Test-Retest Reliability of Grip Force Sense for Proprioception Assessment

NCT ID: NCT07334808

Last Updated: 2026-01-15

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 55 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2026-01-13
• Study Completion Date: 2026-12-19

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.

Detailed Description

Participants aged 18-24 who are willing to participate in the study will be included. The necessary demographic information will be obtained using a data form. Participants will be seated in a chair with back support. Participants will perform isometric grip tasks with their arms at their sides, elbows flexed at 90°, and wrists in a neutral position. Subsequently, to assess participants' grip force sense, they will be measured on how accurately they can perform the applied 'force reproduction tasks'. Participants will be subjected to three different target force levels (10%, 30%, and 50% MVIC). A total of 9 trials will be conducted, with three repetitions for each force level. Participants will perform these 9 trials in two separate sessions (Session 1 and Session 2). The sessions will be conducted 7 days apart, in the same laboratory environment and by the same researcher. This will allow for the assessment of the test-retest reliability of the grip force sense. Throughout this process, grip strength will be measured using a digital hand dynamometer. Force values will be observed via a digital monitor. Three different error types will be calculated from the data related to the force reproduction task: (1) AE (Absolute Error), (2) CE (Constant Error), and (3) VE (Variable Error). Minimum-maximum values, mean and standard deviation will be used in the evaluation of continuous data, while frequency distributions and percentages will be used for categorical data. The data of the study will be analysed using IBM SPSS Statistics version 21.1 (IBM Corp., Armonk, NY) statistical package programmes. In all analyses, p<0.05 will be considered statistically significant.

Conditions

Healthy Volunteers

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

All Participants

Healthy volunteers. All participants will be assessed at baseline and re-assessed after a 1-week interval to determine test-retest reliability.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Age 18-24 years
• Volunteering to participate

Exclusion Criteria

• Having a history of hand surgery
• Having any active pathology or pain complaints in the hand

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 24 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Kutahya Health Sciences University

OTHER

Sponsor Role: lead

Responsible Party

Emrah Afsar

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Emrah Afsar, Phd

Role: PRINCIPAL_INVESTIGATOR

Kutahya Health Science University

Locations

Kutahya Health Science University

Kütahya, , Turkey (Türkiye)

Site Status: RECRUITING

Countries

Turkey (Türkiye)

Central Contacts

Emrah Afsar, Phd

Role: CONTACT

emrah.afsar@ksbu.edu.tr

5062527008

Ayse Kocak Sezgin, Phd

Role: CONTACT

ayse.kocaksezgin@ksbu.edu.tr

+90 5072243706

Facility Contacts

Emrah Afsar, Phd

Role: primary

emrah.afsar@ksbu.edu.tr

5062527008

Other Identifiers

2025-a

Identifier Type: -

Identifier Source: org_study_id