Actively Recruiting

Age: 18Years +
All Genders
ID07471464

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) during initial consultation

Preoperative Counseling

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

Surgery and Immediate Post-operative Care

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

Postoperative Follow-up

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

Monitoring

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

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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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