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Clinical Trials/CTRI/2024/03/064347
CTRI/2024/03/064347CompletedPhase 1

Efficacy of Muscle Energy Technique with stretching versus Muscle Energy Technique with myofascial release in upper cross syndrome

Guru Jambheshwar University of Science and Technology1 site in 1 country44 target enrollmentStarted: April 1, 2024Last updated:

Trial Snapshot

Phase
Phase 1
Status
Completed
Sponsor
Enrollment
44
Locations
1
Primary Endpoint
craniovertebral angle

Study Overview

Brief Summary

A comparative study on population with upper cross syndrome. Cervical pain is the most common musculoskeletal disorder which further leads to secondary complications if left untreated. Secondary complications further include upper cross syndrome. This condition most commonly affects persons with sedentary lifestyles, computer users, and people who sit in slouch positions for long periods. The prevalence of upper cross syndrome in the general population is 15 – 44% per year whereas in office workers prevalence is up to 50 to 60 %. The prevalence of upper cross syndrome among college-going students is around 48.7%. management of this condition includes manual therapy that includes stretching, strengthening, muscle energy technique, myofascial release, and postural corrective exercises. Subjects will be screened for upper cross syndrome using inclusion criteria. Informed consent will be taken for participation in the study. Participants will be allocated in two groups. Treatment protocol for group A – hot packs (10-15 minutes); muscle energy technique (4 repetitions with stretch hold for 8-10 seconds); stretching(4 repetitions stretch hold for 20 seconds). Treatment protocol for group B- hot packs (10-15 minutes); muscle energy technique(4 repetitions with stretch hold for 8-10 seconds); myofascial release( given to trigger points with the help of knuckles, fingers, or elbow). Treatment will be given for 3 weeks on alternate days. Data would be recorded 4 times including at day 0, at the end of the 1st week, at the end of the 2nd week, and at the end of the 3rd week.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
17.00 Year(s) to 30.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Neck pain
  • Consent to participate in the study.

Exclusion Criteria

  • Any neurological disorder
  • Any cardiovascular disorder
  • Any surgical history of neck
  • Uncooperative patients
  • People older than 30 years of age 6.

Outcomes

Primary Outcomes

craniovertebral angle

Time Frame: The outcomes will be assessed for 4 times at the baseline, after 1 week of treatment, after 2 weeks of treatment and after 3 weeks of treatment

Secondary Outcomes

  • cervical range of motion(The outcomes will be assessed for 4 times at the baseline, after 1 week of treatment, after 2 week of treatment and after 3 week of treatment)

Investigators

Sponsor
Guru Jambheshwar University of Science and Technology
Sponsor Class
Other [government University]
Responsible Party
Principal Investigator
Principal Investigator

Ravita Phogat

Guru Jambheshwar University of Science and Technology

Study Sites (1)

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