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NCT Number: NCT07334808

Test-Retest Reliability of Grip Force Sense for Proprioception Assessment

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.

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Key information

Conditions

Age range

18 year–24 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Kutahya Health Science University

Kütahya, Turkey (Türkiye)

Location status: Recruiting

Location contact

Emrah Afsar, Phd

CONTACT

[email protected]

5062527008

Emrah Afsar, Phd

PRINCIPAL_INVESTIGATOR

Esila Bağdatlı, MSc

SUB_INVESTIGATOR

Zeynep Sena Namaz, MSc

SUB_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Absolute Error (AE)

    Time frame: Baseline and 1 week

    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.

  2. Constant Error (CE)

    Time frame: Baseline and 1 week

    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).

  3. Variable Error (VE)

    Time frame: Baseline and 1 week

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Ayse Kocak Sezgin, Phd

CONTACT

[email protected]

+90 5072243706

Emrah Afsar, Phd

CONTACT

[email protected]

5062527008

Sponsors and collaborators

Lead sponsor

Kutahya Health Sciences University

Other

Registry information

Official study title

Test-Retest Reliability of Grip Force Sense for Proprioception Assessment in Healthy Participants

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 12, 2026
Registry last updated
Jan 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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