Comparative Effectiveness Randomised Controlled Trial of Hybrid Muscle Conditioning

NCT ID
NCT07837414
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
The Hong Kong Polytechnic University
Conditions
Chronic Nonspecific Neck Pain

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Powering Exercise-induced Hypoalgesia and Functional Recovery in Chronic Nonspecific Neck Pain by Hybrid Muscle Conditioning: a Comparative Effectiveness Randomised Controlled Trial With Mechanistic Analysis

Enrollment: 210 participants (Estimated).

What is being studied

  • Other: Endurance exercise group
  • Other: Hybrid exercise group
  • Other: Motor control exercise group

Who may be eligible

Ages
18 Years to 50 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * adults aged 18-50 years * unilateral CNSNP of more than 3 months' duration with mechanical nature (neck pain provoked or aggravated by cervical posture or movement) * baseline neck pain ≥3/10 on Numerical Pain Rating Scale (NPRS) * baseline functional disability ≤25/50 on Neck Disability Index (NDI) * baseline funcctional diability ≤60/100 on Disabilities of the Arm, Shoulder and Hand (DASH) * impaired deep cervical flexor performance verified by \<26 mmHg on craniocervical flexion test (CCFT) activation score (Jull et al., 2004) * positive scapular reposition test verified by an immediate reduction in pain or improvement in cervical range of motion during manual scapular repositioning (Van Dillen et al., 2007; Wannaprom et al., 2021) Exclusion Criteria: * neck pain caused by trauma or with a specific diagnosis (including radiculopathy, disc herniation, or spinal stenosis, or if neurological deficits or congenital cervical deformity) * history of previous surgery of the cervical or thoracic spine or shoulder * marked restriction of cervical mobility verified by extension \<30° or rotation \<60° (Cleland et al., 2010; Wainner et al., 2003) * inability to achieve full shoulder elevation required for the prescribed exercise * BMI ≥25 kg/m² * comoborities orthopaedic, neurological, or systemic conditions * high fear-avoidance beliefs verified by Tampa Scale for Kinesiophobia score ≥37 (Vlaeyen and Linton, 2000); psychological distress (SF-12 Mental Component Summary score ≤40) (Yu et al., 2015) * regular use of analgesics, muscle relaxants, or vasoactive medications * dizziness or vertigo suggestive of vestibular dysfunction or vertebrobasilar insufficiency * any contraindications to electrical stimulation for muscle endurance index measurement (any mental or neural implant, seizure)

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Hong Kong

Sample of listed locations

  • The Hong Kong Polytechnic University — Hong Kong, Hong Kong — Site recruitment status not specified in the registry data

Study details

Start date
October 5, 2026
Primary completion date
December 31, 2029
Completion date
June 30, 2030
First posted
September 23, 2026
Collaborators
Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong, University of Birmingham

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07837414
Registry last updated
September 23, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07837414 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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