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Individually Tailored Web-based Multimodal Pain Rehabilitation in Primary Health Care

Individually Tailored Web-based Multimodal Pain Rehabilitation in Primary Health Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01475591
Enrollment
109
Registered
2011-11-21
Start date
2011-10-31
Completion date
2015-06-30
Last updated
2016-09-23

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

Conditions

Musculoskeletal Pain

Keywords

persistent neuromusculoskeletal pain, neck, shoulder, back-area, risk, longlasting, pain syndrome

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.

Interventions

BEHAVIORALWeb-based multimodal rehabilitation based on cognitive based principles

The patient will be randomized to either the interventions group (multimodal pain rehabilitation with an added web-based multimodal rehabilitation with CBT-influences) or a control group (multimodal pain rehabilitation).

Sponsors

Norrbottens County Council
CollaboratorOTHER_GOV
Luleå Tekniska Universitet
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 63 Years
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: * Dementia * 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

Design outcomes

Primary

MeasureTime frame
Work ability4 month

Secondary

MeasureTime frameDescription
Pain rating12 monthPain-rating is measured on a visual analog-scale
Self-efficacy in relation to workability12 monthSelf-efficacy in relation to work-ability is measured by a questionnarie
General health12 monthGeneral health is measured with SF-36 and EQ-5D.
Functional status12 monthFunctional status is measured with Pain disability index.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026