Knee Osteoarthritis Clinical Trial
— STARTOfficial title:
The STavanger osteoARThritis Study in Primary Health Care
Verified date | January 2018 |
Source | Diakonhjemmet Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The START study will implement osteoarthritis (OA) treatment recommendations to increase the use of recommended treatment modalities and reduce non-desired events (e.g. unnecessary referrals to secondary care, unnecessary use of costly imaging modalities and use of treatment modalities supported by low quality of evidence). The purpose of the STavanger osteoARThritis (START) study is to improve the quality of OA care and increase the collaboration between health care professionals in primary health care and across health care levels.
Status | Completed |
Enrollment | 330 |
Est. completion date | November 2017 |
Est. primary completion date | November 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - PT working in private practice in Stavanger Municipality - GP working in Stavanger Municipality - Person with complaints due to hip and/or knee osteoarthritis referred to physiotherapy in Stavanger Municipality - Person with complaints due to hip and/or knee osteoarthritis referred for assessment of joint replacement at Stavanger University Hospital Exclusion Criteria: - Persons referred to physiotherapy after a total joint replacement - Persons who do not understand the Norwegian language - Persons with cognitive dysfunction |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Diakonhjemmet Hospital | Helse Stavanger HF, Stavanger Municipality |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in patient-reported quality of osteoarthritis care | Using the "OsteoArthritis Quality Indicator questionnaire" | 8 weeks pre-implementation vs. 8 weeks post-implementation | |
Secondary | Change in the number of PT discharge summaries to the referring GP | 8 weeks pre-implementation vs. 8 weeks post-implementation | ||
Secondary | Change in the proportion of people with OA referred to orthopaedic surgeon in secondary care that has explored non-surgical treatment modalities beforehand | 8 weeks pre-implementation vs. 8 weeks post-implementation | ||
Secondary | Change in the proportion of people with OA referred to orthopaedic surgeon in secondary care that has taken an MRI and/or conventional radiographs for OA assessment | 8 weeks pre-implementation vs. 8 weeks post-implementation | ||
Secondary | Change in the proportion of people with OA referred to orthopaedic surgeon in secondary care that leads to scheduled joint surgery | 8 weeks pre-implementation vs. 8 weeks post-implementation |
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