Actively Recruiting
Centered Surgery - Preoperative Counseling and Patient Satisfaction for Urogynecology Prolapse Surgeries
Led by The Cleveland Clinic · Updated on 2026-03-13
106
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating patient satisfaction and preparedness for urogynecology prolapse surgeries by comparing two methods of preoperative counseling: standard individual phone calls and virtual group sessions called Shared Medical Appointments (SMAs). This prospective cohort study aims to determine if virtual group counseling improves patient satisfaction and preparedness, while also assessing healthcare resource use after surgery. The study is conducted at Cleveland Clinic and focuses on patients undergoing major prolapse surgeries. Participants receive preoperative counseling either through individual nursing telehealth calls or virtual group nursing appointments. The study will recruit over 24 months, with follow-up lasting until the postoperative visit 7 to 9 weeks after surgery. Eligible surgeries include vaginal colpopexy, vaginal hysteropexy, laparoscopic sacrocolpopexy, and others, possibly combined with additional procedures. Participants complete surveys before and after surgery to measure satisfaction and preparedness. During the study, participants complete electronic surveys using validated tools like the Patient Satisfaction Questionnaire-18 (PSQ-18) and the Patient Preparedness Questionnaire (PPQ). Data collection is managed through REDCap and linked to electronic health records. Researchers will analyze satisfaction scores and healthcare use, including phone calls, unscheduled visits, and hospital readmissions, up to 12 weeks post-surgery. The study plans to enroll about 106 participants, with data securely stored and privacy protected throughout.
CONDITIONS
Brief Title
Centered Surgery - Preoperative Counseling and Patient Satisfaction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Has decision-making capacity and able to provide informed consent for research participation
- For patients undergoing Shared Medical Appointments: Has active MyChart access
- Able to speak and read English
You will not qualify if you...
- Unable to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) during initial consultation
Duration - Up to the day of surgery
Participants receive preoperative nursing counseling either through individual phone calls or virtual shared medical appointments to prepare for surgery.
1 or more telehealth or virtual group appointments before surgery
Duration - Day of surgery plus immediate recovery period
Participants undergo urogynecology prolapse surgery and receive immediate post-operative care.
1 surgical procedure visit plus hospital stay as applicable
Duration - 6 to 9 weeks after surgery
Participants attend a postoperative visit to assess recovery, patient satisfaction, and healthcare resource utilization.
1 in-person postoperative visit
Duration - Up to 12 weeks after surgery
Participants are observed for healthcare resource utilization such as patient-initiated phone calls, unscheduled office visits, emergency room visits, and readmissions up to 12 weeks following surgery.
No scheduled visits; ongoing monitoring via medical records and surveys
Trial Site Locations
Total: 1 location
1
Cleveland Clinic
Cleveland, Ohio, United States, 44195
Actively Recruiting
Research Team
P
Petrina LaFaire, MD, MS
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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