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NCT06482502Recruiting

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

Investigation of the Validity and Reliability of the 6-Minute Pegboard and Ring Test in Parkinson's Patients for Upper Extremity Endurance Assessments

Source: ClinicalTrials.gov · Last updated 7 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
34 (estimated)
First submitted
26 Jun 2024
Start date
20 May 2024
Primary completion date
31 Aug 2024
Lead sponsor
Emre Şenocak
NCT number
NCT06482502

What you commit to

  • Study type: Observational
  • Planned participants: 34
  • From 20 May 2024 to the primary completion date, 31 Aug 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Those who had changes in their medical use during the test (dose increase/decrease, drug change

Other illness

  • Those with severe heart disease such as heart failure, cardiac arrhythmia, hypertension,
  • 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,

Other

  • People with any orthopedic problem that will affect the upper extremity,

Who the study is looking for

  • 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.

Age in the registry: 45 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
İstanbul Medilife Beylikdüzü Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Recruiting

This page is information, not medical advice. Discuss any trial with your doctor.