Effectiveness of an active behavioural physiotherapy intervention in patients with chronic non-specific neck pai
Phase 3
- Conditions
- Patients with chronic non-specific neck painNeck pain, clinical trial
- Registration Number
- TCTR20230429001
- Lead Sponsor
- aresuan University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Participants aged 20-70 years presenting with non-specific neck pain at least 12 weeks
Exclusion Criteria
Signs and symptoms WAD or traumatic neck pain,(92) upper cervical instability, cervical artery dysfunction, suspected serious spinal pathology, active inflammatory arthritis, tumours, infection of the skin and soft tissue, bleeding disorders or using anti-coagulant medication, any current or previous treatment from any other third party, or presenting with any serious injuries, history of cervical surgery, neurological conditions, alcohol abuse, dementia, serious mental diseases, psychiatric diseases, osteoporosis, serious medical conditions (e.g. severe diabetes and hypertension), pregnant and/or non-Thai speaking and reading.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method eck Disability Index 2 (baseline and 3-month follow-up post baseline) questionnaire
- Secondary Outcome Measures
Name Time Method umerical Pain Rating Scale 2 (baseline and 3-month follow-up post baseline) questionnaire,Cervical Range of Motion 2 (baseline and 3-month follow-up post baseline) Cervical Range of Motion Device,Fear-Avoidance Beliefs Questionnaire 2 (baseline and 3-month follow-up post baseline) questionnaire,Central Sensitisation Inventory 2 (baseline and 3-month follow-up post baseline) questionnaire,Short Form-36 2 (baseline and 3-month follow-up post baseline) questionnaire