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Virtual vs In-Person Visits for Post-Operative Satisfaction

N/A
Recruiting
Led By Rosanne Kho, M.D.
Research Sponsored by The Cleveland Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2-weeks
Awards & highlights

Study Summary

This trial is comparing the safety and effectiveness of post-operative visits done virtually to in-person visits for patients who had a minimally invasive hysterectomy. The goal is to see if virtual visits are just as good as in-person visits when it comes to patient satisfaction.

Who is the study for?
This trial is for patients over 18 who have had a minimally invasive hysterectomy and can give informed consent. They must speak English and have access to technology like a phone or computer for virtual visits. It's not suitable for those where the surgeon advises against virtual follow-up, suspects cancer, or if they can't consent or lack tech access.Check my eligibility
What is being tested?
The study compares patient satisfaction between virtual postoperative visits and in-office ones after minimally invasive hysterectomy. Satisfaction is measured using surveys, with secondary focus on new post-op complications requiring treatment, additional office visits, urgent care/ER trips, no-show rates, visit duration, and travel distance.See study design
What are the potential side effects?
There are no direct medical side effects from participating in this trial as it involves comparing types of appointments rather than medications. However, potential issues could include miscommunication leading to delayed diagnosis of complications such as infections or wound healing problems.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2-weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 2-weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Patient satisfaction at 2-weeks
Secondary outcome measures
Post-operative complications
Other outcome measures
Unscheduled visits

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Virtual visitExperimental Treatment1 Intervention
Patients will have 2-week post-operative virtual visit
Group II: Office visitActive Control1 Intervention
Patients will return to the office for a 2-week post-operative visit

Find a Location

Who is running the clinical trial?

The Cleveland ClinicLead Sponsor
1,027 Previous Clinical Trials
1,364,098 Total Patients Enrolled
Rosanne Kho, M.D.Principal InvestigatorThe Cleveland Clinic
1 Previous Clinical Trials
22 Total Patients Enrolled

Media Library

Virtual visit Clinical Trial Eligibility Overview. Trial Name: NCT04855708 — N/A
Patient Satisfaction Research Study Groups: Office visit, Virtual visit
Patient Satisfaction Clinical Trial 2023: Virtual visit Highlights & Side Effects. Trial Name: NCT04855708 — N/A
Virtual visit 2023 Treatment Timeline for Medical Study. Trial Name: NCT04855708 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are individuals still able to apply for this research?

"As per clinicaltrials.gov, this trial is actively soliciting applicants. It was first posted on February 5th 2021 and most recently edited on July 11th 2022."

Answered by AI

What is the current enrollment of this research endeavor?

"Affirmative. According to the information presented on clinicaltrials.gov, this medical study is presently searching for 180 volunteers from a single site. The trial was first introduced on February 5th 2021 and has been updated as recently as July 11th 2022."

Answered by AI
~43 spots leftby Apr 2025