Clinical trial Recruiting at 1 site Interventional Ages 40 to 60

Effectiveness of deep cervical flexor training with or without scapular stabilization in cervical spondylosis

Official title: Effectiveness of Pressure Biofeedback-Assisted Deep Cervical Flexor Training With and Without Scapular Stabilization Exercises on Pain, Range of Motion and Neck Disability in Cervical Spondylosis

Run by Ibadat International University, Islamabad · NCT07814833 · Data updated 2026-11-12

This study tests whether adding scapular stabilization to pressure biofeedback-assisted neck exercise improves pain, neck movement, and disability in people with cervical spondylosis.

Quick facts

Study typeInterventional
Ages40 Years to 60 Years
SexAll
Enrollment44 (estimated)
SponsorIbadat International University, Islamabad
Academic / other
Locations1 site (Rawalpindi, Punjab Province)
StatusRecruiting
StartedJune 3, 2026
Main results expectedSeptember 15, 2026
Study endsSeptember 24, 2026
Registry record updatedSeptember 28, 2026
Trial IDNCT07814833 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 40–60 with chronic neck pain and radiologically confirmed cervical spondylosis, able to perform active neck and shoulder movements, and willing to comply with the protocol.

Probably not a fit

Patients with recent neck surgery, severe neurological symptoms, inflammatory or systemic musculoskeletal diseases, or those already in structured neck/shoulder rehab may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial compares two approaches to treating chronic neck pain due to cervical spondylosis: pressure biofeedback-assisted deep cervical flexor training with scapular stabilization plus standard physiotherapy, versus the same neck training without scapular stabilization plus standard physiotherapy. Forty-four participants aged 40 to 60 with radiologically confirmed cervical spondylosis will be randomly assigned to the two groups and followed for four weeks of treatment, with sessions three times weekly. Outcomes include pain intensity, cervical range of motion, and neck disability, measured at baseline and after the intervention. The study uses sealed envelope randomization and accounts for a 10% dropout rate.

Why it matters

Potential benefit: If successful, the combined approach could offer greater relief from neck pain and improved function for people with cervical spondylosis.

How similar studies have gone: Previous studies using targeted neck muscle training with biofeedback have shown benefits; however, the addition of scapular stabilization for this condition is less established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Both genders aged 40-60 years.
* Presence of chronic neck pain for ≥3 months with NPRS ≥3.
* Radiologically confirmed cervical spondylosis, including cervical spine X-ray showing disc space narrowing and/or osteophyte formation.
* Ability to perform active cervical and shoulder movements without neurological deficits.
* Willingness to participate in the study and comply with the intervention protocol.

Exclusion Criteria:

* History of cervical spine surgery or trauma in the past 6 months.
* Severe neurological involvement, including cervical myelopathy or severe radiculopathy with motor weakness, gait disturbance, or bowel/bladder involvement.
* Inflammatory or systemic musculoskeletal disorders, e.g., rheumatoid arthritis or ankylosing spondylitis.
* Current participation in structured neck/shoulder rehabilitation programs.
* Uncontrolled medical conditions contraindicating exercise, e.g., uncontrolled hypertension or cardiovascular disease.

Where it's running

  • Hope Physiotherapy Clinic
    Rawalpindi, Punjab Province, Pakistan
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.