Cornell Translational Behavioral Science Research Consortium: Angioplasty Qualitative Study

Completed

• Conditions: Angioplasty Patients

• Registration Number: NCT00161603
• Lead Sponsor: Weill Medical College of Cornell University

Brief Summary

To explore and illuminate the cultural, social, and psychological factors that either facilitate or serve as barriers to behavioral change in angioplasty patients. Through a series of open-ended questions we will explore and build a better understanding of how culturally different patient groups perceive heart disease and the difficulties in changing health behavior. In addition, we hope to better understand and anticipate barriers and issues that participants face in successfully changing their behaviors.

Detailed Description

1. To explore and illuminate the cultural, social, and psychological factors that either facilitate or serve as barriers to behavioral change in angioplasty patients. Through a series of open-ended questions we will explore and build a better understanding of how culturally different patient groups perceive heart disease and the difficulties in changing health behavior. In addition, we hope to better understand and anticipate barriers and issues that participants face in successfully changing their behaviors.

2. To use the responses obtained in the qualitative interviews to inform how we should operationalize and tailor the positive affect induction and self-affirmation intervention methods in each of the populations under study. Specifically, this involves assessing what small gifts participants prefer to receive and what would be most effective in inducing positive affect.

Study Timeline

• Study Start: 2003-04
• Study Completion: 2003-09
• Study First Submitted: 2005-09-08
• Study First Submitted QC: 2005-09-11
• Study First Posted: 2005-09-12
• Status Verified: 2008-04
• Last Update Submitted: 2008-04-01
• Last Update Posted: 2008-04-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

• Post-angioplasty patients who had previously participated in an RCT designed to motivate multi-behavior change.

Exclusion Criteria

• Patients who refuse to be interviewed, Patients who were not enrolled in the parent trial

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

The New York Presbyterian Hospital-Weill Medical Center; 🇺🇸 New York, New York, United States