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Cluster randomised double-blind pilot and feasibility trial of an active behavioural physiotherapy intervention for acute nonspecific neck pain: a mixed method

Cluster randomised double-blind pilot and feasibility trial of an active behavioural physiotherapy intervention for acute nonspecific neck pain: a mixed method

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180607001
Enrollment
60
Registered
2018-06-07
Start date
2019-02-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute non&#45

Interventions

The ABPI is developed through the modified Delphi study and social cognitive theory focusing on self&#45
efficacy enhancement. The ABPI consists of 4 phases in terms of the promotion of understanding&#44
maturity&#44
stamina&#44
and coping.,Participants will be managed according to current practice reflecting the recommendations provided in the clinical nonspecific neck pain guidelines.
Experimental Other,Active Comparator Other
Active Behavioural Physiotherapy Intervention (ABPI),Usual care

Sponsors

-
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Participants aged 18-60 years presenting with nonspecific neck pain within the previous 4 weeks.

Exclusion criteria

Exclusion criteria: Signs and symptoms of upper cervical instability, cervical artery dysfunction, WAD, suspected serious spinal pathology, open wounds, 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, previously symptomatic degenerative diseases of the cervical spine or neck pain within 6 months prior to the recruitment, alcohol abuse, dementia, serious mental diseases, psychiatric diseases, osteoporosis, serious medical conditions (e.g. severe diabetes and hypertension) and/or non-Thai speaking and reading.

Design outcomes

Primary

MeasureTime frame
Neck Disability Index 2 Questionnaire

Secondary

MeasureTime frame
Numerical Rating Scale for pain intensity 2 Scale,Cervical Range of Motion (CROM) 2 Clinical assessment,EuroQol-5 Dimensions 2 Questionnaire,Fear Avoidance Beliefs Questionnaire 2 Questionnaire

Countries

Thailand

Contacts

Public ContactTaweewat Wiangkham

Department of Physical Therapy, Faculty of Allied Health Sciences, Naresuan University, Phitsanulok,

taweewatw@nu.ac.th0908918669

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026