Actively Recruiting
Validity and Reliability of the 6-minute Pegboard and Ring Test in Measuring Upper Arm Function for Overweight and Obese Adults
Led by Kirsehir Ahi Evran Universitesi · Updated on 2024-12-19
24
Participants Needed
1
Research Sites
50 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the validity and reliability of the 6-minute pegboard and ring test to assess upper extremity function in adults who are overweight or obese. The study focuses on understanding how well this test measures arm exercise capacity, exercise capacity, hand grip strength, and muscle endurance in this population. Participants in this study will undergo the 6-minute pegboard and ring test, which is designed to assess upper limb function. The study does not mention additional treatments or interventions but focuses on evaluating this specific physical test. During the study, participants' arm exercise capacity, exercise capacity, hand grip strength, and muscle endurance will be measured on the first day. These assessments will help determine the test's effectiveness in measuring upper extremity function in overweight and obese adults. The total duration and follow-up details are not specified.
CONDITIONS
Official Title
The 6-minute Pegboard and Ring Test in Overweight and Obese Individuals
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Body mass index 6 25 kg/m2
- Volunteering for the study
You will not qualify if you...
- Having uncontrolled hypertension or diabetes mellitus
- Having comorbidities that may affect physical functions
- Not cooperating with the tests to be performed
- Having liver disease, kidney disease, cancer, lung diseases, serious cardiomyopathies, or neurological diseases
- Being pregnant
- Having a history of bariatric surgery
- Having contraindications to exercise testing
AI-Screening
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Trial Site Locations
Total: 1 location
1
Kirsehir Ahi Evran University
Kırşehir, Turkey (Türkiye)
Actively Recruiting
Research Team
M
Merve Firat
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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