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Health Related Quality of Life After a Self-promoting Learning Program for People With Rheumatic Diseases

Health Related Quality of Life After a Self-promoting Problem-based Learning Program for People With Rheumatic Diseases: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00803491
Enrollment
200
Registered
2008-12-05
Start date
2008-12-31
Completion date
2013-02-28
Last updated
2010-08-18

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

Conditions

Rheumatic Diseases

Keywords

Rheumatic diseases, Problem based learning, Health-related quality of life, Empowerment, Self-care

Brief 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.

Interventions

OTHERProblem based learning

Group sessions under supervision from a nurse. Each group including 8 subjects. 10 occasions during a period of one year.

OTHERTraditional rheumatology care.

Individually base.

Sponsors

The Swedish Rheumatism Ass
CollaboratorOTHER
County Council of Halland, Sweden
CollaboratorOTHER_GOV
Spenshult Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Health related quality of life as measured by SF-36Baseline, after intervention and six, twelve and thirtysix months after

Secondary

MeasureTime frame
Empowerment as measured by ASES-SBaseline, after intervention and six, twelve and thirtysix months after
Empowerment measured by SWE-RES-23.Baseline, after intervention and six, twelve and thirtysix months after
Self-care ability measured by ASA-A.Baseline, after intervention and six, twelve and thirtysix months after
Sense of coherence (SOC).Baseline, after intervention and six, twelve and thirtysix months after

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026