Validity and Reliability of the Six-minute Peg Board and Ring Test in Patients With Rheumatoid Arthritis

NCT ID: NCT06753851

Last Updated: 2025-12-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-01-26

Study Completion Date

2025-11-03

Brief Summary

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The aim of the study was to evaluate the validity and reliability of 6-PBRT in patients with rheumatoid arthritis and to determine the applicability of the test for this population.

Detailed Description

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Rheumatoid arthritis (RA) is a systemic, inflammatory disease that causes pain and joint involvement. Pain, loss of range of motion, and decreased muscle strength lead to loss of function in patients with RA. Hand grip and generalized muscle weakness in patients cause decreased upper extremity functions. A study found that the upper extremity functional capacity of RA patients was lower than that of healthy individuals. In routine evaluations of rheumatoid arthritis patients, rough and fine grip strength measurements are made, but these measurements do not provide sufficient information about upper extremity functional exercise capacity. Rehabilitation programs aim to improve upper extremity function, therefore, valid and reliable methods are needed to determine upper extremity function in RA patients and to measure the effectiveness of rehabilitation programs. The six-minute peg board and ring test (6-PBRT) is a valid, reliable, useful, practical and easy-to-apply test that evaluates upper extremity endurance without support in patients with chronic obstructive pulmonary disease and asthma and in healthy individuals (5-7). Studies have determined that the total number of rings in 6-PBRT has a positive relationship with upper extremity daily living activities in COPD and asthma patients. Six-PBRT is frequently used in the evaluation of upper extremity exercise capacity and endurance without support and in determining the effectiveness of rehabilitation programs. The validity and reliability of 6-PBRT, which is used in the evaluation of functional upper extremity exercise capacity in different diseases, has not been investigated in patients with RA. The arm ergometer test is also a gold standard method used to evaluate upper extremity exercise capacity. Therefore, it was planned to use the arm ergometer test as a criterion measure for the validity of 6-PBRT in our study. The aim of this study was to evaluate the validity and reliability of 6-PBRT in patients with rheumatoid arthritis and to determine the applicability of the test for this patient population.

Conditions

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Rheumatoid Arthritis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Rheumatoid arthritis group

All evaluations in the study will be completed on two separate days. First, demographic information, medical history and clinical findings of the patients will be recorded. On the first day, handgrip strength, DASH questionnaire and first 6-PBRT and arm ergometer test will be performed. The first 6-PBRT will be performed on the patients at least 30 minutes before the arm ergometer test and the patients will rest between the two tests. One week later, the same expert physiotherapist who performed the evaluations will perform the second 6-PBRT on the patients for reliability analysis.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Patients diagnosed with rheumatoid arthritis,
* Ages of between 18-75 years,
* Patients who volunteer to participate in the study will be included in the study.

Exclusion Criteria

* Serious cardiopulmonary, neurological, neuromuscular, orthopedic and other systemic diseases or other diseases affecting physical functions,
* Participated in a planned exercise program in the last three months,
* Cognitive impairment that will cause difficulty in understanding and following exercise test instructions,
* Contraindications to exercise testing or exercise training according to the American Sports Medicine Association will not be included in the study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kirsehir Ahi Evran Universitesi

OTHER

Sponsor Role lead

Responsible Party

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Başak KAVALCI KOL

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Başak KAVALCI KOL, PhD, PT

Role: PRINCIPAL_INVESTIGATOR

Kirsehir Ahi Evran Universitesi

Merve FIRAT, PhD, PT

Role: STUDY_CHAIR

Kirsehir Ahi Evran Universitesi

Figen TUNCAY, Prof. Dr., MD

Role: STUDY_CHAIR

Kirsehir Ahi Evran Universitesi

Locations

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Kırşehir Ahi Evran University, 63 / 5.000 Physical Therapy and Rehabilitation Center, Cardiopulmonary Unit

Kırşehir, Merkez, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Bearne LM, Coomer AF, Hurley MV. Upper limb sensorimotor function and functional performance in patients with rheumatoid arthritis. Disabil Rehabil. 2007 Jul 15;29(13):1035-9. doi: 10.1080/09638280600929128.

Reference Type RESULT
PMID: 17612988 (View on PubMed)

Takeda K, Kawasaki Y, Yoshida K, Nishida Y, Harada T, Yamaguchi K, Ito S, Hashimoto K, Matsumoto S, Yamasaki A, Igishi T, Shimizu E. The 6-minute pegboard and ring test is correlated with upper extremity activity of daily living in chronic obstructive pulmonary disease. Int J Chron Obstruct Pulmon Dis. 2013;8:347-51. doi: 10.2147/COPD.S45081. Epub 2013 Jul 23.

Reference Type RESULT
PMID: 23901268 (View on PubMed)

Lima VP, Almeida FD, Janaudis-Ferreira T, Carmona B, Ribeiro-Samora GA, Velloso M. Reference values for the six-minute pegboard and ring test in healthy adults in Brazil. J Bras Pneumol. 2018 May-Jun;44(3):190-194. doi: 10.1590/S1806-37562017000000388.

Reference Type RESULT
PMID: 30043884 (View on PubMed)

Other Identifiers

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AhiEvranU524

Identifier Type: -

Identifier Source: org_study_id

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