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Study Summary
No. 2006-0610:.......Bone......Maria Suarez-Almazor......General Internal Medicine/Ambulatory Treatment & Emergency Care
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Study Summary Title
Study Summary
Number:
2006-0610
Study Title:Cognitive Behavioral Determinants in Knee Replacement
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Physician New Patient Referral
Name:Maria Suarez-AlmazorPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:General Internal Medicine/Ambulatory Treatment & Emergency CareReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-745-7670
Contact us about clinical trials
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General Information
Disease Group:BoneSupported By:N/A
Phase of Study:Phase IIReturn
Visit:
The participants are not MDACC patients. However, they are expected to return
for post-op assessments by their orthopedic surgeons at 1, 2, and 6 weeks
post-op at SLEH and Kelsey Seybold clinics.
Treatment
Agents:
NoneHome Care:The patients are expected to receive post-surgical physical therapy for
individually recommended duration of time.
Treatment Loc:Independent Multicenter Arrangements
Estimated
Length of Stay
in Houston:
Total knee replacement patients are usually expected to stay between two and
five days post surgery.
Description/
Intervention:
Unavailable
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Study Objectives / Outcomes
The purpose of the study is to identify the beliefs, attitudes, and behaviors of patients undergoing knee surgery so as to propose modifying factors that will help patients to have the most successful post-operative outcomes. These modifying factors will be identified in Phases I and II, and used in Phase III through patient education of post-surgical recommendations.

This proposal will be conducted in these phases. Phase 1-Aim 1: To identify beliefs, expectations and goals of patients undergoing total knee arthroplasty (TKA). Aim 2: To determine which are appropriate and realistic goals for patients undergoing knee arthroplasty. Phase 2-Aim 3: To develop an instrument to evaluate patient beliefs, expectations and goals in relation to knee arthroplasty. Aim 4: To identify psychosocial and educational barriers to surgical success and patient satisfaction after knee arthroplasty. Aim 5: To evaluate the impact of psychological determinants, and knee arthroplasty outcomes on health costs . Hypotheses: 1.Patient expectancies of improvement, high self-efficacy, and rational goals are associated with better outcomes in knee arthroplasty. 2.Psychosocial/educational barriers and poor functional outcomes are associated with increased health costs in patients undergoing knee arthroplasty. Phase 3: Aim 6 :To develop and pilot test a patient-centered, cognitive behavioral and psychoeducational intervention for patients undergoing TKA, with the goal of maximizing functional outcomes and patient satisfaction.

K-24 is a mentoring career award (2006-0627). Please note that there is no funding for this study from K-24, which only funds Dr. Suarez-Almazor's mentoring activities.
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Study Status Information
Study Activation / Registration Date:09/07/2006
IRB Review and Approval Date:08/01/2006
Study Type:Observational
Recruitment Status:Open
Projected Accrual:310
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Radiologic diagnosis of knee osteoarthritis

2) First knee arthroplasty (previous hip replacements will be allowed)

3) Adequate cognitive status as determined by Folstein's Mini Mental Status questionnaire

4) Age 40 years or older

5) Living in the community at the time of the surgery (as opposed to long-term care facilities)

6) Ability to communicate in English language without a translator

7) Have access to a telephone

8) Consent to participate

Exclusion Criteria:1) Revision surgery

2) Inflammatory arthropathies (e.g. rheumatoid arthritis)

3) Neurological disorders

4) Paget's syndrome or metabolic bone disorders

5) Litigation process related to surgery

6) Patients seeking or receiving workers' compensation benefits

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Links
Registration Number: Not Applicable Clinical Trial

Other Links:
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Results


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