N/A N=54 Randomized Other

Postoperative Virtual Clinical Encounters

Pelvic Organ Prolapse

Bottom Line

View on ClinicalTrials.gov: NCT04138810 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Aug 2020

Primary outcome: Primary: Patient Satisfaction Via the Patient Satisfaction Questionnaire -18 — 80.7; 81.2 score on a scale

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: VCE (Other); Survey (Other)
Age: Adult, Older Adult · 18+ yrs
Sex: Female
Sponsor: University of Pennsylvania
Primary completion: Jul 2019

Outcome Measures

Outcome	Result	p-value
PRIMARY Patient Satisfaction Via the Patient Satisfaction Questionnaire -18	80.7; 81.2	—

Summary

Postoperative follow up is necessary following any surgical procedure and has been conducted in the same manner since the field of surgery began. The study will determine feasibility and patient satisfaction of innovative postoperative virtual clinical encounters utilizing mobile video conference technology for women undergoing pelvic reconstructive surgery through a randomized controlled trial.

Eligibility Criteria

Inclusion Criteria

Undergoing surgery for pelvic organ prolapse
Age greater than 18
Access to a smartphone
Access to high speed internet access (via 4G or 3G on their smartphone or high speed Wi-Fi)
Signed up for MyPennMedicine web portal
Ability to download MyChart mobile application
Pennsylvania Hospital Subject: NJ or PA resident, HUP & Presbyterian Hospital Subject: PA resident

Exclusion Criteria

Pregnancy
Inability to read, speak or understand English
Isolated midurethral sling procedure
Extraperitoneal vaginal colpopexy with Uphold mesh

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04138810). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.