Interdisciplinary Rehabilitation of Patients With Chronic Widespread Pain
NCT ID: NCT01352052
Last Updated: 2016-08-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
192 participants
INTERVENTIONAL
2011-05-31
2014-01-31
Brief Summary
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Detailed Description
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Currently there are no official recommendations concerning the diagnosing and management of patients suffering from CWP in the European health care system. The complexity of the condition underlines the necessity of a comprehensive multi-dimensional assessment and a patient-focused multi-component intervention.
The present study is a prospective, pragmatic randomized controlled trial (RCT), with blinded outcome assessors, aiming to evaluate the outcome of an interdisciplinary multi-component rehabilitation programme customized to patients with CWP and focusing on functional ability and adaptations in everyday life. 176 patients with CWP recruited from the department of rheumatology at Frederiksberg Hospital will be consecutively enrolled in the study over a 1-year period. Participants will be randomized to a 2-weeks non-residential, group-based, multi-component treatment course conducted by an interdisciplinary team or 6-months waiting list for the same course.
The instrumentation for intervention planning, as well as for outcome evaluation, will be based on an ICF measurement framework, as recommended by WHO and performance-based assessment of functional ability (AMPS) and self-reported, health-related quality of life (SF-36) will be applied as primary outcome measures.
Overall, the study results is expected to contribute to the development of more cost-effective health care strategies aiming at prevention of mal-adaptive illness behaviour and progressive functional loss in patients suffering from CWP.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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waiting list assignment
6 months waiting list assignment followed by the 2-week interdisciplinary rehabilitation programme
No interventions assigned to this group
Intervention: interdisciplinary rehabilitation programme
A two-weeks non-residential, group-based, psycho-educative treatment course conducted by an interdisciplinary team.
interdisciplinary rehabilitation
A two-weeks non-residential, group-based, psycho-educative, multi-component treatment course conducted by an interdisciplinary team consisting of a rheumatologist, a nurse, occupational therapists, physical therapists, and a psychologist. The rehabilitation Programme comprises of a combination of lectures and group discussions, as well as instructions during physical exercise and task performance. The main focus is on education and adaptations in everyday life. There is a scheduled Programme for every day, with a daily time schedule between four and six hours. There will be a maximum of eight participants in each group.
Interventions
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interdisciplinary rehabilitation
A two-weeks non-residential, group-based, psycho-educative, multi-component treatment course conducted by an interdisciplinary team consisting of a rheumatologist, a nurse, occupational therapists, physical therapists, and a psychologist. The rehabilitation Programme comprises of a combination of lectures and group discussions, as well as instructions during physical exercise and task performance. The main focus is on education and adaptations in everyday life. There is a scheduled Programme for every day, with a daily time schedule between four and six hours. There will be a maximum of eight participants in each group.
Eligibility Criteria
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Inclusion Criteria
* fulfills the American College of Rheumatology (ACR) 1990 classification criteria of widespread musculoskeletal pain i.e. reporting of pain axially and in all 4 body quadrants for a minimum duration of 3 months
* willing to participate in a 2-week group-based rehabilitation programme
Exclusion Criteria
* concurrent history of major psychiatric disorder not related to the pain disorder
* other medical conditions capable of causing patients symptoms (e.g. uncontrolled inflammatory/autoimmune disorder, uncontrolled endocrine disorder, malignancy)
* not Danish speaking
* enrollment in any other clinical trial within the last 30 days
18 Years
FEMALE
No
Sponsors
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Oak Foundation
OTHER
Frederiksberg University Hospital
OTHER
Responsible Party
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Henning Bliddal
Professor
Principal Investigators
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Bente Danneskiold-Samsøe, Professor
Role: STUDY_DIRECTOR
The Parker Institute, Frederiksberg University Hospital
Kirstine Amris, MD
Role: PRINCIPAL_INVESTIGATOR
The Parker Institute, Frederiksberg University Hospital
Locations
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The Parker Institute, Frederiksberg Hospital
Frederiksberg, Frederiksberg, Denmark
The Parker Institute, Frederiksberg University Hospital
Frederiksberg, , Denmark
Countries
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References
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Amris K, Jespersen A, Bliddal H. Self-reported somatosensory symptoms of neuropathic pain in fibromyalgia and chronic widespread pain correlate with tender point count and pressure-pain thresholds. Pain. 2010 Dec;151(3):664-669. doi: 10.1016/j.pain.2010.08.023. Epub 2010 Sep 15.
Waehrens EE, Amris K, Fisher AG. Performance-based assessment of activities of daily living (ADL) ability among women with chronic widespread pain. Pain. 2010 Sep;150(3):535-541. doi: 10.1016/j.pain.2010.06.008. Epub 2010 Jul 3.
Jespersen A, Dreyer L, Kendall S, Graven-Nielsen T, Arendt-Nielsen L, Bliddal H, Danneskiold-Samsoe B. Computerized cuff pressure algometry: A new method to assess deep-tissue hypersensitivity in fibromyalgia. Pain. 2007 Sep;131(1-2):57-62. doi: 10.1016/j.pain.2006.12.012. Epub 2007 Jan 25.
Related Links
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Web page of the Parker Institute, Frederiksberg University Hospital, Denmark
Other Identifiers
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BDS-2011-099
Identifier Type: -
Identifier Source: org_study_id
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