Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
NCT07026006

Active Release Versus Strain-Counter-strain Technique in Patients With Non-Specific Neck Pain

Led by Riphah International University · Updated on 2025-06-18

40

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study design will be a randomized clinical trial (RCT) aims to compare the effects of Active Release Technique and Strain-Counterstrain on pain, range of motion, cranio-vertebral angle, and disability in patients with non-specific neck pain. Data will be collected from Safi Teaching Hospital, Faisalabad, Pakistan. Using a non-probability purposive sampling method, participants aged 18-45 years with localized cervical pain and stiffness will be selected based on inclusion and exclusion criteria. The inclusion and exclusion criteria will be; Participants aged 18-45, both male and female, experiencing neck pain for at least 2 months, with palpable taut bands in upper trapezius and SCM, active trigger points in upper trapezius, levator scapulae, and SCM, NPRS score \>3/10 for neck region, and localized pain/stiffness in cervical spine (C3-C7) without upper limb radiculopathy, confirmed by negative Spurling's test, upper limb tension test, and shoulder abduction test. Subjects will be excluded if presented with a history of Participants who received myofascial treatment in the preceding month or have a diagnosis of fibromyalgia, KNGF Clinical Practice Guideline Grade III or IV, or neurological deficits. Participants will be equally divided into 2 groups using a random number generator table. Group A will receive Active Release Technique, while Group B will receive Strain-Counterstrain. Both groups will also receive hot packs, superficial neck muscles stretching, and neck isometrics. Outcome measures, including the Numerical Pain Rating Scale for pain, goniometer for range of motion, cranio-vertebral angle measurement, Neck Disability Index, will be assessed at baseline and after four weeks. Ethical approval will be obtained from the Ethical Committee of Riphah International University, and informed consent will be secured from all participants. The outcomes will focus on pain intensity, cervical range of motion, cranio-vertebral angle, and disability, Data analysis will be performed using SPSS version 25. The findings are expected to provide valuable insights into the comparative efficacy of these manual therapy techniques, informing clinical practice and improving patient outcomes in the management of non-specific neck pain.

CONDITIONS

Official Title

Active Release Versus Strain-Counter-strain Technique in Patients With Non-Specific Neck Pain

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 45 years
  • Male or female
  • Neck pain lasting at least 2 months
  • Palpable taut bands in upper trapezius and sternocleidomastoid muscles
  • Active trigger points in upper trapezius, levator scapulae, and sternocleidomastoid muscles
  • Neck pain score greater than 3 out of 10 on the Numerical Pain Rating Scale
  • Craniovertebral angle less than 53 degrees
  • Grade 2 severity of neck pain according to KNGF Guidelines
  • Localized neck pain or stiffness in cervical spine (C3-C7) without upper limb radiculopathy
  • Negative results on Spurling's test, upper limb tension test, and shoulder abduction test
Not Eligible

You will not qualify if you...

  • Received myofascial treatment in the past month
  • Diagnosis of fibromyalgia
  • Congenital problems
  • Received trigger point injections
  • Grade III or IV severity of neck pain according to KNGF Guidelines
  • Respiratory or joint disease
  • Neurological deficits

AI-Screening

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Trial Site Locations

Total: 1 location

1

Riphah Rehabilitation Clinic

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

S

Syed Shakil ur Rehman, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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