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

Not yet recruitingNot applicableNCT07132229
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

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

Study details

Official title
Impact of Cervical High-Intensity Resistive Exercises on Ventilatory Measures in Patients With Chronic Non-Specific Neck Pain
Interventions
Sponsor
Cairo University
Start date
2025-08-10
Primary completion
2026-02-01
Sex
All
Age range
from 20 Years to 40 Years
Results posted
No results posted in this snapshot
Countries
Egypt
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Thirty-four patients diagnosed CNSNP. 2. Age of the patients between 20-40 years. 3. Non-specific neck pain started more than 3 months. 4. Reduce ventilatory function; FVC \>= 70% from predicted. 5. Waist to height ratio (WtHR)\> 60 %. 6. Positive craniocervical flexion test. 7. Positive neck flexor endurance test. 8. Pain at neck after prolonged static weight bearing positions. 9. Pain with palpation of the neck paraspinal or suboccipital or trapezius muscles. Exclusion Criteria: 1. History of whiplash injury. 2. Clinical sign of cervical radiculopathy. 3. Clinical signs of cervical myelopathy. 4. Rheumatoid Arthritis or any other autoimmune diseases. 5. Any respiratory disorders. 6. Tumors. 7. vertebrobasilar insufficiency VBI.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07132229