Association Between Hand-Eye Coordination and Handgrip Strength in Children Post-Healing of DRGF

June 17, 2025 updated by: Muhammad Naveed Babur, Superior University

Association Between Hand-Eye Coordination and Handgrip Strength in Children Post-Healing of Distal Radius Greenstick Fractures: A Cross-Sectional Study

The study investigates whether hand-eye coordination is related to handgrip strength in children (aged 5-12 years) after they have healed from distal radius greenstick fractures. This is important because both strength and coordination are crucial for a child's full functional recovery after such fractures.

Cross-sectional analytical study Orthopedic and physiotherapy departments in Lahore 84 children (convenience sampling)

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

84

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

  • Pakistan
    • Punjab
      • Lahore, Punjab, Pakistan
        • Superior University CRC

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

  • Child

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Handgrip Strength and Hand-Eye Coordination Assessment in the Association Between Hand-Eye Coordination and Handgrip Strength in Children Post-Healing of Distal Radius Greenstick Fractures: A Cross-Sectional Study

Description

Inclusion Criteria:

  • Children aged 5-12 years
  • Radiologically confirmed healed distal radius greenstick fractures
  • Ability to perform handgrip and hand-eye coordination tests
  • Parental consent and child assent

Exclusion Criteria:

  • Acute pain or swelling at the time of testing
  • Current medications affecting bone/muscle function
  • Neuromuscular or developmental disorders
  • History of previous upper limb fractures or surgeries

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
Handgrip Strength and Hand-Eye Coordination Assessment
Combination product: Handgrip Strength and Hand-Eye Coordination Assessment
Children underwent standardized testing to assess functional recovery post-healing of distal radius greenstick fractures.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Beery-Buktenica Developmental Test of Visual-Motor Integration
Time Frame: 6 Month

(Beery VMI): Provides standard scores and percentile ranks:

129: Very High (2% of age group)

120-129: High (7%)

110-119: Above Average (16%)

90-109: Average (50%)

80-89: Below Average (16%)

70-79: Low (7%)

<70: Very Low (2%)
6 Month

Collaborators and Investigators

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

Sponsor

Superior University

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)

March 4, 2025

Primary Completion (Actual)

June 1, 2025

Study Completion (Estimated)

September 30, 2025

Study Registration Dates

First Submitted

June 17, 2025

First Submitted That Met QC Criteria

June 17, 2025

First Posted (Estimated)

June 25, 2025

Study Record Updates

Last Update Posted (Estimated)

June 25, 2025

Last Update Submitted That Met QC Criteria

June 17, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DPT/Batch-Fall20/1014

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

Yes

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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