Test-Retest Reliability of Grip Force Sense for Proprioception Assessment
1 other identifier
observational
55
1 country
1
Brief Summary
The aim of this study is to investigate the test-retest reliability of the grip force sense, a component of proprioception, using a dynamometer that is easily accessible and usable in a clinical setting. This provides an accessible assessment method for research in the field of proprioception.
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 Jan 2026
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
First Submitted
Initial submission to the registry
December 31, 2025
CompletedFirst Posted
Study publicly available on registry
January 12, 2026
CompletedStudy Start
First participant enrolled
January 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 12, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 19, 2026
January 15, 2026
January 1, 2026
11 months
December 31, 2025
January 13, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Absolute Error (AE)
Absolute Error (AE) represents the absolute difference between the target force and the reproduced force, without regard to direction. It reflects the overall accuracy of the force reproduction task.
Baseline and 1 week
Constant Error (CE)
Constant Error (CE) represents the directional difference between the target force and the reproduced force. It indicates the participant's directional bias (overshooting or undershooting the target).
Baseline and 1 week
Variable Error (VE)
Variable Error (VE) represents the variability or consistency of the participant's performance across trials, regardless of the target. It reflects the consistency of force reproduction.
Baseline and 1 week
Study Arms (1)
All Participants
Healthy volunteers. All participants will be assessed at baseline and re-assessed after a 1-week interval to determine test-retest reliability.
Eligibility Criteria
The study population consisted of healthy volunteers aged between 18 and 24 years without any history of previous hand surgery or presence of active pathology/pain in the hand.
You may qualify if:
- Age 18-24 years
- Volunteering to participate
You may not qualify if:
- Having a history of hand surgery
- Having any active pathology or pain complaints in the hand
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kutahya Health Science University
Kütahya, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Emrah Afsar, Phd
Kutahya Health Science University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
December 31, 2025
First Posted
January 12, 2026
Study Start
January 13, 2026
Primary Completion (Estimated)
December 12, 2026
Study Completion (Estimated)
December 19, 2026
Last Updated
January 15, 2026
Record last verified: 2026-01