Effectiveness and cost-effectiveness of Pain Rehabilitation Programs (PRP) for patients with chronic musculoskeletal pain: less is better?

Completed

• Conditions: chronic pain; non-malignant pain; 10028302

• Registration Number: NL-OMON36237
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 276

Inclusion Criteria

Patients 1. are referred to the 12,16 or 20 weeks Pain Rehabiltiaton Program (PRP) at the UMCG, 2. have chronic musculoskeletal pain (CMP), 3. experience disability caused by CMP, 4. attend no other kinds of treatment, 5. are 18 years or older, 6. are willing to participate in the study, 7. WPN 3 and 4. Defined as:the social and psychosocial factors are complex and relevant regarding maintaining pain related disability.

Exclusion Criteria

Patients 1. are included for 8 weeks of PRP 2. are not willing to participate in the study, 3. are unable to understand the Dutch language, 4. have relevant comorbidities.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Pain related disability, measured with the Pain Disability Index, will be the<br /><br>main outcome.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>For cost-effectiveness direct and indirect costs will be calculated.</p><br>