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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02333656
Other study ID # 229079
Secondary ID
Status Completed
Phase N/A
First received January 4, 2015
Last updated January 30, 2018
Start date January 2015
Est. completion date October 2017

Study information

Verified date January 2018
Source Diakonhjemmet Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Previous research has shown that the osteoarthritis care for persons with hip or knee osteoarthritis in Norway has a potential for improvement as the provided care may not necessarily reflect evidence-based guideline recommendations. This study will determine if a new model for integrated osteoarthritis (OA) care in primary health care will result in improved quality of osteoarthritis care and health benefits for the patients (reduced pain and body weight, increased function and activity level) among patients with hip and/or knee osteoarthritis. Further, this study will examine if the new model reduce the number of unnecessary referrals to Magnetic Resonance Imaging (MRI) and to orthopaedic surgeons in secondary care, and if it increases the number of referrals to physiotherapy treatment and the number of discharge reports from the physiotherapists to the referring general practitioner.


Description:

A new model for integrated care for patients with hip and/or knee osteoarthritis (OA) in primary care will be developed and implemented. The purpose of the model is to improve quality of OA care in primary health care services by increasing the collaboration between health care professionals and across health care levels, providing an integrated care and a patient pathway, and facilitating an active and healthy lifestyle among individuals with OA. This implementation study represents a collaborative study between six municipalities and a hospital department aiming to fulfill the intentions of the Norwegian Health Care Coordination Reform. The main aim of the present study is to implement and perform process and effect evaluations of this new model for integrated OA care. The study design will be a cluster randomized controlled trial with a stepped wedge design. Six neighboring municipalities will constitute the six clusters, which will switch from control (current OA care) to intervention phase (new OA model) in a randomized order. All municipalities start the trial simultaneously and act as controls until the point in time they are randomized to crossover from control to intervention, and all municipalities have implemented the intervention by the end of inclusion. The method consists of two parts; 1) Identification of barriers/facilitators + development of the model and interventions, 2) Implementation of the new model (interactive workshops) with process and effect evaluations. Participants will be general practitioners and physiotherapists in primary care as well as people with hip or knee OA.


Recruitment information / eligibility

Status Completed
Enrollment 393
Est. completion date October 2017
Est. primary completion date October 2017
Accepts healthy volunteers No
Gender All
Age group 45 Years and older
Eligibility Inclusion Criteria:

- Activity-related hip and/or knee pain/complaints AND

- Clinical signs and symptoms corresponding to hip and/or knee OA OR radiologically diagnosed OA OR Registered in the medical journal with the ICPC codes L89 (osteoarthritis of the hip), L90 (osteoarthritis of knee), L91 (osteoarthritis not classified elsewhere), L13 (hip symptoms/complaints), L15 (knee symptoms/complaints) and/or L20 (joint symptoms/complaints not classified elsewhere).

Exclusion Criteria:

- Total hip or knee replacement in the actual joint(s) and no pain/complaints in the other hip or knee joint(s)

- Inflammatory rheumatic diseases (e.g. rheumatoid arthritis, spondyloarthritis)

- Malignant illness or other major conditions (i.e unstable cardiovascular disorders or lung disease, dementia) that restrict the ability to adhere to the recommended OA treatment

- Do not understand the Norwegian language

Study Design


Intervention

Other:
New OA model
The general practitioners and the physiotherapists will attend an inter-active workshop and deliver osteoarthritis care in line with international recommendations for osteoarthritis treatment. The general practitioner will refer eligible patients to treatment by physiotherapists at "Healthy Living Center" or by physiotherapists in private practice. This treatment will include a standardized patient education program followed by structured exercise program with individual adjustments. The general practitioner will schedule a follow-up after the 12-week treatment and will receive a treatment report from the physiotherapist.

Locations

Country Name City State
Norway Diakonhjemmet Hospital Oslo

Sponsors (2)

Lead Sponsor Collaborator
Diakonhjemmet Hospital The Research Council of Norway

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Osteoarthritis Quality Indicator questionnaire Patient reported achievement of quality indicators for osteoarthritis care 6 months
Secondary Pain Pain level in hip/knee past week 6 months
Secondary Joint stiffness Stiffness in the hip/knee past week 6 months
Secondary Global function Hip/knee function in the past week 6 months
Secondary Patient global assessment of the OA disease 6 months
Secondary Patient Acceptable Symptom State (PASS) 6 months
Secondary Hip/knee function, quality of living subscale Function (Knee injury and Osteoarthritis Outcome Score ADL subscale/ Hip disability and Osteoarthritis Outcome Score OoL subscale (K/HOOS) 6 months
Secondary Physical activity level An index based on self-reported frequency, intensity, duration of physical activity 6 months
Secondary Daily sitting Daily hours in sitting position 6 months
Secondary Satisfaction with the care provided 6 months
Secondary Health related quality of life (EQ-5D) 6 months
Secondary Self-reported body weight 6 months
Secondary Health care use, medication use and sick leave 6 months
Secondary Adverse events Up to 1 year
Secondary Health professionals' knowledge, attitude and behavior in OA care Pre- and post-workshop + 6 months post-workshop
Secondary Referrals to orthopaedic surgeons Number of referrals to secondary care that does not lead to scheduled joint surgery Up to 1 year
Secondary Referrals to MRI Number of referrals to MRI for OA assessment Up to 1 year
Secondary Number of referrals to physiotherapy treatment Up to 1 year
Secondary Discharge reports from physiotherapists Number of discharge reports from PTs at FLSs/ private practice to the referring GP Up to 1 year
Secondary Arthritis Self-efficacy Scale 6 months
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