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Clinical Trials/NCT04179214
NCT04179214
Completed
Not Applicable

Effects of Thoracic Spine Manipulation on Pressure Pain Sensitivity of Active Myofascial Trigger Points in Rhomboid Muscle

Riphah International University1 site in 1 country60 target enrollmentJuly 22, 2019
ConditionsTrigger Points

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Trigger Points
Sponsor
Riphah International University
Enrollment
60
Locations
1
Primary Endpoint
Numeric pain rating scale (NPRS)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study intends to determine the effects of thoracic manipulation on pressure pain sensitivity in patients with rhomboid active trigger points.

Detailed Description

This is a single blinded controlled trial and will be conducted at physiotherapy clinic of women institute of rehabilitation sciences Abbottabad. The "screw" manipulation is a fairly aggressive manipulative technique in which the transverse processes are forced into a posterior to anterior direction Individual will be screened out according to inclusion criteria. Individuals will be allocated randomly into two groups, 30 in thoracic manipulation group and 30 in conventional physiotherapy protocol group by sealed envelope method. Both groups will receive conventional physiotherapy protocol (manual pressure release technique and muscle imbalances exercises) for rhomboid trigger points in common and the experimental group will receive thoracic manipulation in addition to conventional protocol. Assessment will be done on baseline and after 3 weeks. Data will be analyzed on SPSS version 21.

Registry
clinicaltrials.gov
Start Date
July 22, 2019
End Date
December 30, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age between 18 to 30 years
  • Participants presented with interscapular pain
  • Forward head posture with active trigger points in rhomboid muscle
  • Segmental hypomobility in upper thoracic identified with positive springing test

Exclusion Criteria

  • Participants who demonstrated contraindication to manipulation
  • Open wounds or Trauma to the area which occurred less than two months prior treatment
  • Any neurological compromise
  • Mid scapular pain due to degenerative process or osteoporosis

Outcomes

Primary Outcomes

Numeric pain rating scale (NPRS)

Time Frame: post 3 weeks

Numeric pain rating scale (NPRS) is an 11 point (0-10) Scale used to measure pain. Patient verbally select value between (0-10) on the basis of intensity of pain. (0) means No pain and (10) means maximum pain experienced at baseline and after 3 weeks

Thoracic ROM

Time Frame: post 3 weeks

A thoraxic range of motion (TROM) inclinometer will be use to assess thoracic range of motion in flexion and extension.. Participants will be seated or standing upright and asked to actively move their trunk in forward and backward direction

Pain pressure threshold

Time Frame: post 3 weeks

It is measured with the help of an instrument called Algometer. The readings of Algometer are both in pounds and kilograms and it gauges the pressure at which patient feels pain.

Secondary Outcomes

  • Neck Disability Index (NDI)(post 3 weeks)

Study Sites (1)

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