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PREPARE- pre-pain rehabilitation treatment, in chronic non-specific musculoskeletal pain patients.

PREPARE- (Cost-)effectiveness of a pre-pain rehabilitation treatment, a Motivational interviewing (MI)-based nurse-led intervention in chronic non-specific musculoskeletal pain patients: A randomized controlled trial (RCT).

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29174
Enrollment
184
Registered
2011-09-12
Start date
2011-10-15
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Motivational interviewing, Chronic non-specific pain, Rehabilitation

Interventions

2 appointments each lasting 45 min up to 1h with a trained nurse take place at the department of rehabilitation medicine: 1. In the MIP intervention condition, the sessions are based on Motivational
2. In the UC control condition, health information and health education around chronic pain and pain rehabilitation is provided. Both interventions are provided by separately trained nurses each prov

Sponsors

Maastricht University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Non-specific chronic musculoskeletal pain syndrome; 2. Pain duration >3 months; 3. Over 18 years of age, max. 65 years; 4. Eligible and (as yet) indicated for outpatient pain rehabilitation treatment, main indication criteria: Chronic pain; 5. Adequate literacy to complete assessment measures.

Exclusion criteria

Exclusion criteria: 1. Pregnancy; 2. Surgery planned in the foreseeable future; 3. Patient involved in litigation procedures; 4. Psychopathology which makes the indication for the pain rehabilitation treatment impossible.

Design outcomes

Primary

MeasureTime frame
Participation measured by the USER-P.

Secondary

MeasureTime frame
1. Adherence; 2. Drop-out; 3. Physical functioning (PDI); 4. Quality of life (SF-36); 5. Client-centeredness (CCCQ); 6. Credibility of the treatment (CEQ); 7. Self-efficacy (DGSE); 8. Self-reported main complaints (PSC).

Contacts

Public ContactVera-Christina Mertens

Maastricht University Faculty of Health, Medicine and Life Sciences (FHML) Department of Rehabilitation Medicine Postbus 616

Vera.Mertens@maastrichtuniversity.nl+31 (0)43 3882160

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)