Centered Surgery - Preoperative Counseling and Patient Satisfaction
Recruiting
Observational Study
Pelvic Organ Prolapse
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
106 (estimated)
Sponsor
The Cleveland Clinic · Other
Who this trial is looking for
This trial is looking for patients who are scheduled for specific pelvic surgeries. Participants will take part in different types of counseling sessions and complete surveys about their satisfaction and preparedness for surgery.
Are You a Good Fit for This Trial?
You may be able to join if
I am over 18 years old
I can make my own medical decisions
I have an active MyChart account for group sessions
I can speak and read English
You may not be able to join if
I am unable to consent
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This study is a prospective cohort study which aims to assess patient satisfaction and preparedness for surgery through two methods of preoperative counseling: standard individual phone calls versus virtual group sessions called Shared Medical Appointments (SMAs). The study will focus on patients undergoing urogynecology prolapse surgeries at Cleveland Clinic. Researchers hypothesize that virtual …
This study is a prospective cohort study which aims to assess patient satisfaction and preparedness for surgery through two methods of preoperative counseling: standard individual phone calls versus virtual group sessions called Shared Medical Appointments (SMAs). The study will focus on patients undergoing urogynecology prolapse surgeries at Cleveland Clinic. Researchers hypothesize that virtual group counseling will improve patient satisfaction and preparedness compared to individual phone calls. Additionally, the study will evaluate healthcare resource utilization as a secondary outcome.
Participants will complete surveys before and after surgery to measure satisfaction and preparedness using validated tools. The study will enroll patients aged 18 and older who can provide informed consent and are scheduled for specific prolapse surgeries. Findings may help improve preoperative counseling practices and enhance patient-centered care.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age \>18y
* Has decision-making capacity and able to provide informed consent for research participation
* For patients undergoing SMA: Has active MyChart
* Able to speak and read English
Exclusion Criteria:
* Unable to consent
Inclusion Criteria:
* Age \>18y
* Has decision-making capacity and able to provide informed consent for research participation
* For patients undergoing SMA: Has active MyChart
* Able to speak and read English
Exclusion Criteria:
* Unable to consent
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