Obstructive Sleep Apnea: A Polysomnography-Based Methodological Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07465874
Enrollment
80
Registered
2026-03-12
Start date
2026-03-23
Completion date
2026-11-15
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstructive Sleep Apnea, Sleep Apnea

Keywords

6-Minute Pegboard and Ring Test, Upper Extremity Functional Capacity, Polysomnography, Obstructive Sleep Apnea, Functional Performance

Brief 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.

Detailed description

Obstructive sleep apnea (OSA) is characterized by repetitive episodes of upper airway obstruction during sleep resulting in intermittent hypoxia, sleep fragmentation, and increased sympathetic activity. These physiological disturbances may negatively affect physical performance, daily functioning, and exercise tolerance. Although previous studies have investigated balance, gait, and overall physical performance in individuals with OSA, upper extremity functional capacity has received limited attention. The 6-Minute Pegboard and Ring Test (6PBRT) is a functional performance test that evaluates upper extremity endurance during unsupported arm activity. The test has been used primarily in patients with chronic respiratory diseases to assess functional limitation during activities involving arm elevation. However, the validity and reliability of the 6PBRT have not been investigated in individuals with OSA. This observational methodological study aims to evaluate the validity and reliability of the 6PBRT in adults diagnosed with OSA using polysomnography. Participants diagnosed with OSA will be recruited from the sleep center of Mardin Training and Research Hospital. Demographic and clinical data including age, sex, body mass index, and comorbidities will be recorded. Polysomnographic parameters including apnea-hypopnea index (AHI), oxygen desaturation index (ODI), minimum oxygen saturation (SpO₂), and the percentage of sleep time with oxygen saturation below 90% (T90) will be collected from medical records. Upper extremity functional capacity will be assessed using the 6PBRT. Participants will perform the test according to standardized procedures. Test-retest reliability will be evaluated by repeating the test under similar conditions. In addition, clinical scales including the Epworth Sleepiness Scale (ESS) and the Functional Outcomes of Sleep Questionnaire (FOSQ) will be administered. The validity of the 6PBRT will be investigated by examining its relationship with polysomnographic parameters and clinical scales. Reliability will be evaluated using test-retest analysis and intraclass correlation coefficients. The results of this study will provide important information regarding the measurement properties of the 6PBRT in individuals with OSA and may support its use as a practical tool for assessing upper extremity functional capacity in clinical practice.

Interventions

None listed

Sponsors

Mardin Artuklu University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
6-Minute Pegboard and Ring Test (6PBRT) ScoreBaselineUpper extremity functional capacity assessed using the 6-Minute Pegboard and Ring Test. The outcome will be the total number of rings moved during the 6-minute test.

Secondary

MeasureTime frameDescription
Epworth Sleepiness Scale (ESS)BaselineDaytime sleepiness will be assessed using the Epworth Sleepiness Scale (score range 0-24).
Functional Outcomes of Sleep Questionnaire (FOSQ)BaselineSleep-related functional status will be assessed using the Functional Outcomes of Sleep Questionnaire.
Hand Grip StrengthBaselineHand grip strength will be measured using a hand dynamometer to evaluate upper extremity muscle strength.
Polysomnography ParametersBaselineRelationship between 6PBRT performance and polysomnographic parameters including Apnea-Hypopnea Index (AHI), Oxygen Desaturation Index (ODI), minimum oxygen saturation (SpO₂), and percentage of sleep time with oxygen saturation below 90% (T90).
Fatigue Severity Scale (FSS)BaselineFatigue severity will be assessed using the Fatigue Severity Scale (score range 1-7). Higher scores indicate greater fatigue severity.
Test-Retest Reliability of the 6PBRTWithin 7 daysReliability of the 6PBRT will be evaluated by repeating the test under the same conditions and calculating intraclass correlation coefficients.

Countries

Turkey (Türkiye)

Contacts

CONTACTengin ramazanoğlu, Assistant Professor
enginramazanoglu@artuklu.edu.tr+905334889447

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026