Effectiveness of Bowen Technique vs Muscle Energy Technique in Neck Pain.

July 3, 2025 updated by: Riphah International University

Effectiveness of Bowen Technique vs Muscle Energy Technique in Mechanical Neck Pain Among Desktop Users.

Mechanical neck pain, also known as non-specific neck pain, is a prevalent ailment that results from problems with spine and surrounding tissue function. Trauma, degenerative changes, strained muscles, and bad posture are among the causes. The range of symptoms includes headaches, stiffness, and mild to severe pain. The goal of treatment is to strengthen the muscles and improve posture. The diagnosis is clinical. The Bowen Technique is a type of gentle bodywork therapy that promotes relaxation and overall rebalancing by using specific movements to activate the autonomic nerve system. It is sought for the improvement of general well-being, pain alleviation, and stress reduction. Patients undergoing manual treatment will be asked to actively contract their muscles against regulated resistance using the Muscle Energy Technique (MET). It addresses problems including joint limitations and attempts to return muscles and joints to their normal functions.

Study Overview

Detailed Description

The research, will last for ten months at the Limit Institute of Health Sciences in Sahiwal, is a randomized controlled trial. With 10 participants in each group using a non-probability convenient sampling procedure, the sample size includes 10% attrition. Computer users between the ages of 18 and 35 who work five to seven hours a day meet the inclusion criteria, but recent musculoskeletal injuries and a history of head or spine trauma are the exclusion criteria. One instrument used to collect data is the Neck Disability Index (NDI). There are two established study groups: Group B will receive Muscle Energy Technique (MET) and traditional physiotherapy, while Group A will receive Bowen therapy and conventional physiotherapy. Blinding will be used, and the study will adhere to a recruitment, enrollment, and randomization procedure. SPSS version 23 will be used to analyze the data, and descriptive statistics, change over temporal analysis as well as tests of group comparison. The purpose of the study is to evaluate how the interventions affect people who use computers for extended periods in terms of their functional results and mechanical neck discomfort.

Study Type

Interventional

Enrollment (Actual)

36

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

    • Punjab
      • Sahiwal, Punjab, Pakistan, 57000
        • Maryam Polyclinic Sahiwal

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

  • Child
  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Computer users who work 5-7 hours daily.
  • Age between 18 to 35 will be included.
  • Both genders

Exclusion Criteria:

  • Any recent musculoskeletal injury of upper limb or spine.
  • History of any trauma of spine or head

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Bowen Therapy along with Conventional Therapy
Group A will receive Bowen Therapy along with Conventional Therapy

Bowen Technique Group Assignment: Participants will be assigned to undergo targeted Bowen Technique therapy sessions.

Session Details: The therapy sessions will include:

  • Gentle, rolling-type maneuvers
  • Specific placements of fingers and thumbs
  • Focus on muscles, tendons, and ligaments associated with neck pain Therapeutic Pauses: There will be intentional pauses between sets of moves to allow the body time to respond to the therapeutic stimulation.

Conventional Therapy: Hot pack, TENS, Passive Stretching 2 times a week for 4 weeks

Active Comparator: Muscle Energy Technique along with conventional Therapy
Group B will receive Muscle Energy Technique along with Conventional Therapy

MET Session Structure: Participants will engage in Muscle Energy Technique (MET) sessions that focus on:

  • Isometric muscle contractions, where muscles are contracted without changing length.
  • Therapist-guided, controlled contractions against specific resistance.
  • Relaxation Periods: Each contraction session will be followed by a period of relaxation to allow muscles to recover and respond to the therapy.

conventional therapy: Hot pack, TENS, Passive Stretching 2times a week for 4 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain level
Time Frame: 4th week
The Numeric Pain Rating Scale (NPRS) is a straightforward tool used to measure pain intensity in adults, including those suffering from chronic pain associated with rheumatic conditions. It features an 11-point scale, where '0' indicates no pain and '10' signifies the most extreme pain possible, described as "pain as bad as you can imagine" or "the worst pain imaginable."
4th week
Functional Disability
Time Frame: 4th week
A self-reported questionnaire called the Neck Disability Index (NDI) is used to gauge how neck pain affects a person's ability to function and go about their everyday life. It is divided into eleven sections that address different tasks such as sleeping, work, reading, lifting, and personal care. In each category, respondents rate the level of difficulty they encounter; scores are added together to produce a percentage that indicates the degree of disability. When conducting clinical assessments, the NDI is a useful instrument that helps medical practitioners determine the degree of functional limits and provide personalized interventions for patients with neck discomfort.
4th week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hafiza Wajeeha Saeed, DPT, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 15, 2024

Primary Completion (Actual)

May 15, 2025

Study Completion (Actual)

June 1, 2025

Study Registration Dates

First Submitted

June 11, 2024

First Submitted That Met QC Criteria

June 11, 2024

First Posted (Actual)

June 14, 2024

Study Record Updates

Last Update Posted (Actual)

July 4, 2025

Last Update Submitted That Met QC Criteria

July 3, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/RCR&AHS/23/01106

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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