Assessment of Motor Adaptation in Precision Grip Performance of Children

December 11, 2024 updated by: National Cheng-Kung University Hospital

Assessment of Motor Adaptation in Precision Grip Performance of Children: a Kinetic Analysis of Responsive Grip Behavior

Preterm children usually suffer from mild hand motor performance, however, the problem are rarely detected in time. Identifying the pathology causing deficits in sensorimotor control of a hand helps the occupational therapist to determine appropriate clinical decision-making for intervention. Well-motor performance requires complete sensorimotor control. Understanding hand sensorimotor control mechanism and its neural control can help clinicians find the reason behind hand motor deficits. The analysis of motion adaptation of the precision pinch behavior in the perturbing environment has been regarded as a clinically meaningful tool for evaluating sensorimotor control of a hand, especially for the complex anatomical structure of bone and tendon. The motor adaptation analysis for the precision grip behavior can provide the temporal and spatial parameters of dynamic grip force adjustment. Therefore, the exploration of motor adjustment can provide in-depth understanding of the neural mechanisms that lead to impairment of motor function and skill acquisition of a child, which can assist clinical occupational therapist in identifying the cause and severity of impairment of children's hand skills and provide appropriate strategies and types of treatment. The recent research on children's motor adaptation focuses on the discussion of the efficiency of motor adaptation in unfamiliar or disturbing task situations. Thus, the first purpose of this research is to develop an easy-to-detect apparatus to detect the adjustment efficiency of a responsive grip behavior of children in a disturbing pinch-lifting task and to construct the reliability of its evaluation. The second purpose of the research is to understand the correlation between the efficiency of children's reactive pinch performance adjustment and the results of traditional evaluation of fine motor development scale and sensorimotor control assessments. The third purpose of the research is to analyze the difference in motor adjustment of a precision pinch performance at different ages of preschool children. The fourth purpose is to compare the efficiency of motor adaptation in preterm and term children. In addition, preterm birth is often accompanied by white matter abnormalities and affects future hand motor performance. Investigating white matter imaging markers for predicting motor adaptation can help early detection of problems. Therefore, the fifth objective was to explore whether specific white matter imaging markers can predict the efficiency of reactive motor adaptation.

Study Overview

Study Type

Observational

Enrollment (Actual)

65

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

      • Tainan, Taiwan, 704
        • National Cheng-Kung University Hospital

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

2 years to 39 years (Child, Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

healthy adults: 20-39 years old term children: 24-60 months preterm children: 24-48 months

Description

Inclusion Criteria:

  1. Must be able to do reach-to-grasp performance
  2. Intact comprehension ability

Exclusion Criteria:

  1. Diagnosis of cerebral palsy and other genetic or congenital damage
  2. Bone and nerve damage in the upper limbs in the past year
  3. Un-correctable problems of vision or hearing impairment

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
group of preterm and term children
group 1: preterm children group 2: term children
white matter imaging markers
group of different ages of preschool children
group 1: children with age of 25 months-36 months group 2: children with age of 37 months-48 months group 3: children with age of 49 months-60 months

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
responsive grip behavior
Time Frame: up to 2 years
amplitude of pinch force development or adaptation to perturbation
up to 2 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Bayley Scales of Infant and Toddler Development, Third Edition
Time Frame: up to 2 years
for diagnosing developmental delays in early childhood
up to 2 years
Peabody Developmental Motor Scales, Second Edition
Time Frame: up to 2 years
measure interrelated motor abilities of children from birth through age 5 years of age
up to 2 years
Tuning Fork 128 Hz
Time Frame: up to 2 years
measure vibration sense
up to 2 years
Box and blocks test
Time Frame: up to 2 years
measure upper limb coordination
up to 2 years
Semmes-Weinstein monofilament test
Time Frame: up to 2 years
measure touch-pressure sense
up to 2 years

Collaborators and Investigators

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

January 12, 2023

Primary Completion (Actual)

September 9, 2024

Study Completion (Actual)

September 12, 2024

Study Registration Dates

First Submitted

October 5, 2022

First Submitted That Met QC Criteria

October 6, 2022

First Posted (Actual)

October 10, 2022

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 11, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • B-BR-110-072

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

Clinical Trials on Diffusion tensor imaging

Subscribe