- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07575139
Myofascial Release and Dynamic Cupping in Children
Comparative Effects of Myofascial Release Therapy and Dynamic Cupping on Neck Pain and Posture in School Going Children.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Neck pain is a highly prevalent musculoskeletal disorder that significantly impairs quality of life and restricts social, academic, and physical activities. Globally, neck pain is ranked as the fourth leading cause of disability, with an annual prevalence estimated between 30% and 50%. Chronic neck pain is defined as pain or discomfort experienced along the posterior cervical spine, extending from the superior nuchal line to the first thoracic spinous process, persisting for more than three months. In school-aged children, prolonged poor posture, excessive screen use, and heavy schoolbags contribute to the increasing incidence of neck pain and postural deviations, making early intervention essential.
This study is designed as a randomized clinical trial to evaluate and compare the effectiveness of myofascial release therapy and dynamic cupping therapy in reducing neck pain and correcting postural deviations in school-based children. The study will be conducted in selected schools, where data collection and treatment sessions will take place. Children aged 7 to 12 years, both boys and girls, who present with neck pain and observable postural deviations will be included in the study. Exclusion criteria will consist of children with skin infections, open wounds, or dermatological conditions in the neck or upper back region, neurological symptoms, recent use of analgesic medications, or reliance on assistive devices, to ensure participant safety and reduce confounding variables.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: IMRAN AMJAD, PhD
- Phone Number: 9233224390125
- Email: imran.amjad@riphah.edu.pk
Study Contact Backup
- Name: MUHAMMAD ASIF JAVEED, MS-PT
- Phone Number: 9233224209422
- Email: a.javeed@riphah.edu.pk
Study Locations
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-
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Lahore, Pakistan, 54000
- Recruiting
- Imran Amjad
-
Contact:
- MUHAMMAD ASIF JAVEED, MS-PT
- Phone Number: 923224209422
- Email: A.JAVEED@RIPHAH.EDU.PK
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children with age 13 to 16.
- Both boys and girls
- neck pain (NPRS score from 7 to 10)
- Presence of postural deviations (will be access by using Plumb line test)
Exclusion Criteria:
- Skin infections, open wounds, or dermatological conditions in the neck/upper back region
- Neurological symptoms (cerebral palsy, muscular dystrophy, multiple sclerosis)
- Recent use of analgesics
- use of assistive devices (collars)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Myofascial release therapy
The participants in this group will receive myofascial release therapy.
Stretching of neck muscles: hold of 15-30 seconds, repeat for 2 sets Isometric setting of neck muscle: (for 12 seconds, repeated for 2 sets, with 1- minute rest between sets) (neck flexion, neck extension, side flexion without changing their length or the angle of the joint, essentially holding a static position) Postural exercise for neck: (chin tucks) (shoulder elevation and drop) (shoulder retraction and protraction) (Cobra/Sphinx Pose) (hold for 5-10 sec, 2x set)
|
The participants in this group will receive myofascial release therapy.
Stretching of neck muscles: hold of 15-30 seconds, repeat for 2 sets Isometric setting of neck muscle: (for 12 seconds, repeated for 2 sets, with 1- minute rest between sets) (neck flexion, neck extension, side flexion without changing their length or the angle of the joint, essentially holding a static position) Postural exercise for neck: (chin tucks) (shoulder elevation and drop) (shoulder retraction and protraction) (Cobra/Sphinx Pose) (hold for 5-10 sec, 2x set)
|
|
Experimental: Dynamic cupping
The participants in this group will receive dynamic cupping. Stretching of neck muscles: hold of 15-30 seconds, repeat for 2 sets Isometric setting of neck muscle: (for 12 seconds, repeated for 2 sets, with 1- minute rest between sets) (neck flexion, neck extension, side flexion without changing their .length or the angle of the joint, essentially holding a static position) 3. Dynamic cupping: Dynamic cupping involves applying a silicone or plastic cup to lubricated skin and creating gentle suction by squeezing the cup 2-3 time. Once suction is established, the therapist glides the cup smoothly over the muscle fibers in slow, controlled stroke linear, circular, or fan-shape to mobilize soft tissue and fascia. The cup should move without causing excessive pulling or discomfort, typically for 2 minutes per area. The suction level is moderate to keep the cup attached while allowing movement |
Dynamic cupping involves applying a silicone or plastic cup to lubricated skin and creating gentle suction by squeezing the cup 2-3 time.
Once suction is established, the therapist glides the cup smoothly over the muscle fibers in slow, controlled stroke linear, circular, or fan-shape to mobilize soft tissue and fascia.
The cup should move without causing excessive pulling or discomfort, typically for 2 minutes per area.
The suction level is moderate to keep the cup attached while allowing movement, and the therapist continuously adjusts pressure based on feedback.
After treatment, the cup is gently lifted to release suction, and the skin is checked for any irritation
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
posture correction
Time Frame: 4th day
|
Posture correction refers to the improvement in head, neck, and shoulder alignment, particularly reduction in forward head posture and rounded shoulders.
It is measured using objective tools such as craniovertebral angle, postural assessment scales, or photographic analysis.
Improvement is indicated by increased alignment angles and a more neutral upright posture.
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4th day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
rang of motion
Time Frame: 4th day
|
Range of motion refers to the degree of movement available at the cervical spine in all directions, including flexion, extension, lateral flexion, and rotation.
It is measured using tools such as a goniometer or inclinometer to assess functional mobility.
Improvement is indicated by increased pain-free movement and greater cervical mobility in all planes.
|
4th day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: EAYZA RIAZ, MS-PT, RIPHAH INTERNATINAAL UNIVERSITY
Publications and helpful links
General Publications
- Guo Y, Lv X, Zhou Y, Li Z, She H, Bai L, Bao J. Myofascial release for the treatment of pain and dysfunction in patients with chronic mechanical neck pain: Systematic review and meta-analysis of randomised controlled trials. Clin Rehabil. 2023 Apr;37(4):478-493. doi: 10.1177/02692155221136108. Epub 2022 Oct 27.
- Mihcioglu EK, Guchan Topcu Z, Tunali AN, Mihcioglu S, Tomac H. Instrument-assisted soft tissue mobilization as a promising approach for children with chronic neck pain: A single-blind, randomized study. J Back Musculoskelet Rehabil. 2026 May;39(3):1044-1052. doi: 10.1177/10538127251401084. Epub 2025 Dec 7.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/EAYZARIAZ
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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