N/A Completed N=54 Randomized Other

Postoperative Virtual Clinical Encounters

Source: ClinicalTrials.gov NCT04138810 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Aug 2020

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

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.

Outcome Measures

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

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. Informational only — not medical advice.