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The Impact of a Redesigned Handout for Robotic Sacrocolpopexy on Patient Preoperative Preparedness and Satisfaction

NCT06934304 · University of Texas Southwestern Medical Center · Updated 18 April 2025

What is being tested
new preoperative handout; old preoperative handout
For
Pelvic Organ Prolapse; Patient Satisfaction
Kind of study
Tests a treatment or device on volunteers. No drug phase (a device or procedure study).
Who can join
Ages 18 years and older. About 51 people. The full rules are on the registry page.
Where
United States
When
Starts or started 1 Aug 2022, ends 31 Dec 2023. Registered 18 April 2025.
Results
None posted yet.

In the researchers' words

The goal of this clinical trial is to learn if a new preoperative handout for patients undergoing robotic sacrocolpopexy will improve patient sense of preparedness and satisfaction in comparison to the previously used handout. The main questions it aims to answer are: * Does the new preoperative handout for patients undergoing robotic sacrocolpopexy improve patient preparedness and satisfaction? * Will the new preoperative handout for patients undergoing robotic sacrocolpopexy impact postoperative queries in the form of phone calls and messages to the clinic? Participants will: * Receive routine counseling regarding robotic sacrocolpopexy from their surgeon * Be randomized to the new or old preoperative handout * Undergo robotic sacrocolpopexy * Complete a questionnaire at their 4 week postoperative follow up visit regarding their sense of preparedness for surgery and overall satisfaction
ClinicalTrials.gov, NCT06934304

Sites

  • University of Texas Southwestern Medical CenterDallas, Texas, United States