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N/A N=53 Randomized Health Services Research

Utilizing Telemedicine for Delivery of Postoperative Care

Laparoscopic Gynecologic Surgery

Enrolled (actual)
53
Serious AEs
0.0%
Results posted
Jul 2020
Primary outcome: Primary: PSQ-18 General Satisfaction — 4.0; 4.5 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Telemedicine (Other); Office visit (Other)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
Texas Tech University Health Sciences Center, El Paso
Primary completion
May 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
PSQ-18 General Satisfaction
4.0; 4.5
PRIMARY
PSQ-18 Technical Quality
4.0; 4.5
PRIMARY
PSQ-18 Interpersonal Manner
4.0; 4.5
PRIMARY
PSQ-18 Communication
4.5; 4.5
PRIMARY
PSQ-18 Time Spent With Doctor
4.0; 4.5
PRIMARY
PSQ-18 Accessibility and Convenience
4.0; 4.0
SECONDARY
Actual Visit Time
9.2; 9.1
SECONDARY
Visits to Emergency Department
1; 0
SECONDARY
Phone-calls to Office
6; 5
SECONDARY
Time Dedicated by Patient to Complete Visit
60.8; 14.7
SECONDARY
Number of Patients Who Desired to Switch Groups
2; 0

Summary

The investigators propose a pilot project in which enrolled patients undergoing major gynecologic surgery will be randomized to either a traditional office postoperative visit or a telemedicine postoperative visit. The two groups will then be compared on a variety of metrics including clinical outcomes, patient satisfaction and time.

Eligibility Criteria

Inclusion criteria

  • Female patients between ages 18-60
  • Have access to smart-phone with video/audio and internet capabilities
  • Undergoing laparoscopic gynecologic surgery that requires a postoperative visit
  • Total laparoscopic hysterectomy
  • Laparoscopic removal of adnexal structures
  • Laparoscopic excision of endometriosis

Exclusion criteria

  • Patient unwilling to participate
  • The patient is unwilling to install and utilize the telemedicine app on their smartphone.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04348357). 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.

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