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Grip StrengthNCT07735195

Tyrannosaurus Flex: Finding the "Fair-ly Normal" Grip

A study testing Dinomometer in people with Grip Strength and Hand Strength, run by University of Minnesota at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The purpose of this study is to evaluate the performance of the Dinomometer and establish normative data to inform clinical standards and benchmarks for therapeutic practice. This is a cross-sectional study designed to collect normative grip strength data from a large sample of the general population in Minnesota. Read more about this study

Who is it for?
Ages 2 to 12 yearsHealthy volunteers can take part
Conditions the study is for
Grip Strength, Hand Strength
What is being tested?
Dinomometer
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
600 participants
Where
1 siteUnited States
Study dates
6 Sep 2026to 31 Aug 2028
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 2 to 12 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Children between the ages of 2-12 year old who demonstrate participation interest and provide informed consent and assent (when appropriate).

Who cannot join

  • Presence of a known musculoskeletal, neurological, or neuromuscular condition affecting upper limb strength or function (including, but not limited to, cerebral palsy, brachial plexus injury, muscular dystrophy, etc.)
  • Diagnosis of a systemic condition affecting the musculoskeletal or nervous system
  • Previous hand, wrist, or upper limb surgery
  • History of hand, wrist, or upper limb trauma
  • Current pain in either hand or upper limb
  • Persons unable to follow standardized commands when presented to them in English

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Corey McGee, PhD, MS, OTR/L, CHT, FAOTA contact

612-626-5645

mcge0062@umn.edu

United States1 site, 1 recruiting
  • UOM State Fair- 1367 Cosgrove Street, Falcon Heights

    Minneapolis, Minnesota, 55108

    Corey McGee, PhD, MS, 612-626-5645, mcge0062@umn.edu

    Recruiting

Other trials in United States

About this study

The purpose of this study is to evaluate the performance of the Dinomometer and establish normative data to inform clinical standards and benchmarks for therapeutic practice.

This is a cross-sectional study designed to collect normative grip strength data from a large sample of the general population in Minnesota. Participants will primarily be recruited from attendees of the Minnesota State Fair. Grip strength will be measured using the Dinomometer, a non-invasive handheld grip strength measurement device.

The study should take approximately 10-15 minutes to complete for each participant including enrollment and completion of study procedures. Follow-up is not required.

Read the detailed description

This is a cross-sectional study designed to collect normative grip strength data from a large sample of the general population in Minnesota. Participants will be primarily recruited from attendees of the Minnesota State Fair, a community event that draws a broad cross-section of individuals across age, sex, height and weight, providing an opportunity to collect normative data that is representative of the general population. The goal of this study is to establish reference values to inform clinical benchmarks for therapeutic use of the Dinomometer.

A designated research booth will be set up at the Minnesota State Fair with signage inviting interested fairgoers to participate in the study. A trained research team member will provide interested participants with a brief explanation of the study. Written informed consent will then be obtained from a parent or guardian on behalf of minor participants, with assent obtained from children as appropriate.

Following consent, the participant will be directed to a trained research team member who will collect demographic information including sex, age, race, ethnicity, county of residence, height, weight, and hand circumference and will log this information into a pre-prepared case report form administered via iPad. No personal identifiers such as names will be collected.

The participant will then be seated comfortably in a chair with the arm adducted and the elbow gently positioned at a 90-degree angle if possible. The research team member will record whether this position was achieved and maintained. Grip strength will be measured using the Dinomometer, a non-invasive handheld grip strength measurement device. Grip strength will be measured on each hand, with short rest breaks and alternation between hands to mitigate the effects of fatigue. Hand size will be measured by taking a circumferential measurement in centimeters of each hand using a standard plasticized dressmaker's tape laid across the distal palmar crease.

The following data will be collected from each participant: age, sex, height, weight, race, ethnicity, county of residence, hand size, hand dominance, grip strength measurements, and whether the standard testing position was achieved and maintained. All data will be recorded in the case report form on an iPad. The Dinomometer is the only device required for participation in this study. It is a non-invasive measurement tool and no drugs or additional investigational agents are required for participation.

The study should take approximately 10-15 minutes to complete for each participant including enrollment and completion of study procedures. Follow-up is not required.

Being tested
Dinomometer
Keywords
Dinomometer, Grip strength, Pediatric grip strength, Hand strength, Normative data, Reference values, Children, Occupational therapy, Minnesota State Fair

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • DinomometerDevice

    Also called Handheld grip strength measurement device

    The investigational device being evaluated in this study is the Dinomometer, a handheld grip strength measurement device designed for use in pediatric populations. The Dinomometer will be used to collect grip strength measurements from participants at the Minnesota State Fair. No drugs, biologics, or additional investigational agents are involved in this study.

Study groups in NCT07735195
Study groupRoleWhat they receive
Dinomometer Grip Strength AssessmentExperimentalParticipants will complete grip strength measurements using the Dinomometer, a non-invasive handheld grip strength measurement device. Grip strength will be measured on each hand, with short rest breaks and alternation between hands to mitigate the effects of fatigue.
Receives: Device: Dinomometer

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Collection of normative grip strength data using the Dinomometer

    The primary outcome is the collection of normative grip strength data from a large sample of the general population in Minnesota using the Dinomometer. These data will be used to establish reference values and benchmarks to inform clinical interpretation of Dinomometer measurements in therapeutic settings.

    Measured: During a single study visit lasting approximately 10-15 minutes

Secondary outcomes (1)
  1. Grip strength variability across demographic subgroups

    Secondary outcomes include the characterization of grip strength variability across demographic subgroups, including age, sex, height and weight. These data will inform the development of stratified normative reference values to support clinician decision-making across a range of patient populations.

    Measured: During a single study visit lasting approximately 10-15 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jul 2026
  2. Study start6 Sep 2026
  3. Primary completion31 Aug 2028 (estimated)
  4. Study completion31 Aug 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Model description
This is a cross-sectional study designed to collect normative grip strength data from a large sample of the general population in Minnesota.
Masking
None (open label)
Enrolment
600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07735195
Sponsor's protocol ID
STUDY00028771
Status last verified
Oct 2026
First submitted
20 Jul 2026
Last updated
7 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes

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