The Validity and Reliability of an Improved Paper Grasping Test for Parkinson's Disease
1 other identifier
observational
40
1 country
1
Brief Summary
The study will include volunteer patients diagnosed with Parkinson's disease who applied to the Neurology Outpatient Clinic at SANKO University Sani Konukoğlu Application and Research Hospital. Patients who meet the inclusion criteria will be evaluated by Dr. Hakan Polat and Physiotherapist Fatma Yılmaz in the application laboratory of the Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, SANKO University. The assessment form prepared by the researchers will be completed face-to-face with the patients. First, demographic information and disease-related data (duration since Parkinson's diagnosis, disease stage, affected side, etc.) will be recorded. The Mini-BESTest will be used to evaluate balance and gait. The muscle strength of the ankle plantar flexor and dorsiflexor muscles will be assessed using a manual muscle testing device, and quality of life will be measured with the Parkinson's Disease Questionnaire-39 (PDQ-39). Since fall problems in patients may be related to balance impairments, lower limb muscle weakness, and reduced quality of life, these parameters will also be evaluated. Therefore, in this study, while examining the validity and reliability of the modified paper grip test in individuals with Parkinson's disease, its correlation with these parameters will also be investigated. Before administering the tests, participants will receive a practical explanation of how the tests are performed and will be allowed to rest prior to assessment. The tests will be administered in the following order: first, the paper grip test by Dr. Hakan Polat, followed by the Mini-BESTest, assessment of ankle plantar and dorsiflexor muscle strength, and evaluation of quality of life. One week after the initial assessment, only the paper grip test will be re-administered by Physiotherapist Fatma Yılmaz in the same environment. This approach will minimize the effect of environmental factors on the patients' performance.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Aug 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 12, 2026
CompletedFirst Submitted
Initial submission to the registry
February 25, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 25, 2026
CompletedFirst Posted
Study publicly available on registry
August 19, 2026
CompletedAugust 19, 2026
February 1, 2026
5 months
February 25, 2026
August 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
mini best test
1\. Mini Best Test Description: This is one of the clinical tests used to assess walking and balance. It consists of four sub-parameters: preparatory movement, reactive postural control, sensory orientation, and dynamic walking, comprising a total of 14 items. It is a test scored out of a total of 28 points, taking an average of 10-15 minutes to complete. A high score indicates high function.
Measured once, at baseline (Session 1)
Manual muscle testing device
2\. Manual muscle testing device Description: muscle strength (right foot dorsiflexion, left foot dorsiflexion, right foot plantar flexion, left foot plantar flexion) will be measured using the Commander Echo brand manual muscle testing device. The participant will be a
Measured once, at baseline (Session 1)
Enhanced Paper Grasping Test
Description: During measurement, participants will sit in a calm environment on a chair without armrests, with their feet and knees at a 90-degree angle, and their upper limbs comfortably placed alongside their torso. This test involves
Baseline (Session 1) and 1 week later (Session 2)
Eligibility Criteria
parkinson
You may qualify if:
- Individuals who voluntarily agree to participate in the study -
You may not qualify if:
- Individuals who have taken any medication affecting walking ability within the last month or who have experienced an orthopedic injury within the last month
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sanko Universitylead
Study Sites (1)
Sanko Unıversıty
Gaziantep, Gaziantep, 27090, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physiotherapy and Rehabilitation Department, Assistant Professor
Study Record Dates
First Submitted
February 25, 2026
First Posted
August 19, 2026
Study Start
August 10, 2025
Primary Completion
January 12, 2026
Study Completion
June 25, 2026
Last Updated
August 19, 2026
Record last verified: 2026-02