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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorMardin Artuklu University

About this trial

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 criteria

This trial accepts healthy volunteers

Qualifiers

Being between 18 and 65 years of age

Disqualifiers

Presence of neurological diseases that may significantly affect upper extremity function (e.g., stroke, multiple sclerosis, peripheral neuropathy)

Trial population

Adults diagnosed with obstructive sleep apnea based on polysomnography who are followed in the Sleep Center of Mardin Training and Research Hospital will be included in the study. Participants will be classified into mild, moderate, and severe obstructive sleep apnea groups according to the apnea-hypopnea index (AHI). In addition, age- and sex-matched healthy individuals without obstructive sleep apnea will be recruited as a control group.

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

80 Participants
are grouped into 4 trial groups
Group A: Mild Obstructive Sleep Apnea
Group B: Moderate Obstructive Sleep Apnea
Group C: Severe Obstructive Sleep Apnea
Group D: Healthy Control

Trial outcomes

Primary outcomes

1

6-Minute Pegboard and Ring Test (6PBRT) Score

Upper 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.

Time frame
Baseline

Secondary outcomes

1

Test-Retest Reliability of the 6PBRT

Reliability of the 6PBRT will be evaluated by repeating the test under the same conditions and calculating intraclass correlation coefficients.

Time frame
Within 7 days
2

Hand Grip Strength

Hand grip strength will be measured using a hand dynamometer to evaluate upper extremity muscle strength.

Time frame
Baseline
3

Functional Outcomes of Sleep Questionnaire (FOSQ)

Sleep-related functional status will be assessed using the Functional Outcomes of Sleep Questionnaire.

Time frame
Baseline
4

Epworth Sleepiness Scale (ESS)

Daytime sleepiness will be assessed using the Epworth Sleepiness Scale (score range 0-24).

Time frame
Baseline

Other outcomes

Sponsors and contacts

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