A Study to Examine the Efficacy of the Arthritis Self Management Program

Not Applicable

Completed

• Conditions: Osteoarthritis

• Registration Number: NCT00297726
• Lead Sponsor: Alberta Bone and Joint Health Institute

Brief Summary

This study will examine the efficacy of the Arthritis Self Managemnet Program (ASMP)and determine changes in health resource utilization after completeing the ASMP program.

Detailed Description

This study will provide an analysis of the efficacy of the Arthritis Self Management Program (ASMP) using both patient administered questionnaires as well as the health utilization data maintained within the administrative databases at Alberta Health and Wellness. This study will also provide other information that has not yet been evaluated in other arthritis self management studies including co-morbidity data and other specific health related utilization information that has not yet been evaluated in other arthritis self management studies including co-morbidity data and other specific health related utilization information as it is recorded in administrative databases, will include a control group and will adjust for potential confounding variables such as sex, age, body mass index (BMI) and stage of disease.

Study Timeline

• Study Start: 2004-10
• Status Verified: 2006-02
• Study First Submitted: 2006-02-27
• Study First Submitted QC: 2006-02-27
• Last Update Submitted: 2006-02-27
• Study First Posted: 2006-03-01
• Last Update Posted: 2006-03-01
• Study Completion: 2006-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 64

Inclusion Criteria

• OA of the hip and/or knee
• Patient is 18 years of age and over

Exclusion Criteria

• a concurrent systemic inflammatory disease
• Patient has previously participated in an arthritis self management educational program
• Patient is awaiting total hip or total knee replacement surgery patient has a medical co-morbidity that would render the patient to participate fully in the study procedures, including terminal conditions such as chronic obstructive pulmonary disease, end stage renal disease, heart failure, malignancy with anticipated life expectancy of equal to or less than 2 years
• Patient has been diagnosed with senile dementia or Alzheimer's disease

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
A difference in the WOMAC score of 20 percentage points

Secondary Outcome Measures

Name	Time	Method
A change in health care provider and medication utilization.