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

Sponsor
Alberta Bone and Joint Health Institute (Other)
Overall Status
Completed
CT.gov ID
NCT00297726
Collaborator
(none)
64
18

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Self-Management Program
N/A

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 Design

Study Type:
Interventional
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Single
Primary Purpose:
Educational/Counseling/Training
Official Title:
A Prospective Study to Examine the Efficacy of the Arthritis Self Management Program (ASMP) in Patients With Osteoarthritis (OA) in Alberta
Study Start Date :
Oct 1, 2004
Study Completion Date :
Apr 1, 2006

Outcome Measures

Primary Outcome Measures

  1. A difference in the WOMAC score of 20 percentage points []

Secondary Outcome Measures

  1. A change in health care provider and medication utilization. []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Alberta Bone and Joint Health Institute

Investigators

  • Principal Investigator: Cyril B Frank, MD, University of Calgary

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00297726
Other Study ID Numbers:
  • PRO-OA-00001
First Posted:
Mar 1, 2006
Last Update Posted:
Mar 1, 2006
Last Verified:
Feb 1, 2006

Study Results

No Results Posted as of Mar 1, 2006