Effect of Muscle Energy Technique on Craniovertebral and Shoulder Angles in Forward Head Posture

March 26, 2026 updated by: Heba saeid Mohamed Ahmed Elfaky, Cairo University
The study will be determine how muscle energy strategy for the upper trapezius and sternocleidomastoid muscles affects the craniovertebral angle and shoulder angle.

Study Overview

Detailed Description

Participants in group (A) received PIR for upper trapezius and sternocleidomastoid muscles. the therapist moved the subject's head into the position that put each muscle in stretch, once resistance/ barrier was felt, that position was held and subjects were asked to isometrically contract the target muscle with 20% of maximal contraction for 5 sec against mild resistance from the therapist, relax for 5 sec followed by passive stretch until reaching a new barrier for 30 sec, 3 repetitions for each muscle, 3sessions /week over a period of 4 weeks . In addition to the program designed for control group.

The treatment protocol was designed based on the assumption that the targeted muscles are the most shortened muscles in FHP.

PIR for upper trapezius The patient sat on a stool in an erect position. The therapist stood behind the patient with one hand on the patient's ipsilateral shoulder for stabilization, while the other was on the side of the patient's head. The patient's head was moved to flexion, lateral bending to the opposite side and rotation to the same side of the stretched muscle. The ipsilateral hand pushed the shoulder inferiorly to lengthen the muscle until the restrictive barrier was met, then we asked the patients to raise the shoulder against the hand isometrically then gently stretch the muscle until meeting a new barrier.

PIR for upper trapezius PIR for Sternocleidomastoid The patient sat on a stool in an erect position. The therapist stood behind the patient with her forearm on the patient's ipsilateral shoulder for stabilization, while the hands surrounded the patient's head. The head moved into lateral flexion away from the side of the involvement, rotation to the side of involvement, extension of the lower cervical spine and flexion of upper cervical spine to meet the restrictive barrier. The patient was instructed to push forward against the therapist's hand isometrically, and then gently stretch the muscle until meeting a new barrier.

Group (B) Participants in group (B) received static stretching exercise for upper trapezius and sternocleidomastoid .

Repetitions: 3times/day, 3days/week over a period of 4 weeks, in addition to strengthening exercises of deep cervical flexors and scapular retractor muscles, 3sets of 12 repetitions with 6 sec hold. In addition to postural advices Strengthening of deep cervical flexor muscles Each participant was instructed to sit with his arms relaxed at the side. The area above the lip and under the nose was lightly touched and the patient was asked to tuck his head down and in. The correct movement of tucking the chin in and straightening the spine were verbally reinforced. From sitting position, the patient was asked to tuck chin so that ears were in line with the tip of shoulders.

Strengthening of the scapular retractor muscles The participant sat on a chair without back support. The movement of the medial border of the scapula was gently resisted and the subject pinch them together "retraction". The subject was asked to imagine "holding a quarter between both the shoulder blades". Instructing each subject not to extend the shoulders or elevate the scapulae. The participant then stranded with his hands grasped together behind the lower back (this activity cause scapular adduction). The patient is instructed to adduct scapula and to hold the adducted position with both arms lowered downwards.

Postural education

• Postural advice They were advised that they should not sleep on a foam rubber pillow; should use a chair with proper back support and an arm rest of an appropriate height to provide elbow support while working at a keyboard and computer; should avoid leaning forward toward the screen of a computer or on a desk while writing for a prolonged period; and should avoid prolonged conversation on a telephone while holding the receiver by tilting the neck. Furthermore, the participants were advised to relieve muscle tension after every 20-30 minutes of work by getting up; stretching the arm, shoulder, neck, and back muscles; and walking to turn off the buzzer and reset the timer. They should either avoid prolonged carrying of a bag on any one side of the shoulder or balance the hanging weight of the bag on both sides of the shoulder.

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

      • Giza, Egypt
        • Cairo University

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

18 years to 23 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Both sex will be included with age ranged between (18-23) years old
  • subject with CVA less than 50°
  • subject with shoulder angle less than 52.28°.
  • Subjects without neck or shoulder pain or recent shoulder fracture.
  • Body mass index between (18-31) Kg/m2
  • They will understand and follow instructions included in the test.

Exclusion Criteria:

  • Neck pain
  • Shoulder pain
  • Recent shoulder fracture
  • Athlete
  • Cervical disc
  • Radiculopathy
  • Subjects had symptoms of vertigo, dizziness.
  • Subjects had visual or auditory problems.
  • Subjects had an autoimmune disease or systemic disease

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: treatment group
(30) thirty patients with forward head received PIR for upper trapezius and sternocleidomastoid muscles. the therapist moved the subject's head into the position that put each muscle in stretch, once resistance/ barrier was felt, that position was held and subjects were asked to isometrically contract the target muscle with 20% of maximal contraction for 5 sec against mild resistance from the therapist, relax for 5 sec followed by passive stretch until reaching a new barrier for 30 sec, 3 repetitions for each muscle, 3sessions /week over a period of 4 weeks In addition to the program designed for control group.
Post isometric relaxation for upper trapezius and sternocleidomastoid muscles. the therapist moved the subject's head into the position that put each muscle in stretch, once resistance/ barrier was felt, that position was held and subjects were asked to isometrically contract the target muscle with 20% of maximal contraction for 5 sec against mild resistance from the therapist, relax for 5 sec followed by passive stretch until reaching a new barrier for 30 sec, 3 repetitions for each muscle, 3sessions /week over a period of 4 weeks, In addition to the program designed for control group
Other Names:
  • post isometricrelaxation for upper trapezius and sternocleidomastoid muscles
static stretching exercise for upper trapezius and sternocleidomastoid . Repetitions: 3times/day, 3days/week over a period of 4 weeks, in addition to strengthening exercises of deep cervical flexors and scapular retractor muscles, 3sets of 12 repetitions with 6 sec hold. In addition to postural advices
Other Names:
  • traditional tretment
Sham Comparator: control group

(30) thirty patients with forward head received static stretching exercise for upper trapezius and sternocleidomastoid .

Repetitions: 3times/day, 3days/week over a period of 4 weeks, in addition to strengthening exercises of deep cervical flexors and scapular retractor muscles 3sets of 12 repetitions with 6 sec hold. In addition to postural advices

static stretching exercise for upper trapezius and sternocleidomastoid . Repetitions: 3times/day, 3days/week over a period of 4 weeks, in addition to strengthening exercises of deep cervical flexors and scapular retractor muscles, 3sets of 12 repetitions with 6 sec hold. In addition to postural advices
Other Names:
  • traditional tretment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
craniovertebral angle
Time Frame: one month
(CVA): It is the angle formed between a horizontal line through the spinous process of C7 and a line from the tragus of the ear It is a measure of forward head posture
one month
shoulder angle
Time Frame: one month
(SA) : is formed at a line between the center of the humerus and spinous process of C7 and the horizontal line through the center of the humerus. It is a measure of rounded shoulder posture.
one month
Pressure Pain Threshold
Time Frame: one month
the point at which a non-painful pressure stimulus turns into a painful pressure sensation Subjects' pressure pain thresholds (PPTs) were assessed using a Commander algometer
one month

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Heba Elfaki, MSc, Assist. lecture faculty of physical therapy Cairo 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.

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)

March 22, 2021

Primary Completion (Actual)

November 3, 2022

Study Completion (Actual)

January 8, 2023

Study Registration Dates

First Submitted

November 9, 2022

First Submitted That Met QC Criteria

December 6, 2022

First Posted (Actual)

December 8, 2022

Study Record Updates

Last Update Posted (Actual)

March 31, 2026

Last Update Submitted That Met QC Criteria

March 26, 2026

Last Verified

November 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • P.T.REC/012/003845

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.

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