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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-60
SponsorIbadat International University, Islamabad

About this trial

This randomized controlled trial will evaluate the effectiveness of pressure biofeedback-assisted deep cervical flexor training with and without scapular stabilization exercises in patients with cervical spondylosis. The study will compare the effects of the two treatment approaches on pain intensity, cervical range of motion and neck disability.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pressure Biofeedback-Assisted Deep Cervical Flexor Training

    Other intervention

    Deep cervical flexor (DCF) training will be performed using a pressure biofeedback unit to facilitate selective activation of the longus colli and longus capitis. Participants will lie supine with hips and knees flexed, with the cuff placed beneath the cervical spine at C4-C5 and inflated to a baseline pressure of 20 mmHg. Gentle cranio-cervical flexion will be performed by nodding and drawing the chin inward while maintaining head contact with the surface and avoiding compensatory superficial muscle activation. Target pressure will progress from 22 mmHg in Week 1 to 24, 26, and 28 mmHg in Weeks 2-4, respectively. Training will consist of 3 sets of 10 repetitions, with 5-second holds in Week 1 progressing to 10-second holds thereafter and 30-60 seconds of rest between sets. Arm lifts will be added in Week 3 and leg marching in Week 4. The intervention will be administered three times weekly for four consecutive weeks.

  • Scapular Stabilization Exercises

    Other intervention

    Scapular stabilization exercises will be performed progressively for 4 weeks to improve scapular control, alignment, and stabilizer strength. In Week 1, seated scapular retraction and depression will be performed for 3 sets of 10 repetitions with 5-second holds and 60 seconds rest. In Week 2, scapular retraction will progress using light TheraBand resistance for 3 sets of 10 repetitions with controlled movement. In Week 3, wall slides and prone Y and T raises will be performed for 3 sets of 8-10 repetitions. In Week 4, scapular stabilization with shoulder flexion and abduction will be performed for 3 sets of 10 repetitions. All exercises will emphasize controlled movement, neutral alignment, and avoidance of compensatory shoulder or trunk movements. Sessions will be conducted three times weekly.

  • Standard Physiotherapy

    Other intervention

    Standard physiotherapy will include therapeutic exercises and postural management techniques aimed at reducing pain, improving cervical mobility, flexibility, and functional performance. Cervical range-of-motion exercises including flexion, extension, lateral flexion, and rotation will be performed within a pain-free range for 10 repetitions in each direction. Stretching exercises for the upper trapezius, levator scapulae, and pectoral muscles will be performed for 20-30 seconds for 3 repetitions. Cervical isometric strengthening exercises including flexion, extension, and lateral flexion will be performed with a 5-10-second hold for 10 repetitions. Postural education and ergonomic advice will also be provided, including instructions regarding proper sitting posture, appropriate head and neck positioning, and avoidance of prolonged static postures. Standard physiotherapy will be provided for approximately 10-15 minutes per session, three times weekly for four consecutive weeks.

Treatment groups

44 Participants
are divided into 2 treatment groups
Group A: Group A: Pressure Biofeedback-Assisted Deep Cervical Flexor Training + Scapular Stabilization ExerciExperimental treatment 3 interventions
Group B: Group B: Pressure Biofeedback-Assisted Deep Cervical Flexor Training + Standard PhysiotherapyActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Neck Disability - Neck Disability Index (NDI)

Measure: Functional disability related to neck pain measured using the Neck Disability Index.

Time frame
Baseline and 4 weeks of treatment.
2

Pain Intensity - Numeric Pain Rating Scale (NPRS)

Neck pain intensity measured using the 0-10 Numeric Pain Rating Scale.

Time frame
Baseline and 4 weeks of treatment
3

Universal Goniometer

Measure: Cervical Range of Motion - Cervical flexion, extension, right/left lateral flexion, and right/left rotation.

Time frame
Baseline and 4 weeks of treatment.

Secondary outcomes

1

The Neck Flexor Endurance Test

Measure: Cervical flexor muscle endurance.

Time frame
Baseline and 4 weeks of treatment

Other outcomes

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