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CompletedNCT07422064Updated Jun 17, 2026

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

An observational study in Parkinson's Disease (PD), Functional Capacity and Upper Extremity Function, sponsored by Sanko University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 40 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-06-17.

Sponsored by Sanko University · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
47
Ages
40 Years to 75 Years
Sex
All
01

Study summary

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.

Read the detailed description

Parkinson's disease (PD) primarily arises from the progressive degeneration of the nigrostriatal dopaminergic pathway and neurons in the substantia nigra pars compacta, which aggregate in the form of Lewy bodies or Lewy neurites. PD is the second most common neurodegenerative disease after Alzheimer's disease, with a prevalence of 0.3% in the general population and 1-3% in the population over 65 years of age. As the disease progresses, the decrease in dopamine levels leads to resting tremor, bradykinesia, rigidity, impaired reflexes, depression, anxiety, emotional changes, cognitive impairment, difficulty swallowing, chewing and speaking, blank facial expressions, urinary problems, constipation, fatigue and sleep problems. Although the course and rate of progression of Parkinson's disease, which has an insidious onset, vary from patient to patient, the symptoms progress over the years in an extremely slow but gradually increasing manner. The asymmetric onset of the disease is very typical, and motor symptoms usually begin with resting tremor. Asymmetry in symptoms is maintained throughout the course of the disease, and bradykinesia develops to varying degrees in each patient. While there is a decrease in movement speed and amplitude (bradykinesia) in the early stages of the disease, it can progress over time and turn into akinesia. Initially, only the distal muscles are affected (micrographia, limited finger movements), but over time, all muscle groups become involved, and patients may eventually become unable to perform activities of daily living. We believe that the six-minute pegboard ring test may be valid and reliable in these individuals. If found to be valid and reliable, its use is recommended for the assessment of individuals diagnosed with Parkinson's disease. Assessments of patients referred from the SANKO University Hospital 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. Subsequently, patients will be grouped using the Hoehn-Yahr Staging Scale. Vital signs such as blood pressure, saturation, and pulse will be checked. 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 Arm, Shoulder, and Hand Questionnaire (DASH). The assessments will be conducted by Fzt. 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.

02

Conditions studied

  • Parkinson's Disease (PD)
  • Functional Capacity
  • Upper Extremity Function
  • Validity and Safety

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Keywords

  • Parkinson's Disease
  • Functional Capacity
  • Upper Extremity Function
  • Validity and Reliability
03

In context

Parkinson Disease

4,488 studies on the registry are indexed under Parkinson Disease; 1,083 are open to participants now.

This study's enrollment of 47 is below the median of 96 across 1,057 observational studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

Sanko University is the lead sponsor of 49 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients diagnosed with Parkinson's disease at the SANKO University Sani Konukoğlu Application and Research Hospital Neurology Outpatient Clinic

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • Having a neurological disorder other than Parkinson's disease
  • Having a visual impairment
  • Having dyskinesia severe enough to interfere with the test
05

Study design

Observational model
Other
Time perspective
Other
Enrollment
47 participants (actual)
Target follow-up
3 Months
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. Nine-Hole Peg Test

    It is a simple, timed test used to assess an individual's fine motor skills, hand-eye coordination, and upper extremity function. The test board has 9 small holes. There are 9 small pegs in front of the person. The participant uses one hand to place the pegs into the holes one by one, then removes them again. This process should be completed in the shortest possible time. It is performed separately for each hand. The time is measured for evaluation.

    Time frame: 1 year

  2. Blood Pressure

    As our study involves the assessment of functional capacity and upper extremity function, these parameters will be measured during the test, as the individual's physiological state must remain stable

    Time frame: 1 year

  3. Manual muscle test device

    Muscle strength (right foot dorsi flexion, left foot dorsi flexion, right foot plantar flexion, left foot plantar flexion) will be measured with Commander Echo brand manual muscle test device. The participant will be asked to resist the resistance as much as possible and the maximum force will be recorded. After the participants are informed, 1 trial will be performed. Muscle strength measurement will be repeated 3 times and the average value will be recorded in kilograms.

    Time frame: 1 year

  4. Fatigue Severity Scale

    On the nine-item scale, the highest score is 63 and the lowest score is 9. An increase in the fatigue severity scale score indicates a higher level of fatigue.

    Time frame: 1 year

  5. Wrist, Shoulder, and Hand Problems Survey(DASH)

    This is a self-report questionnaire developed to assess functional limitations and pain levels in the arm, shoulder, and hand regions of individuals. It consists of a total of 30 questions. It inquires about the person's daily living activities, symptoms, and functionality over the past week. Subheadings: daily living activities (carrying objects, writing, combing hair, etc.), symptom assessment (pain, stiffness, weakness), social life and psychological impact, work/activity limitations. Each question is rated from 1 (no difficulty) to 5 (great difficulty/unable to perform). Score range: 0-100. 0 points: No limitations. 100 points: Maximum limitations and problems. At least 27 questions must be answered.

    Time frame: 1 year

  6. Hoehn and Yahr Staging Scale

    It is a 5-level classification system developed in 1967 and used to determine the clinical stage of Parkinson's disease based on motor symptoms. It is frequently used to determine the progression of the disease and support treatment planning. The stages are as follows: Stage 1: Only unilateral symptoms Stage 2: Bilateral symptoms, no balance issues Stage 3: Mild postural imbalance, still independent Stage 4: Significant motor impairment, requires some assistance Stage 5: Wheelchair-bound or bedridden

    Time frame: 1 year

07

Study locations

1 site
  • Sanko Unıversıty
    Gaziantep, 27090, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Undecided — will be decided when the study is completed

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07422064
Lead sponsor
Sanko University
Responsible party
Hakan Polat (pyhsiotherapy and rehabilitation, Phd PT, Sanko University) — Principal investigator
First posted
Feb 19, 2026
Start date
Nov 1, 2025
Primary completion
Dec 15, 2025
Completion
Feb 6, 2026
Last update
Jun 17, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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