Validity of the 6-Minute Pegboard and Ring Test in Parkinson's Patients

NCT ID: NCT06482502

Last Updated: 2025-03-07

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

RECRUITING

Total Enrollment

34 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-05-20

Study Completion Date

2025-12-31

Brief Summary

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Tests used to assess upper extremity endurance in Parkinson\'s patients are limited. This study aimed to investigate whether the 6-Minute Pegboard and Ring Test (6-MPRT), which has been validated in many respiratory disease groups in previous studies, is an endurance assessment battery that can also be used in Parkinson\'s patients. 6-MPRT, Weight Lifting Test, and 30-Second Arm Curl Test will be applied in the assessments. Assessments will be made twice on the same day by two different evaluators, 1 hour apart. After the first evaluation, the patient will be called for the second time 2 days later, and the same procedure will be repeated.

Detailed Description

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Conditions

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Parkinson Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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6-MPRT Group

There is 1 group in the study. All assessments are made on the same group.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Hoehn \& Yahr staging ≤3 points,
* Individuals who have not undergone a rehabilitation program of at least 20 days in the last 6 months,
* Those with full upper extremity shoulder flexion and abduction active joint range of motion.

Exclusion Criteria

* Those with severe heart disease such as heart failure, cardiac arrhythmia, hypertension,
* People with any orthopedic problem that will affect the upper extremity,
* Having a secondary neurological disease diagnosis,
* Having vision impairment that may affect measurement methods (not corrected by glasses),
* Having a cognitive disease that may cause difficulty in following the researchers\' commands,
* Those who had changes in their medical use during the test (dose increase/decrease, drug change
Minimum Eligible Age

45 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Emre Şenocak

OTHER

Sponsor Role lead

Responsible Party

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Emre Şenocak

Research Assisstant

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Murat Emirzeoğlu, PhD

Role: STUDY_CHAIR

Karadeniz Technical University

Adem Aktürk, PhD

Role: STUDY_CHAIR

İstanbul Gelişim University

Tuğba Eyigürbüz, PhD

Role: STUDY_CHAIR

Bağcılar Education and Research Hospital

Locations

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İstanbul Medilife Beylikdüzü Hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Emre Şenocak, PhD

Role: CONTACT

+90 553 569 56 92

Facility Contacts

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Call Center

Role: primary

+90 (212) 866 80 80

Adem Aktürk, PhD

Role: backup

+90 533 310 23 15

Other Identifiers

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2024/77

Identifier Type: -

Identifier Source: org_study_id

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