Wellness Program for Depression and Anxiety in Surgical Patients
What You Need to Know Before You Apply
What is the purpose of this trial?
In this study, the investigators will evaluate the feasibility of the Wellness Program, including patient recruitment, screening and outcome measures, and feasibility of adapting the intervention with older Black surgical patients who endorse clinically significant symptoms of depression and/or anxiety.
Who Is on the Research Team?
Joanna Abraham, Ph.D., FACMI, FAMIA
Principal Investigator
Washington University School of Medicine
Are You a Good Fit for This Trial?
This trial is for older Black surgical patients who are experiencing noticeable symptoms of depression and/or anxiety. The study aims to assess the practicality of a Wellness Program designed specifically for them.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Wellness Program
Trial Overview
The focus is on testing the feasibility of a Wellness Program tailored for Black patients undergoing surgery, with an emphasis on recruitment, screening processes, outcome measures, and adaptability of the intervention.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Enrolled participants will participate in the study for approximately 3 months after surgery. The participants will complete questionnaires at baseline, 1 month after surgery, and 3 months after surgery. The Wellness Program will consist of Cognitive Behavioral Therapy (CBT) and medication optimization.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Washington University School of Medicine
Lead Sponsor
The Foundation for Barnes-Jewish Hospital
Collaborator
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