The 6-minute Pegboard and Ring Test in Overweight and Obese Individuals

December 16, 2024 updated by: Merve Firat, Kirsehir Ahi Evran Universitesi

Validity and Reliability of the 6-minute Pegboard and Ring Test in Assessing Upper Extremity Function in Overweight and Obese Individuals

The aim of our study is to investigate the validity and reliability of the 6-minute pegboard and ring test in overweight and obese individuals.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

24

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Overweight and obese individuals will be included in the study.

Description

Inclusion Criteria:

  • Body mass index ≥ 25 kg/m2
  • Volunteering for the study

Exclusion Criteria:

  • Having uncontrolled hypertension, diabetes mellitus
  • Having comorbidities that may affect physical functions
  • Failure to cooperate with tests to be performed
  • Liver disease, kidney disease, cancer, lung diseases and serious cardiomyopathies, neurological diseases
  • Pregnancy
  • Having a history of bariatric surgery
  • Presence of contraindications to exercise testing

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Overweight and obese individuals

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle endurance
Time Frame: 1st day
30 second push-up test will be used, and total number will be recorded.
1st day
Arm exercise capacity
Time Frame: 1st day
It will be assessed by 6 minute pegboard and ring test.
1st day
Exercise capacity
Time Frame: 1st day
It will be assessed by 6 minute walk test.
1st day
Hand grip strength
Time Frame: 1st day
Will be measured using a hang grip dynamometer.
1st day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Upper extremity functional status
Time Frame: 1st day
Upper extremity functional status will be assessed with the Upper Extremity Functional Index. This index consists of 20 questions, and the lowest possible score is 0 and the highest score is 80. Higher scores indicate better functional status.
1st day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Kirsehir Ahi Evran Universitesi

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 11, 2024

Primary Completion (Estimated)

May 1, 2025

Study Completion (Estimated)

December 1, 2025

Study Registration Dates

First Submitted

December 16, 2024

First Submitted That Met QC Criteria

December 16, 2024

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 16, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2024-20/173

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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