Actively Recruiting

Phase Not Applicable
Age: 35Years - 55Years
All Genders
ID07628348

Effects of Diaphragmatic Release Technique on Neck Pain, Range of Motion, and Chest Expansion in Patients With Cervical Radiculopathy

Led by Riphah International University · Updated on 2026-06-05

40

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of the diaphragmatic release technique on neck pain, cervical range of motion, and chest expansion in patients with cervical radiculopathy. This randomized controlled trial aims to compare this technique combined with standard treatments against traditional physical therapy. The study addresses the gap in research on the impact of respiratory dysfunction in cervical radiculopathy treatment and explores how diaphragm function relates to neck pain and disability. Participants will be randomly assigned to one of two groups for a four-week treatment period. The experimental group will receive the diaphragmatic release technique for 5 minutes along with cervical distraction, cervical isometrics, and neurodynamic mobilization of the median and ulnar nerves. The control group will receive traditional physical therapy including cervical distraction, isometrics, and neurodynamic mobilization without the diaphragmatic release. Each session lasts approximately 40 minutes and occurs three times per week for four weeks. During the study, participants will be assessed at the fourth week for neck pain intensity using the Numeric Pain Rating Scale, cervical spine range of motion in flexion, extension, lateral flexion, and rotation using an inclinometer, and chest expansion measured with a tape. These evaluations help measure the impact of the treatments on pain, movement, and respiratory function. The study begins in January 2026 and continues until August 2026, with participants aged 35 to 55 years involved in the trial.

CONDITIONS

Brief Title

Effects of DRT on Neck Pain, ROM, and Chest Expansion in Patients With CR

Who Can Participate

Age: 35Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Presence of unilateral neck pain and paresthesia symptoms for about 2 months
  • Presence of posterolateral disc herniation at the C4-C7 level
  • A positive spurling test
  • Positive upper limb neural tension tests for the median and ulnar nerve
  • Cervical rotation towards the painful side of less than 60 degrees
  • Chest Expansion of less than 4 cm
  • Age between 35 and 55 years
  • Any gender
Not Eligible

You will not qualify if you...

  • Any tumor
  • Fracture
  • Osteoporosis
  • Scoliosis
  • Cervical and shoulder instability
  • Diabetic neuropathy
  • History or presence of a respiratory disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants receive diaphragmatic release technique or traditional physical therapy including cervical distraction, cervical isometrics, and neurodynamic mobilization over four weeks.

3 visits per week for 4 weeks

Trial Site Locations

Total: 1 location

1

Iffat Anwar Medical Complex

Lahore, Punjab Province, Pakistan, 54600

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Research Team

I

Imran Amjad, phd

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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