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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00803491
Other study ID # FOUS08001
Secondary ID
Status Active, not recruiting
Phase N/A
First received December 4, 2008
Last updated August 17, 2010
Start date December 2008
Est. completion date February 2013

Study information

Verified date August 2010
Source Spenshult Hospital
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Interventional

Clinical Trial Summary

Randomized controlled trial including 200 subjects with rheumatic diseases. Subjects will be randomized to either a self-promoting problem based learning (PBL) program or a control group with traditional care. The hypothesis is that a PBL program will improve health-related quality of life, empowerment and self-care ability.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 200
Est. completion date February 2013
Est. primary completion date February 2010
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Subjects should have one or several rheumatic diseases diagnosed more than a year.

- Subjects should have musculoskeletal pain, sleep disturbances and fatigue, overwhelming number of days during the last three months.

- Subjects should be registered on the waiting list to the rheumatologic clinic.

Exclusion Criteria:

- Subjects with difficulties speaking and/or read Swedish.

- Subjects with difficulties travelling to the clinic.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Other:
Problem based learning
Group sessions under supervision from a nurse. Each group including 8 subjects. 10 occasions during a period of one year.
Traditional rheumatology care.
Individually base.

Locations

Country Name City State
Sweden Spenshult Hospital Oskarström

Sponsors (3)

Lead Sponsor Collaborator
Spenshult Hospital County Council of Halland, Sweden, The Swedish Rheumatism Ass

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Health related quality of life as measured by SF-36 Baseline, after intervention and six, twelve and thirtysix months after No
Secondary Empowerment as measured by ASES-S Baseline, after intervention and six, twelve and thirtysix months after No
Secondary Empowerment measured by SWE-RES-23. Baseline, after intervention and six, twelve and thirtysix months after No
Secondary Self-care ability measured by ASA-A. Baseline, after intervention and six, twelve and thirtysix months after No
Secondary Sense of coherence (SOC). Baseline, after intervention and six, twelve and thirtysix months after No
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