- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04984187
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
Status
Completed
Intervention / Treatment
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
-
-
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Cairo, Egypt
- Hanaa Mohsen
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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
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exercise only
Other Names:
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Experimental: High intensity laser grouo
High intensity laser plus exercise will receive the selected exercises and laser 4 weeks, 3 times/week
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high intensity laser plus exercise
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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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