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Clinical Trials/NCT07331571
NCT07331571
Completed
Not Applicable

Effects of Myofascial Release With and Without Autogenic Inhibition Muscle Energy Technique in Patients With Non-specific Chronic Neck Pain

Riphah International University1 site in 1 country44 target enrollmentStarted: January 13, 2025Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
44
Locations
1
Primary Endpoint
Numeric Pain Rating Scale

Overview

Brief Summary

The study was conducted to determine the effects of myofascial release therapy with and without autogenic inhibition muscle energy technique in patients with non-specific chronic neck pain.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Neck pain for at least 3 months
  • Pain intensity on NPRS between 4 to 7
  • Limited neck range of motion
  • Use of computer for at least 2 hours daily
  • Negative Sharp-Purser and alar ligaments test (to rule out atlantoaxial instability, integrity of transverse and alar ligaments)

Exclusion Criteria

  • History of trauma
  • Cervical spine fracture
  • Open neck surgery
  • Cervical radiculopathy
  • Paresthesia
  • Cervical myelopathy
  • Rheumatoid Arthritis
  • Ankylosing Spondylitis
  • Multiple Sclerosis
  • Fibromyalgia

Arms & Interventions

Myofascial Release Therapy

Active Comparator

Intervention: Myofasical Release Therapy (Other)

Myofascial Release Therapy

Active Comparator

Intervention: Standardized Physiotherapy Treatment (Other)

Myofascial Release with Autogenic Inhibition Muscle Energy Technique

Experimental

Intervention: Autogenic Inhibition Muscle Energy Technique (Other)

Myofascial Release with Autogenic Inhibition Muscle Energy Technique

Experimental

Intervention: Myofasical Release Therapy (Other)

Myofascial Release with Autogenic Inhibition Muscle Energy Technique

Experimental

Intervention: Standardized Physiotherapy Treatment (Other)

Outcomes

Primary Outcomes

Numeric Pain Rating Scale

Time Frame: From enrollment to the end of treatment at 6 weeks

Numeric Pain Rating Scale is utilized to evaluate pain. It consists of 11 points, having an overall score ranging from 0 and 10, where: 0 represents no pain, 1 - 3 represents mild pain, 4 - 6 represents moderate pain and 7 - 10 represents the most severe pain.

Neck Disability Index

Time Frame: From enrollment to the end of treatment at 6 weeks

Neck Disability Index is a questionnaire that has 10-questions for determining cervical pain and functional disability linked with the activities of daily living. It consists of questions on pain intensity, personal care, lifting, reading, headaches, concentration, work, driving, sleeping and recreation. Scores in each item is described in 6 stages, from 0 to 5 points. The total of 0-4 points indicate no disability, 5-14 points indicate mild disability, 15-24 points indicate moderate disability, 25-34 points indicate severe disability and 35-50 points indicate complete disability

Secondary Outcomes

  • ROM Cervical Spine (Rotation) Left Side(From enrollment to the end of treatment at 6 weeks)
  • ROM Cervical Spine (Lateral Flexion) Left Side(From enrollment to the end of treatment at 6 weeks)
  • ROM Cervical Spine (Flexion)(From enrollment to the end of treatment at 6 weeks)
  • ROM Cervical Spine (Extension)(From enrollment to the end of treatment at 6 weeks)
  • ROM Cervical Spine (Rotation) Right(From enrollment to the end of treatment at 6 weeks)
  • ROM Cervical Spine (Lateral Flexion) Right Side(From enrollment to the end of treatment at 6 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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