Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
Actively Recruiting
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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