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CompletedNCT04174729Updated Dec 3, 2019

System for Quantifying the Functional Strength of the Grip and Pinch Movements

An interventional study of handgrip strength and Door handle device in Hand Injuries and Disorders, sponsored by University of Mogi das Cruzes. Completed at 1 site in Brazil. Open to participants aged 20 Years to 39 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-12-03.

Sponsored by University of Mogi das Cruzes · Not applicable, Interventional, and Diagnostic

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Aug 2019, registered Nov 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
20 Years to 39 Years
Sex
All
01

Study summary

This study developed a system to quantify the functional strength of young adults without motor impairment during grip and pinch movement. Making it possible to know the accuracy of the value of these strength, the range of motion performed and whether the grip force was maintained throughout the range of motion. In addition to checking the functionality, reliability and reproducibility of the system.

Read the detailed description

Quantifying grip and grip movement is essential as it allows for a basis in upper limb functionality. However, when there is access, it causes changes in the hands and changes the motor in relation to the force and range of motion, or generates changes in activities of daily living. Thus, a system with 5 devices, where each one the devices were prints in three-dimensional, and instrumented with force sensor for static-dynamic force analysis e potentiometer for analysis range of motion, during the execution of movements cylindrical grip, spherical grip, hook grip, pulp-pulp pinch, and pulp- side pinch in different activities of daily living. Elaborated a data storage interface through MATLAB® software that allows recording the data of each device. For the system functionality tests, 30 volunteers were selected for both sexes, young adults between 20 and 39 years old, students of the Physiotherapy and Graduate courses of the University of Mogi das Cruzes. The tests are divided into two sessions and are repeated after 7 days of the first test

02

Conditions studied

  • Hand Injuries and Disorders

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03

In context

Hand Injuries

108 studies on the registry are indexed under Hand Injuries; 31 are open to participants now.

This study's enrollment of 30 is below the median of 56 across 84 interventional studies indexed under Hand Injuries.

Browse Hand Injuries studies →

Lead sponsor

University of Mogi das Cruzes is the lead sponsor of 16 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 39 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • only right-handed individuals,
  • male and female,
  • have preserved cognitive functions,
  • absence of neurological disorder
  • who present minimum grip strength by the Jamar ® dynamometer, in the age group of 20-29 years men 45.08 ± 0.67 kg and women of 27.2 ± 0.46 kg, who present minimum grip strength by the dynamometer Jamar ®, aged 30 to 39 years old men 46.05 ± 0.47 kg and women 28.0 ± 0.39 kg, using the mean minus the standard deviation.

Exclusion criteria

Exclusion Criteria:

  • Injury to upper limbs such as amputation, recent surgery (6 months), fractures, bruising, pain and musculoskeletal disorders.
  • Do not accept to participate in the survey.
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Hand strength

    The tests were performed in two sessions lasting 1 hour each. The volunteers used the devices: door handle, tap, door pull handle, switch and door key to quantify hand strength. The tests were performed in two sessions lasting 1 hour each. The volunteers used the devices: door handle, tap, door pull handle, switch and door key to quantify hand strength. In the first session, the volunteers performed the movements 3 times in each device of daily living activities with the right limb, with a 1-minute rest interval between the 3 measurements. The entire procedure performed in the session was repeated again after 30 minutes to verify the reliability and reproducibility of the Intra-evaluator test. The Inter-rater test was repeated after 7 days by the second rater to analyze reliability between the rater.

    Device: handgrip strength · Device: Door handle device · Device: Tap device · Device: Door pull handle · Device: Linear Switch device · Device: Door Key device

Interventions

  • Devicehandgrip strength

    First, the hand measurements of each volunteer were evaluated, followed by the measurement of handgrip strength using the Jamar® dynamometer. And later the tests were performed using the system that contains the 5 devices to quantify the hand strength.

    Also known as: Jamar dynamometer

  • DeviceDoor handle device

    To evaluate the cylindrical grip movement, a door handle was used, which evaluated the full force in the range of motion.

  • DeviceTap device

    To evaluate the spherical grip movement, a tap was used, which evaluated the full force in the range of motion.

  • DeviceDoor pull handle

    To assess the hook grip movement, a door pull handle was used, which assessed the full force in the range of motion

  • DeviceLinear Switch device

    To evaluate the pulp-pulp pinch movement, a switch was used, which evaluated the full force in the movement of the movement.

  • DeviceDoor Key device

    To assess the pulp-side pinch movement, a door key was used, which evaluated the full force in the range of motion.

06

What researchers measure

Primary outcomes

  1. Strength device

    The strength of the cylindrical grip movement was quantified through the door handle device, the spherical grip strength through the tap device, the hook grip strength through the vertical door pull handle, the pulp-pulp pinch strength through the linear switch device and the pulp-side pinch strength through the key device. The test was quantified 3 times with a 1 minute interval between each test and the force throughout the range of motion. Unit of measure: newton (N).

    Time frame: 15 minutes

Secondary outcomes

  1. Range of motion in angle

    The test measured the range of motion of the door handle device, the tap device, door pull handle device and the door key device, 3 times with 1 minute interval for each test, in which all range of motion was measured from its start until its end. Unit of measure: Angle (º).

    Time frame: 15 minutes

  2. Range of motion millimeter

    The test measured the range of motion in a linear switch device 3 times with a 1 minute interval for each test, in which all of the range of motion was measured from its start until its end. Unit measurement: millimeter (mm).

    Time frame: 15 minutes

Other outcomes

  1. Anthropometric variables

    The anthropometric measurement of the right hand was performed using an analog caliper, as it is an important parameter for functional evaluation, as it was of the following anatomical parts: total length of the hand (wrist crease to middle finger tip), longitudinal length of the palm from the hand (wrist crease to the proximal crease of the middle finger) and transverse length of the palm (lateral to medial line of the metacarpophalangeal muscles). Unit of measure: millimeter (mm)

    Time frame: 5 minutes

  2. Dynamometer Jamar Strength

    To make the sample more homogeneous, the Jamar ® dynamometer was used to measure grip strength maximum contraction for 3 seconds. A single measurement was performed. Unit of measure: kilogram - force (kgf).

    Time frame: 1 minute

07

Study locations

1 site
  • Silvia Regina Matos da Silva Boschi
    Mogi das Cruzes, São Paulo 08780-911, Brazil
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 3, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04174729
Lead sponsor
University of Mogi das Cruzes
Responsible party
Terigi Augusto Scardovelli (Principal Investigator, University of Mogi das Cruzes) — Principal investigator
First posted
Nov 22, 2019
Start date
Aug 5, 2019
Primary completion
Sep 9, 2019
Completion
Oct 29, 2019
Last update
Dec 3, 2019

Study contacts

Silvia R Boschi, PhD
principal investigator · University of Mogi das Cruzes

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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