Effect of High Intensity Laser Versus Plus Exercises

September 12, 2021 updated by: hanaa mohsen, Badr University

Effectiveness of High Intensity Laser Therapy Plus Therapeutic Interventions in Treatment of Girls Gymnasts With Non-specific Wrist Pain

High-intensity laser therapy (HILT) has been used more recently in the therapeutic protocols of musculoskeletal pain management. This study is conducted to find out the effect of high intensity laser therapy only versus high intensity laser pulse exercises on level of wrist pain, function and Joint position sense in girls Gymnasts

Study Overview

Detailed Description

Effect of high intensity laser plus exercises on wrist pain ..three groups of gymnastics girls suffer from non specific wrist is allocating ..the first group will receive exercises only , the second will receive laser only while the third will receive exercises plus laser

Study Type

Interventional

Enrollment (Actual)

36

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

      • Cairo, Egypt
        • Hanaa Mohsen

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

10 years to 16 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • All girls diagnosed with generalized chronic wrist pain and referred by orthopaedic physician.
  • Their age between 10-16 years old
  • They will be able to follow instructions.
  • All are medically stable

Exclusion Criteria:

  • • Bone fractures and tumors.

    • Cases after plastic surgery.
    • Hypertension (due to secondary vasoconstriction)
    • Diabetes mellitus
    • Pacemakers

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
Other: Laser group
High Intensity Laser Therapy only , this group will receive laser for 4 weeks three times /week
high intensity laser only
Other: Exercise group
Exercise , selected physiotherapy exercises will receive for 4 weeks ,3times/week
exercise only
Other Names:
  • exercise only
Experimental: High intensity laser grouo
High intensity laser plus exercise will receive the selected exercises and laser 4 weeks, 3 times/week
high intensity laser plus exercise

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
PRWE
Time Frame: pre and post 4 weeks of intervention, decrease score indicate improvement
The PRWE is a 15-item questionnaire that is used to rate wrist outcomes based on patient pain and function and is based on an 11-point (0-10) scale.
pre and post 4 weeks of intervention, decrease score indicate improvement

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
JBS
Time Frame: pre and post 4 weeks of intervention, decrease score indicate improvement
JPS assesses precision or accuracy in repositioning a joint at a predetermined target angle
pre and post 4 weeks of intervention, decrease score indicate improvement

Collaborators and Investigators

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

Sponsor

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)

July 25, 2021

Primary Completion (Actual)

August 25, 2021

Study Completion (Actual)

August 30, 2021

Study Registration Dates

First Submitted

July 7, 2021

First Submitted That Met QC Criteria

July 20, 2021

First Posted (Actual)

July 30, 2021

Study Record Updates

Last Update Posted (Actual)

September 14, 2021

Last Update Submitted That Met QC Criteria

September 12, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • Hanaa 6

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

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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