- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05120089
Muscle Energy Technique Versus Myofacial Release in Adolescents With Spinal Deformity
March 15, 2023 updated by: Amira Hussin Hussin Mohammed, Delta University for Science and Technology
Spinal deformity may not only alter the physical appearance, but may also have a psychological impact on the child, particularly in the adolescent to whom self- image is so important.
This study will investigate the effect of muscle energy technique compared to myofacial release in the adolescent with spinal deformities( scoliosis and/ or kyphosis).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
50
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
- AAA
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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
12 years to 16 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Children in this group will be healthy category according to CDC (Centers for Disease Control and Prevention) growth chart which ranged from BMI-for-age 5th to 85th percentiles . All children are normal &perform all activities of daily living
- They were able to understand and follow verbal commands and instructions included in the testing procedures.
Exclusion Criteria:
- All of them could be part of recreational activities in their public schools but no competitive sports. Children who participated in any regular sport activities involving the lower extremities will be excluded.
- None of them had any surgical intervention .
- None of them had any history of other musculoskeletal deformities or neuromuscular disorders.
- hey had neither visual, auditory defect.
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 |
|---|---|
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Experimental: muscle energy technique
Muscle energy technique is an associate degree of osteopathic manipulation methodology.
The muscles of patients were used, on request, to type a singular controlled position, in a very specific direction, and against a distinctly executed therapist-applied counterforce.
Muscle energy technique could be a post-isometric relaxation, because it reduces the tone of a muscle or cluster of muscle after a brief period following an isometric contraction.
The result of post-isometric relaxation is mediated by receptive input from Golgi connective tissue organ (GTO) that has associate degree repressive result on the antagonist muscles mediated by the muscle spindle receptive.
The technique will be applied for three month (3 session/week)
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Each technique will be applied for three month (3 session/week)
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Experimental: myofacial release
The technique will be applied for three month (3 session/week).
All participants underwent ipsilateral side bending in a side-lying position, with the goals being de-rotation and scoliosis reduction.
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Each technique will be applied for three month (3 session/week)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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cobb angle for spinal deformities (scoliosis and/or kyphosis)
Time Frame: immediately before the beginning of the intervention procedures
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It is defined as the greatest angle at a particular region of the vertebral column, when measured from the superior endplate of a superior vertebra to the inferior endplate of an inferior vertebra.
However, the endplates are generally parallel for each vertebra, so not all sources include usage of a superior versus inferior endplate in the definition.
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immediately before the beginning of the intervention procedures
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cobb angle for spinal deformities (scoliosis and/or kyphosis)
Time Frame: by the end of successful three month of intervention
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It is defined as the greatest angle at a particular region of the vertebral column, when measured from the superior endplate of a superior vertebra to the inferior endplate of an inferior vertebra.
However, the endplates are generally parallel for each vertebra, so not all sources include usage of a superior versus inferior endplate in the definition.
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by the end of successful three month of intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 17, 2021
Primary Completion (Actual)
January 31, 2023
Study Completion (Actual)
January 31, 2023
Study Registration Dates
First Submitted
September 17, 2021
First Submitted That Met QC Criteria
November 4, 2021
First Posted (Actual)
November 15, 2021
Study Record Updates
Last Update Posted (Actual)
March 17, 2023
Last Update Submitted That Met QC Criteria
March 15, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- muscle energy technique
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Time Frame
after publishing by 12 month
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
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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