Skip to content

Telemedicine Use in Preoperative Counseling for Endometrial Cancer Survivors

A Randomized, Controlled Trial for Asynchronous Telemedicine Use in Preoperative Counseling for Individuals With Endometrial Cancer

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05712668
Enrollment
100
Registered
2023-02-03
Start date
2022-05-09
Completion date
2025-05-31
Last updated
2024-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Counseling, Telemedicine

Keywords

Telemedicine, Preoperative Counseling

Brief summary

To determine whether telemedicine is an acceptable addition to pre-operative counseling, compared to face-to-face communication alone for patients with endometrial cancer.

Detailed description

Newly diagnosed endometrial cancer survivors, who are presenting for their initial consultation with a plan for minimally invasive surgery, will be randomized 1:1 to standard counseling or standard counseling plus asynchronous telemedicine video. The asynchronous video will be available outside of the office and can be viewed multiple times. The primary endpoint is patient anxiety, measured via the State-Trait Anxiety Inventory (STAI) questionnaire, assessed before surgery. The secondary outcomes of anxiety following surgery as well as patient satisfaction with counseling type (measured via the Patient Satisfaction Questionnaire (PSQ-18)) before and after surgery will be compared between groups. Both groups will complete questionnaires following their initial consultation (but before surgery) and at their post-operative visit. For the telemedicine group, the duration and frequency of video views will be collected. Participants completing both surveys will receive a survivorship gift bag.

Interventions

Providers will review the diagnosis, surgical planning, risks/benefits/alternatives to surgery, post-operative care, and long term scope of care.

BEHAVIORALAsynchronous telemedicine

An asynchronous video will be delivered by Mytonomy. This platform allows investigators to track user analytics relating to the time, frequency, or duration watched by the user.

Sponsors

Virginia Polytechnic Institute and State University
CollaboratorOTHER
Carilion Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

A total of 100 patients will be enrolled and randomized if they meet the inclusion criteria. Fifty patients allocated will be allocated to receive pre-operative counseling via standard face-to-face care and 50 patients allocated to receive standard pre-operative counseling with the addition of asynchronous telemedicine.

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

1. Patients with clinical stage I histologically confirmed endometrial carcinoma, which is clinically confined to the uterus and comprises approximately two-thirds of all endometrial carcinoma cases 2. Patients undergoing planned minimally invasive surgical procedures, such as a minimally invasive technique such as conventional laparoscopy or robotic-assisted laparoscopy, as part of treatment at the Division of Gynecologic Oncology at Carilion Clinic, Roanoke, VA 3. Internet/cellular access at home 4. Ability to read and comprehend materials on questionnaires

Exclusion criteria

1 Patients that do not meet the inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Anxiety related to preoperative counselingFollowing the initial office visit or online viewing session, prior to surgeryIt will be measured via the State-Trait Anxiety Inventory (STAI) questionnaire, a validated tool used in clinical settings to diagnose anxiety and to distinguish it from depressive syndromes. STAI is comprised of 20 concise questions on a 4-point Likert scale.

Secondary

MeasureTime frameDescription
Patient satisfaction with preoperative counselingFollowing the initial office visit or online viewing session, prior to surgeryIt will be measured via the Patient Satisfaction Questionnaire (PSQ-18), which is also a validated questionnaire. It is comprised of 18 questions, also on a Likert scale, used to assess 7 dimensions of patient satisfaction.
Patient satisfaction with preoperative counseling, surgical impactAt the postoperative exam, approximately 2-4 weeks from surgeryIt will be measured via the Patient Satisfaction Questionnaire (PSQ-18), which is also a validated questionnaire. It is comprised of 18 questions, also on a Likert scale, used to assess 7 dimensions of patient satisfaction.
Anxiety related to preoperative counseling, surgical impactAt the postoperative exam, approximately 2-4 weeks from surgeryIt will be measured via the State-Trait Anxiety Inventory (STAI) questionnaire, a validated tool used in clinical settings to diagnose anxiety and to distinguish it from depressive syndromes. STAI is comprised of 20 concise questions on a 4-point Likert scale.

Countries

United States

Contacts

Primary ContactShannon Armbruster, MD
sdarmbruster@carilionclinic.org(540) 581-0275
Backup ContactCaroline Kim
hkim@carilionclinic.org

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026