- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05939583
Effect of Shock Wave Therapy on Upper Trapezius Trigger Points in Patients With Cervicogenic Headache.
March 12, 2024 updated by: Ahmed Magdy Alshimy, October 6 University
Effect of Shock Wave Therapy on Upper Trapezius Trigger Points in Patients With Cervicogenic Headache. a Randomized Controlled Trial
Control group will receive US, TENS, IR and exercises.
The treatment group will receive the same program in addition to shock waves therapy.
Patients will receive 3 sessions per week for 4 weeks.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Control group will receive US, TENS, IR and exercises.
The treatment group will receive the same program in addition to shock waves therapy.
Patients will receive 3 sessions per week for 4 weeks.
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
-
-
Giza
-
El-Sheikh Zayed City, Giza, Egypt, 1133
- October 6 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:
- Fifty patients from both genders.
- Age ranging from 20 to 40 years.
- Referred by an orthopedist with a diagnosis of Mechanical neck dysfunction (MND) to physical therapy at the outpatient clinic of the Faculty of Physical Therapy, MTI University.
Exclusion Criteria:
- All other disorders.
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: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment Group
The treatment group will receive US, TENS, IR and exercises in addition to shock waves therapy.
Patients will receive 3 sessions per week for 4 weeks
|
Receiving Shock wave therapy + US, TENS, IR and exercises.
Other Names:
Receiving US, TENS, IR and exercises only.
|
|
Experimental: Control Group
Control group will receive US, TENS, IR and exercises.
Patients will receive 3 sessions per week for 4 weeks
|
Receiving US, TENS, IR and exercises only.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neck disability index
Time Frame: 4 weeks
|
Assess degree of neck disability.
|
4 weeks
|
|
Visual analogue scale
Time Frame: 4 weeks
|
Assess degree of pain from 1 (No Pain) to 10 (Severe Pain)
|
4 weeks
|
|
Kinesiological EMG
Time Frame: 4 weeks
|
Analysis of root mean square for upper trapezius muscle functions.
|
4 weeks
|
|
Kinesiological EMG
Time Frame: 4 weeks
|
Analysis of median frequency for upper trapezius muscle functions.
|
4 weeks
|
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)
February 1, 2022
Primary Completion (Actual)
September 1, 2022
Study Completion (Actual)
February 1, 2023
Study Registration Dates
First Submitted
July 3, 2023
First Submitted That Met QC Criteria
July 3, 2023
First Posted (Actual)
July 11, 2023
Study Record Updates
Last Update Posted (Actual)
March 15, 2024
Last Update Submitted That Met QC Criteria
March 12, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/2111/MTI.PT/2303123
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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