NCT07724470 Effects of Myokinetic Stretching Technique and Post Facilitation Stretching on Pain, Range of Motion, and Functional Disability in Patients With Cervical Radicular Pain
| NCT ID | NCT07724470 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Lahore University of Biological and Applied Sciences |
| Condition | Cervical Radicular Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 40 participants |
| Start Date | 2026-06-29 |
| Primary Completion | 2026-07-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 40 participants in total. It began in 2026-06-29 with a primary completion date of 2026-07-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Cervical radicular pain (CRP) is a musculoskeletal condition characterized by neck pain radiating to the upper limb due to compression or irritation of cervical nerve roots. It significantly affects daily activities, cervical mobility, and overall quality of life. Conventional physical therapy focuses on reducing pain and improving function; however, there is limited evidence comparing the effectiveness of different stretching techniques used in clinical practice. This randomized controlled trial aims to compare the effectiveness of Myokinetic Stretching Technique (MST) and Post Facilitation Stretching (PFS) on pain intensity, cervical range of motion, and functional disability in patients with cervical radicular pain. A total of 70 participants with cervical radicular pain (\>4 weeks) will be randomly allocated into two groups: Group A (Myokinetic Stretching Technique Group) - receiving MST along with conventional therapy including hot pack application, cervical isometric exercises, neurodynamic gliding, and continuous cervical traction. Group B (Post Facilitation Stretching Group) - receiving Post Facilitation Stretching along with the same conventional therapy. The intervention will be conducted for 4 weeks, with 3 sessions per week on alternate days, each session lasting approximately 45 minutes. Outcome measures will include: Pain intensity assessed using the Visual Analogue Scale (VAS) Cervical range of motion measured using a goniometer Functional disability assessed using the Neck Disability Index (NDI) This study aims to determine the more effective stretching technique for reducing pain, improving cervical mobility, and enhancing functional outcomes, thereby supporting evidence-based physiotherapy practice in managing cervical radicular pain.
Eligibility Criteria
Inclusion Criteria: 1. Both male and female gender 2. Age 30 to 60 years with a +ve spurling test and radiating arm pain for more than 4 weeks 3. Unilateral cervical radicular pain 4. +ve upper limb tension test and neck disability index \<50% Exclusion Criteria: 1. History of cervical spinal surgery 2. Severe facet joint osteoarthritis 3. History of fracture in the head and neck region 4. Patient with cognitive dysfunction or mental illness, severe cardiovascular, cerebrovascular, liver, or kidney dysfunction 5. History of dizziness, vertigo, and vomiting 6. Osteoporosis and prolonged use of steroids 7. Cervical myelopathy, tumor, or infectious disease
Contact & Investigator
Shoaib Waqas
STUDY CHAIR
Lahore University of Biological and Applied Sciences
Frequently Asked Questions
Who can join the NCT07724470 clinical trial?
This trial is open to participants of all sexes, aged 30 Years or older, up to 60 Years, studying Cervical Radicular Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07724470 currently recruiting?
Yes, NCT07724470 is actively recruiting participants. Contact the research team at muhammad.tariq@ubas.edu.pk for enrollment information.
Where is the NCT07724470 trial being conducted?
This trial is being conducted at Lahore, Pakistan, Lahore, Pakistan.
Who is sponsoring the NCT07724470 clinical trial?
NCT07724470 is sponsored by Lahore University of Biological and Applied Sciences. The principal investigator is Shoaib Waqas at Lahore University of Biological and Applied Sciences. The trial plans to enroll 40 participants.