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NCT Number: NCT07132229

Impact Of Cervical High-Intensity Resistive Exercises In Patients With Chronic Non-Specific Neck Pain

Purposes of the study

To investigate the effect of adding Cervical High-Intensity Resistive Exercises to conventional physical therapy in patients with Chronic Non-Specific Neck Pain

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Key information

Age range

20 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Patients will be randomized into either Cervical High-Intensity Resistive Exercises group or Conventional physical therapy group. Patients will receive the intervention for six weeks. Outcomes will be assessed at baseline and post-intervention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Thirty-four patients diagnosed CNSNP.
  • Age of the patients between 20-40 years.
  • Non-specific neck pain started more than 3 months.
  • Reduce ventilatory function; FVC >= 70% from predicted.
  • Waist to height ratio (WtHR)> 60 %.
  • Positive craniocervical flexion test.
  • Positive neck flexor endurance test.
  • Pain at neck after prolonged static weight bearing positions.
  • Pain with palpation of the neck paraspinal or suboccipital or trapezius muscles.

Exclusion criteria

  • History of whiplash injury.
  • Clinical sign of cervical radiculopathy.
  • Clinical signs of cervical myelopathy.
  • Rheumatoid Arthritis or any other autoimmune diseases.
  • Any respiratory disorders.
  • Tumors.
  • vertebrobasilar insufficiency VBI.

Treatment and study plan

Cervical High-Intensity Resistive Exercises

Other

The patient will wear a neck harness, and a weight equivalent to 90% of the patient's measured maximum voluntary isometric contraction (MVIC) will be attached to it.

Conventional physical therapy

Other

Conventional physical therapy consisting of TENS for pain control, soft tissue release for the cervical and associated muscles, activation and strengthening exercises for the deep neck flexors, extensors, and scapular muscles, as well as diaphragmatic breathing exercises.

Primary outcomes

  1. Disability

    Time frame: Change from Baseline Disability at 6 weeks

    Neck disability index (NDI)

  2. Diaphragm thickness

    Time frame: Change from Baseline Diaphragm thickness at 6 weeks

    Ultrasound

  3. Forced vital capacity (FVC)

    Time frame: Change from Baseline Forced vital capacity (FVC) at 6 weeks

    Spirometry

  4. maximum voluntary ventilation (MVV)

    Time frame: Change from maximum voluntary ventilation (MVV) at 6 weeks

    Spirometry

Secondary outcomes

  1. Neck pain

    Time frame: Change from Baseline Neck pain at 6 weeks

    Visual analogue scale

  2. Strength of neck flexors, extensors, and side bending

    Time frame: Change from Baseline Strength of neck flexors, extensors, and side bending at 6 weeks

    Hand-held dynamometer (HHD)

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Impact of Cervical High-Intensity Resistive Exercises on Ventilatory Measures in Patients With Chronic Non-Specific Neck Pain

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Aug 20, 2025
Registry last updated
Aug 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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