Impact of Resistance Training With and Without Venous Occlusion on Strength and Function Post (Hand Burn) (hand burn)

April 9, 2026 updated by: Hadeer Gamal Fouad Eltelemy, Cairo University

Impact of Resistance Training With and Without Venous Occlusion on Strength and Function Post Hand Burn

It will be hypothesized that There is There is no difference between resistance training with and without venous occlusion on hand strength and function post hand burn.

Study Overview

Detailed Description

The purpose of the study is to evaluate the difference between resistance training with and without venous occlusion on hand strength and function post hand burn.

This study will be designed to evaluate the difference between resistance training with and without venous occlusion on hand strength and function post hand burn.

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

    • Elmahalla Elkubra
      • Gharbia, Elmahalla Elkubra, Egypt, 3365

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
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Patients of all age groups and both sexes having less than sixty percent TBSA thermal burns and involves the hand.

    • Patients with second-degree (superficial or deep) burn on the hand.
    • Patients with third-degree burns
    • Patients with complete wound healing
    • Patients without any defects at tendons
    • Patients without burning at cubital fossa (cuff placement)
    • participants were required to have a resting (systolic and diastolic) blood pressure of <140/90 mmHg and a resting heart rate of <90 bpm
    • A decreased grip strength.
    • Patients without cognitive impairments and actively cooperating with treatment and measurements

Exclusion Criteria:

  • Any patient who has previous injury or congenital deformity of the hand with restricted hand function.
  • Resting systolic BP (BP) <140 mmHg and/or diastolic BP< 90 mmHg
  • Self-reported cardiovascular, metabolic, or pulmonary conditions or signs and symptoms suggestive of these diseases
  • Associated injuries affecting participation in exercise training, including fracture, amputation, acquired brain injury or peripheral neural injury or any pre-existing medical condition which may affect exercise participation.
  • patients that had fourth degree burns
  • patients that had first degree burns
  • Patients with burn at cubital fossa (cuff placement)
  • Patients without complete wound healing
  • patient who is taking medications that affect hemodynamic responses
  • Patients with severe hand burns leading to muscle and tendon damage, or those who have undergone finger amputation surgery
  • Patients who were not compliant for following up for at least once a month following discharge from hospital.

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: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: study group (aspirin Group)
Resistance exercises with venous occlusion This group will include 17 patients with hand burn who will receive treatment for burn which included: positioning, range of motion, stretch, joint mobilization and strength exercise for hand grip with blood flow restriction3 days per week for 4 weeks
patients with hand burn who will receive conventional treatment for burn which included: positioning, range of motion, stretch, joint mobilization and strength exercise for hand grip for 3 days per week for 4 weeks
Experimental: control
This group will include 17 patients with hand burn who will receive treatment for burn which included: positioning, range of motion, stretch, joint mobilization and strength exercise for hand grip with blood flow restriction3 days per week for 4 weeks
This group will include 17 patients with hand burn who will receive conventional treatment for burn which included: positioning, range of motion, stretch, joint mobilization and strength exercise for hand grip for 3 days per week for 4 weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
hand grip strength
Time Frame: twice first before beginning treatment from day 1 of treatment second after complete treatment after 1 month Assessment will be for 1 minute For assessment hand grip strength
Hand grip will be assessed by digital Hand Dynamometer
twice first before beginning treatment from day 1 of treatment second after complete treatment after 1 month Assessment will be for 1 minute For assessment hand grip strength

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
upper limb function
Time Frame: twice first pre treatment at 1 day for almost 5 minutes to assess all functions of upper limb function second after complete treatment after 1 month to assess upper limb function after treatment for 5 minutes
Function of hand will be assessed by quick disabilities of arm, shoulder and hand questionnaire which asks patient about symptoms as well as ability to perform certain activities This scale which which assess upper limb function and high score means high disability and bad results and low score means low disability and good results
twice first pre treatment at 1 day for almost 5 minutes to assess all functions of upper limb function second after complete treatment after 1 month to assess upper limb function after treatment for 5 minutes

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

November 20, 2025

Primary Completion (Actual)

January 1, 2026

Study Completion (Actual)

January 30, 2026

Study Registration Dates

First Submitted

November 13, 2025

First Submitted That Met QC Criteria

November 13, 2025

First Posted (Actual)

November 14, 2025

Study Record Updates

Last Update Posted (Actual)

April 14, 2026

Last Update Submitted That Met QC Criteria

April 9, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • P.T.REC/012/006079

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

it is considered privacy of patients and privacy of my research

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.

Clinical Trials on Hand Burn

Clinical Trials on resistance exercise with venous occlusion

Subscribe