- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07261605
Clinical and Electromyographic Effect of Tui Na Massage Versus Positional Release on Postpartum Neck Dysfunction
Clinical and Electromyographic Effect of Tui Na Massage Versus Positional Release on Postpartum Neck Dysfunction A Randomized Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Cairo, Egypt
- Kerolous ishak shehata kelini
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- age ranged from 20- 40 years
- had post partum cervical pain
- score above 15 in the neck disability index (NDI
Exclusion Criteria:
- Patients with structural, inflammatory, infectious, metabolic, congenital, traumatic spinal disorders and spinal or upper limb surgery.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: postural correction
20 patients: will receive postural correction exercises program only.
|
A combination of yoga, stretching, and strengthening exercises may help you to fix or correct your posture over time. Maintaining good posture is important for helping you develop strength, flexibility, and balance. |
|
Experimental: Tui NA massage
20 patients: will receive postural correction exercises program.
In addition, an experienced therapist will apply the Tui Na massage to the cervical region
|
Tuina massage is similar to acupuncture in that it targets specific acupoints, but practitioners use fingers instead of needles to apply pressure to stimulate these points.
Tuina massage is often used in combination with acupuncture.
|
|
Experimental: Positional release
20 patients: will receive postural correction exercises program.
In addition, the therapist put the patient in a comfortable posture for ninety seconds, after which they passively will be moved back to their initial positions
|
is a passive manual manipulation method used to alleviate musculoskeletal pain and dysfunction.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Electromyography
Time Frame: 4 weeks
|
used for measuring upper trapezius normalized Root mean square to indicate muscular activities and median frequence to indicate muscular fatigue.
Active electrode will be located 2 cm lateral to the midpoint of a line drawn between C7 spinous process and the posterolateral acromion while the reference one will be located over the C7 spinous process.
|
4 weeks
|
|
visual analogue scale
Time Frame: 4 week
|
10 cm horizontal line anchored by and it is a line score from zero to ten which 10 score means it is the worse of pain and zero score means the least pain ""no pain"" on the leftand ""worst imaginable pain"" on the right).
Patients indicate their pain intensity by marking on the point at the line that reflect their pain
|
4 week
|
|
Neck disability index
Time Frame: 4 weeks
|
It includes 10 questions of which 7 examine functional activities, 2 ask about symptoms and a question considers concentration. Each Patient will circle one of the six options describing the severity of each item (0 5). total score for the questionnaire out of 50. Higher scores represent greater disability. |
4 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- PT.BU.EC.20
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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