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Post-Market Surveillance With a Novel mHealth Platform

CompletedN/A

Sponsor: Yale University

Conditions: Gastrectomy, Atrial Fibrillation

Interventions: A mobile health platform

Countries: United States

This is a study to pilot the feasibility of using a novel patient-led, smartphone-based mobile health platform (Hugo) for real-world surveillance of outcomes of patients after they undergo a bariatric surgical procedure (either sleeve gastrectomy or gastric bypass) and catheter-based atrial fibrillation ablation

Eligibility overview

Sex: ALL

Age: 18 Years to —

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion Criteria:

* Age \>18
* English-speaking
* Planned for either a bariatric surgical procedure (either sleeve gastrectomy or gastric bypass) or catheter-based atrial fibrillation ablation
* Participant is willing and able to read and sign consent and participate in study
* Participant has an email account and a mobile device (smartphone or tablet) able to download the necessary applications
* Participant is willing to use the mobile health platform and syncable devices (e.g. Fitbit Charge 2)
* Attending bariatric surgeon or electrophysiologist (as appropriate) concurs that patient is a candidate for enrollment

Exclusion Criteria:

Healthy patients

Patients who refuse participation

Locations (2)

New Haven, Connecticut, United States
Rochester, Minnesota, United States