Clinical and Electromyographic Effect of Tui Na Massage Versus Positional Release on Postpartum Neck Dysfunction

April 29, 2026 updated by: Kerolous Ishak Shehata, October 6 University

Clinical and Electromyographic Effect of Tui Na Massage Versus Positional Release on Postpartum Neck Dysfunction A Randomized Clinical Trial

To investigate the effects of Tui- Na massage versus Positional release technique on neck pain intensity, neck disability, and electromyographic characteristics of upper trapezius muscle.

Study Overview

Detailed Description

Positional release technique

Study Type

Interventional

Enrollment (Actual)

60

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

      • Cairo, Egypt
        • Kerolous ishak shehata kelini

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:

  • 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

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: 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

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)

December 20, 2025

Primary Completion (Actual)

March 25, 2026

Study Completion (Actual)

April 1, 2026

Study Registration Dates

First Submitted

November 22, 2025

First Submitted That Met QC Criteria

November 22, 2025

First Posted (Actual)

December 3, 2025

Study Record Updates

Last Update Posted (Actual)

May 1, 2026

Last Update Submitted That Met QC Criteria

April 29, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

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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