- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06811766
Comparative Effects of Strain-counterstrain and Muscle Energy Techniques on Neck Pain and Functional Disability in Patients with Cervicogenic Headache (SCS METs)
January 31, 2025 updated by: Kinza Fatima, University of Faisalabad
The primary objective of this study is to compare effects of SCS and METs on reduction of neck pain intensity and improvement in functional disability in individuals with CGH.
The secondary objective is to assess the impact of both techniques on ROM in cervical spine
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
54
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 Contact
- Name: Kinza Fatima KFatima, MS physical therapy
- Phone Number: +92 495223727
- Email: drkinzagill@gmail.com
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:
- participants who fulfill the criteria of international headache society.
Exclusion Criteria:
- participants who have cervicogenic headache after cervical injury or head surgery.
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: 1
This group containing 27 participants
|
This is a technique that uses gentle body positioning passively to treat muscles and joints pain.
So, this can be effective for neck pain in patients with CGH
Other Names:
|
|
Active Comparator: 2
This group also containing 27 participants
|
This technique uses patient's own muscles to treat muscles and joint restrictions.
So, this technique can be prove affective for neck pain and limited range in patients with CGH
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual analogue scale
Time Frame: 3 weeks
|
To check pain intensity
|
3 weeks
|
|
Neck disability index
Time Frame: 3 weeks
|
To check functional disability
|
3 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Goniometer
Time Frame: 3 weeks
|
To measure range of motion
|
3 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 (Estimated)
February 1, 2025
Primary Completion (Estimated)
August 1, 2025
Study Completion (Estimated)
September 1, 2025
Study Registration Dates
First Submitted
January 31, 2025
First Submitted That Met QC Criteria
January 31, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 31, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TUFkinza
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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 Cervicogenic Headache
-
Des Moines UniversityCompleted
-
Meltem UzunCompletedExercise | Therapeutics | Headache, CervicogenicTurkey
-
Alabama Physical Therapy & AcupunctureUniversidad Rey Juan CarlosCompletedCervicogenic HeadachesUnited States
-
Hungarian University of Sports ScienceCairo UniversityCompleted
-
Istanbul Medipol University HospitalIstanbul Kent UniversityCompletedCervicogenic Headache | Cervicogenic HeadachesTurkey (Türkiye)
-
Foundation University IslamabadRecruiting
-
Cairo UniversityNot yet recruiting
-
University of LahoreCompletedCervicogenic HeadachePakistan
-
Hong Kong Baptist UniversityActive, not recruiting
-
MTI UniversityCompleted
Clinical Trials on Strain-counterstrain
-
Long Island UniversityTerminatedOther Instability, Ankle and FootUnited States
-
University Hospitals Cleveland Medical CenterWithdrawnChronic Migraine
-
Riphah International UniversityRecruitingTrigger Point Pain, MyofascialPakistan
-
Kyungnam UniversityCompletedLatent Myofascial Trigger Points | Upper Trapezius MuscleSouth Korea
-
Riphah International UniversityRecruiting
-
Loma Linda UniversityRecruitingLow Back Pain, Mechanical | Piriformis Syndrome | Somatic Dysfunction of Sacral Region (Finding)United States
-
Hasan Kalyoncu UniversityCompletedPain | Fibromyalgia | Physiotherapy | Strain Counterstrain TechniqueTurkey (Türkiye)
-
Cairo UniversityCompletedSacroiliac Joint Somatic DysfunctionEgypt
-
Cardenal Herrera UniversityCompleted
-
Universidad Católica San Antonio de MurciaCompletedLow Back Pain | Trigger Point Pain, MyofascialSpain