Low-Cost Handgrip Dynamometer in Healthy Adults

July 28, 2025 updated by: Pelin Tiryaki, University of Yalova

Validity and Reliability a Low-cost Handgrip Dynamometer in Healthy Adults

The gold standard device for measuring grip strength is the Jamar® Hydraulic Hand Dynamometer. The Jamar® Hydraulic Hand Dynamometer is a high-priced device. It has an analog reading feature. The Jamar hydraulic hand dynamometer is recommended by the American Association of Hand Therapists and is considered the gold standard because of its high validity and reliability. Due to its cost, the use of this dynamometer is quite limited in certain countries and settings. However, there is a new version, the JAMAR Plus+, which has a digital reading feature. This version is even more expensive. In recent years, the use of less expensive dynamometers for measuring grip strength has become increasingly common in clinical settings and scientific research. In particular, the Camry Dynamometer, which is ten times cheaper, is frequently used. Despite its frequent use in scientific research, a review of the current literature has shown that the validity and reliability of the Camry has not been examined in healthy populations. Our study compares the Jamar® Hydraulic Hand Dynamometer, the gold standard device for measuring grip strength, with the lower cost and lighter handheld digital Camry dynamometer.

Study Overview

Status

Active, not recruiting

Study Type

Observational

Enrollment (Estimated)

177

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Yalova, Turkey
        • Yalova University
      • Yalova, Turkey, 77200
        • University of Yalova

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Healthy adults

Description

Inclusion Criteria:

  • Healty volunteers with 18-65 years

Exclusion Criteria:

  • Using any assistive device,
  • Having rheumatoid arthritis, gout, neuromuscular disease or any acute/chronic disease that may affect grip strength,
  • Pregnancy,
  • Previous subluxation, dislocation or fracture in the upper extremity,
  • Type 1 or Type 2 DM,
  • Unstable chronic and systemic diseases

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximum handgrip strength - Device 1
Time Frame: 7 days
Maximum grip strength is a measure of muscular strength or the maximum force/tension generated by one's forearm muscles.
7 days
Maximum handgrip strength - Device 2
Time Frame: 7 days
Maximum grip strength is a measure of muscular strength or the maximum force/tension generated by one's forearm muscles.
7 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
International Physical Activity Questionnaire - Short Form
Time Frame: Baseline
The purpose of the questionnaire is to provide common instruments that can be used to obtain internationally comparable data on health-related physical activity. The total score is grouped as inactive (<600 MET-min/week), minimally active (minimum 600 MET-min/week and <3000 MET-min/week) and active (>3000 MET-min/week).
Baseline
SBQ - Sedentary Behaviour Questionnaire
Time Frame: Baseline
The SBQ was designed to assess the amount of time spent doing 9 behaviors (watching television, playing computer/video games, sitting while listening to music, sitting and talking on the phone, doing paperwork or office work, sitting and reading, playing a musical instrument, doing arts and crafts, sitting and driving/riding in a car, bus, or train). The 9 items were completed separately for weekdays and weekend days.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Pelin Tiryaki, PhD, University of Yalova

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 16, 2025

Primary Completion (Actual)

July 28, 2025

Study Completion (Estimated)

August 30, 2025

Study Registration Dates

First Submitted

February 19, 2025

First Submitted That Met QC Criteria

February 19, 2025

First Posted (Actual)

February 25, 2025

Study Record Updates

Last Update Posted (Actual)

July 29, 2025

Last Update Submitted That Met QC Criteria

July 28, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2024/293

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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