Individually Tailored Web-based Multimodal Pain Rehabilitation in Primary Health Care
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Luleå Tekniska Universitet
- Enrollment
- 109
- Locations
- 1
- Primary Endpoint
- Work ability
Study Overview
Brief Summary
The aim is to evaluate effects of early individually tailored web-based multimodal rehabilitation for persons with musculoskeletal neck/shoulder and back disorders in primary health care. The aim is also to study if this early web-based pain rehabilitation program is more cost-effective than only multimodal rehabilitation. Randomization will be done at each primary health care centre after screening to 1) Multimodal pain rehabilitation with web-based education and coaching support or 2) multimodal pain rehabilitation. The investigators suggest a clear rehabilitation chain where a web-based program is developed,evaluated and ready to implement if it shows positive effects on work-ability and/or is cost-effective. The research and implementation will be performed in a close cooperation with Luleå University of Technology.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to 63 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •With persistent neuromusculoskeletal pain from the neck/shoulder/back-area and/or fibromyalgia and a screening
- •> 90 on Lintons´ questionnaire, The Örebro Musculoskeletal Pain Questionnaire (Linton & Halldén., 1998; Hockings et.al., 2008)
- •Fluent in Swedish language
- •Working, or in disposition to at least 25%
- •Exclusion Criteria are persons with:
- •Restricted cognitive functioning
- •Comorbidity which might prevent treatment participation
- •Identified abuse, retirement pension
- •Ongoing causal treatment
- •Pregnancy
- •Patients lacking internet attached computers in their home
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Work ability
Time Frame: 4 month
Secondary Outcomes
- Self-efficacy in relation to workability(12 month)
- General health(12 month)
- Functional status(12 month)
- Pain rating(12 month)
Investigators
Peter Michaelson
Senior lecturer
Luleå Tekniska Universitet