Testing the 6-minute Pegboard Ring Test for obese individuals
Validity and Reliability of the 6-minute Pegboard Ring Test in Obese Individuals
This study is testing a new physical test to see how well it measures endurance in obese individuals.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Selcuk University Academic / other |
| Locations | 1 site (Konya, Selcuklu) |
| Trial ID | NCT06590584 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the validity and reliability of the 6-minute Pegboard Ring Test (6PBRT) specifically in obese individuals. Participants will undergo the test twice, with a one-hour rest period in between, during which various physiological parameters such as dyspnea, fatigue, muscle oxygenation, heart rate, and blood pressure will be monitored. The study will include 50 participants with a BMI of 30 kg/m² or higher, and data will be analyzed using statistical methods to assess the reliability of the test results. The goal is to provide a non-invasive assessment tool for evaluating upper extremity endurance in obese patients.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and over with a BMI of 30 kg/m² or higher who can ambulate independently.
Not a fit: Patients who are pregnant, have serious chronic conditions, or are on anti-obesity medications may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a reliable and valid tool for assessing exercise endurance in obese individuals, potentially leading to better management of obesity-related health issues.
How similar studies have performed: While the specific application of the 6PBRT in obese individuals is novel, similar studies have shown success in using exercise tests to evaluate physical capabilities in various populations.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * BMI value of 30 kg/m2 and above, * Ability to ambulate, * Being 18 years of age and above, * Being a volunteer. Exclusion Criteria: * Use of anti-obesity medication, * Pregnancy, * Latent autoimmune diabetes, * Chronic renal failure, * Active or serious infections, * Liver failure, * Recent major cardiovascular events, * Unstable angina, * Heart failure (NYHA III-IV) * Respiratory failure, cardiac arrhythmias, neoplastic diseases, and neurological or musculoskeletal disorders that limit testing.
Where this trial is running
Konya, Selcuklu
- Selcuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation — Konya, Selcuklu, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Mehmet K ALTUNOK, PHD(c) in PT
- Email: mehmetkaan.altunok@selcuk.edu.tr
- Phone: 5558175133
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.