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

A

Alberta Bone and Joint Health Institute

Status

Completed

Conditions

Osteoarthritis

Treatments

Behavioral: Self-Management Program

Study type

Interventional

Funder types

Other

Identifiers

NCT00297726
PRO-OA-00001

Details and patient eligibility

About

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.

Full 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.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Educational/Counseling/Training

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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