Effect of Constraint Induced Movement Therapy on Burned Dominant Hand Function (CIMT)

November 25, 2024 updated by: Ahmed Elbadri Farouk Ahmed, Cairo University
Effect of constraint induced movement therapy on burned dominant hand function

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Effect of constraint induced movement therapy on burned dominant hand function

We investigate the Effect of constraint induced movement therapy on burned dominant hand function by using various measurement tools :

  • Hand grip strength by Hand held dynamometer
  • Metacarpophalangeal joint flexion (MCP) by goniometer
  • Function by michgan hand questionnaire A randomised controlled trial (2 groups) First group will receive constraint induced movement therapy (glove mitt) on sound hand .

Second group will receive the traditional treatment ( stretching - positioning ) We do the assessment before treatment and (4-8) after the start of treatment process.

Study Type

Interventional

Enrollment (Actual)

34

Phase

  • Not Applicable

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

  • Egypt
      • Giza, Egypt
        • Faculty of Physical Therapy Cairo University

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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age of patient 20 to 35
  • both male and female
  • suffer from dorsal hand dominant burn healed spontaneously or by graft
  • TBSA less than 20%
  • All patient active before injury.

Exclusion Criteria:

  • patient with fracture
  • patient with crush injuries
  • patient with contralateral hand burn
  • Patient with cardiovascular injury

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Sequential Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: group 1 received constraint induced movement therapy + traditional treatment
group 1 received constraint induced movement therapy + traditional treatment we will constraint affected hand and enforce patient to use affected side
Other: Constraint induced movement therapy
Constraint the sound side and encourage movement of the burned side
Other Names:
  • CIMT
Other: Positioning - stretching
Position hand in functional hand position - stretching against deformity position
Active Comparator: traditional treatment for hand burn positioning - RANGE OF MOTION
Other: Positioning - stretching
Position hand in functional hand position - stretching against deformity position

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hand grip strength
Time Frame: 8 weeks for each case
Strength measured by hand held dynamometer
8 weeks for each case
Metacarpophalangeal joint flexion
Time Frame: 8 weeks for each case
Range of motion by goinometer
8 weeks for each case
Hand function
Time Frame: 8 weeks for each case
By arabic version of michgan hand qurstionaire
8 weeks for each case

Collaborators and Investigators

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

Sponsor

Cairo 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)

May 22, 2024

Primary Completion (Actual)

August 1, 2024

Study Completion (Actual)

August 26, 2024

Study Registration Dates

First Submitted

November 25, 2024

First Submitted That Met QC Criteria

November 25, 2024

First Posted (Estimated)

November 27, 2024

Study Record Updates

Last Update Posted (Estimated)

November 27, 2024

Last Update Submitted That Met QC Criteria

November 25, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P.T.REC/012/005218

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

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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