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NCT07422064Completed

Validity and Reliability of the Six-Minute Pegboard Ring Test in Individuals With Parkinson's Disease

Validity and Reliability of the Six-Minute Pegboard Ring Test for Assessing Functional Capacity and Upper Extremity Function in Individuals With Parkinson's Disease

Source: ClinicalTrials.gov · Last updated 17 Jun 2026

Brief summary (registry, in English)

Parkinson's patients who volunteer to participate in the study will be included. Parkinson's patients participating in the study will be referred from the SANKO University Hospital Neurology Outpatient Clinic. The assessments of patients referred from the Neurology Outpatient Clinic will be conducted at the SANKO University Physiotherapy and Rehabilitation Department Research Laboratory. The socio-demographic information of the included patients will be collected. Patients will then be grouped using the Hoehn-Yahr Staging Scale. Vital signs such as blood pressure, saturation, and pulse will be measured. Upper extremity muscle strength will be assessed using a dynamometer. Upper extremity performance will be assessed using the Nine-Hole Peg Test. The patient's fatigue will be assessed using the Fatigue Severity Scale, and upper extremity disability will be assessed using the Disability of the Arm, Shoulder, and Hand (DASH) questionnaire. The assessments will be conducted by Physiotherapist Rüveyda GÜRDAL.Except for the six-minute pegboard ring test, the other tests will evaluate the parameters required for an individual's upper extremity function. These parameters are balance, muscle strength, and fine motor skills. The six-minute pegboard ring test will be reassessed one week later by a different physiotherapist at the SANKO University Department of Physiotherapy and Rehabilitation Research Laboratory.

Status (registry)
Completed
Study type
Observational
Enrollment
47 (actual)
First submitted
11 Feb 2026
Start date
1 Nov 2025
Primary completion date
15 Dec 2025
Lead sponsor
Sanko University
NCT number
NCT07422064

What you commit to

  • Study type: Observational
  • Participants enrolled: 47
  • From 1 Nov 2025 to the primary completion date, 15 Dec 2025
  • 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.

Other illness

  • Having a neurological disorder other than Parkinson's disease
  • Having a visual impairment

Other

  • Having dyskinesia severe enough to interfere with the test

Who the study is looking for

  • Having been diagnosed with Parkinson's disease
  • Being over 35 years of age
  • Not having changed medications in the last 2 months
  • Being able to walk with or without assistance
  • Volunteering to participate in the study

Age in the registry: 40 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
Sanko Unıversıty
Coordinator of this site? Confirm its status
GaziantepTurkey (Türkiye)Unknown status

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