Does a Virtual Coach Offer a Better Solution for Weight Reduction in Ventral Hernia Patients With Obesity?

Last updated: April 17, 2025
Sponsor: University of Florida
Overall Status: Completed

Phase

N/A

Condition

Weight Loss

Obesity

Diabetes Prevention

Treatment

MyChart enabled virtual weight loss coach

Standard preoperative weight loss tools

Clinical Study ID

NCT05797974
202300391
UL1TR001427
  • Ages 18-90
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The purpose for this research is to create a MyChart-enabled virtual coach that assists obese patients lose weight prior to ventral hernia surgery. Researchers intend to show how the use of a virtual coach is more effective in preoperative weight reduction prior to ventral hernia repair over usual care. Correspondingly, this may lower unplanned hospital readmissions. For this clinical trial, where randomization is not possible, the study team will implement the use of propensity score matching that sorts individuals into different study arms as if randomly assigned. The primary outcome is the average net amount of time-dependent weight change per group over six months. Secondary outcomes are for the intervention group, patient satisfaction with the virtual coach and for both groups, quality of life. In addition, areas of social and economic disadvantage will be identified that may contribute to higher obesity rates. Machine learning (ML) modeling will be used to determine the important features for weight lost over the course of the study. The impact of this work will be to demonstrate efficacy and realized workflow efficiencies within a hospital-based surgery clinic.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Subjects between 18 and 90 years of age with a Body Mass Index (BMI) of 30 and aboveand diagnosed with Obesity by the ICD 10 Code: E66.9 who have been evaluated by asurgeon and offered elective ventral hernia repair. Also, participants must have acomplete medical record that allows for all statistical calculations to beperformed.

Exclusion

Exclusion Criteria:

  • Pregnant females, patients with severe mental disorders, prescribed psychiatricmedications associated with weight gain, a history of a Substance Use Disorder,patients on long-term steroid therapy, and patients with insufficient medicalrecords.

Study Design

Total Participants: 33
Treatment Group(s): 2
Primary Treatment: MyChart enabled virtual weight loss coach
Phase:
Study Start date:
February 01, 2024
Estimated Completion Date:
March 01, 2025

Connect with a study center

  • University of Florida Jacksonville

    Jacksonville, Florida 32209
    United States

    Site Not Available

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