Psychology of Minimally Invasive Surgical Scars

Obesity Clinical Trial

Official title: Psychology of Minimally Invasive Surgical Scars

Status Terminated

Clinical Trial Summary

The purpose of this study is to examine the psychological and psychosocial impact of surgical scars after minimally invasive surgery (MIS). 100 adult patients who are about to undergo bariatric procedures through the Duke Metabolic & Weight Loss Surgery program will be enrolled in this study. 50 patients will be randomly assigned to standard laparoscopic surgery and 50 will be assigned to the percutaneous group. All patients will complete pre-operative psychometric testing to establish a baseline body-image score as well as a patient's initial subjective perceptions around surgery and surgical scars. Follow-up visits will be done at standard of care timepoints - 3 weeks, 3 and 6 months, and 1 year after surgery. Subjects will complete the same psychometric measures to identify differences in psychological and psychosocial responses to standard laparoscopic and percutaneous scars. Patients will also complete a measure on scar satisfaction. The investigators hope to identify any differences between standard laparoscopic versus percutaneous approaches.

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Obesity

• NCT number: NCT03004560
• Study type: Interventional
• Source: Duke University
• Status: Terminated
• Phase: N/A
• Start date: January 2017
• Completion date: December 31, 2019