Skip to main content
Clinical Trials/CTRI/2025/09/094489
CTRI/2025/09/094489Not yet recruitingNot Applicable

Effectiveness of Muscle Energy Technique and Blackburn Exercises on Pain, range of motion and Postural dysfunction in IT Professionals with Upper Cross Syndrome- A Comparative Study

Not provided1 site in 1 country60 target enrollmentStarted: December 6, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
60
Locations
1
Primary Endpoint
VAS score readings will be taken pre-and post-intervention.

Study Overview

Brief Summary

This study is Randamized, parallel group, active-controlled trial, finding the effect of MET and Blackburn exercises on the pain, range of motion, and postural dysfunction in IT professionals suffering from Upper Cross Syndrome. Subjects will undergo testing using ROM, MMT, VAS, NDI, and various tests assessing tight musculature and weak musculature, with pre-treatment scores being recorded.Both groups will receive an intensive treatment schedule for 1 hour/day, 3 days/week, for 6 consecutive weeks, along with the routine daily activity. The subjects performed the conventional exercise daily and recorded their progress in a home exercise log. After 6 weeks of treatment procedures all the subjects will undergo re-evaluation by MMT, ROM, Special test, VAS, and NDI to obtain specific differences in their motor function and quality of life, and the readings will be subjected to statistical analysis.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
None

Eligibility Criteria

Ages
30.00 Year(s) to 40.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Diagnosed with upper cross syndrome by taking an assessment Subjects willing to participate in the study Not participating in any formal physical rehabilitation program.

Exclusion Criteria

  • Surgeries to the cervical area Subjects taking analgesics and/or muscle relaxants.
  • Known thoracic scoliosis, VBI, and kyphosis Known rotator cuff tear Pregnancy Cervical Radiculopathy Ankylosing spondylitis Inflammatory arthritis Herniation or stenosis The patient is not willing to participate in the study.

Outcomes

Primary Outcomes

VAS score readings will be taken pre-and post-intervention.

Time Frame: VAS score is a universally accepted, valid and reliable tool to measure pain with a 10 grading, mild (0-3), moderate (4-6), and severe (7-9).

Secondary Outcomes

  • NECK DISABILITY INDEX(NECK DISABILITY INDEX)

Investigators

Sponsor
Not provided
Responsible Party
Principal Investigator
Principal Investigator

vandana vyas

Shama Institute of Medical Sciences

Study Sites (1)

Loading locations...

Similar Trials

Comparative Study on the Effectiveness of... | Clinical Trial