NCT06934304

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

Randomized Controlled Study on Patient Preoperative Preparedness and Satisfaction Using a Redesigned Handout for Robotic Sacrocolpopexy

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 51 (actual)
• Sponsor: University of Texas Southwestern Medical Center · Academic / Other
• Sex: Female
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

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

Conditions

• Pelvic Organ Prolapse
• Patient Satisfaction

Interventions

Type	Name	Description
OTHER	new preoperative handout	A new preoperative handout for robotic sacrocolpopexy was designed at a lower reading level and providing more perioperative details
OTHER	old preoperative handout	The old or standard preoperative handout for robotic sacrocolpopexy

Timeline

• Start date: 2022-08-01
• Primary completion: 2023-12-31
• Completion: 2023-12-31
• First posted: 2025-04-18
• Last updated: 2025-04-18

Locations

1 site across 1 country: United States