- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06845072
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
Conditions
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
-
-
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Yalova, Turkey
- Yalova University
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Yalova, Turkey, 77200
- University of Yalova
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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
|
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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.
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Baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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.
General Publications
- Leong DP, Teo KK, Rangarajan S, Lopez-Jaramillo P, Avezum A Jr, Orlandini A, Seron P, Ahmed SH, Rosengren A, Kelishadi R, Rahman O, Swaminathan S, Iqbal R, Gupta R, Lear SA, Oguz A, Yusoff K, Zatonska K, Chifamba J, Igumbor E, Mohan V, Anjana RM, Gu H, Li W, Yusuf S; Prospective Urban Rural Epidemiology (PURE) Study investigators. Prognostic value of grip strength: findings from the Prospective Urban Rural Epidemiology (PURE) study. Lancet. 2015 Jul 18;386(9990):266-73. doi: 10.1016/S0140-6736(14)62000-6. Epub 2015 May 13.
- Cildan Uysal S, Tonak HA, Kitis A. Validity, reliability and test-retest study of Grip strength measurement in two positions with two dynamometers: Jamar(R) Plus and K-Force(R) Grip. Hand Surg Rehabil. 2022 Jun;41(3):305-310. doi: 10.1016/j.hansur.2022.02.007. Epub 2022 Mar 10.
- Guerra RS, Amaral TF, Sousa AS, Fonseca I, Pichel F, Restivo MT. Comparison of Jamar and Bodygrip Dynamometers for Handgrip Strength Measurement. J Strength Cond Res. 2017 Jul;31(7):1931-1940. doi: 10.1519/JSC.0000000000001666.
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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