Conjoint Analysis of Treatment Preferences for Osteoarthritis
Osteoarthritis
About this trial
This is an observational trial for Osteoarthritis focused on measuring Knee pain, osteoarthritis, non-surgical treatment, age 65+
Eligibility Criteria
Inclusion Criteria:
- Age 65 or older
- Knee pain over the past month on most days
- Able to travel to Family Medicine offices, if in the treatment group
- Able to read and understand English
- Able to answer questions on a computer screen
Exclusion Criteria:
- Bleeding or non-bleeding ulcer within the last year
- History of ruptured ulcer (ever)
- History of GI bleeding (ever)
- Currently taking Coumadin or blood-thinning medication
- Diagnosis of lupus (ever), psoriatic arthritis (ever), gout (current or within past year), rheumatoid arthritis (ever), or coronary artery disease (ever)
- Prior total knee replacement or scheduled to get knee replacement in painful knee(s)
- Satisfied with current knee pain treatment
- Unable to get to a doctor for knee pain if needed
Sites / Locations
- Baylor College of Medicine Family Medicine
Arms of the Study
Arm 1
Arm 2
Usual Care
Conjoint Analysis Group
Patients randomized to the control group will be sent the post-test measures suitably modified to reflect the fact that they did not participate in the conjoint analysis program. Four weeks after the post-test measures are completed, a staff member will call the subject to complete a 10 minute follow-up questionnaire to assess if any changes in treatment have occurred and to take further measurements (same measurements given to treatment group).
Patients randomized to the experimental group will meet the research staff to complete the conjoint analysis software and post-test measures. The post-test measures include preparedness for decision-making, personal uncertainty, osteoarthritis knowledge, arthritis self-efficacy, and satisfaction with the results of the conjoint analysis program. The in-person visit takes approximately 60 minutes to complete. Four weeks after the in-person visit, a staff member will call the subject to complete a 10 minute follow-up questionnaire to assess if any changes in treatment have occurred and to take further measurements (i.e. global pain assessment, arthritis self-efficacy, personal uncertainty, and osteoarthritis knowledge).