ClinicalTrials.Veeva

Menu

ALgorithms Adapted From Remote Monitoring (ALARM)

Mayo Clinic logo

Mayo Clinic

Status

Enrolling

Conditions

Surgery

Treatments

Device: Mayo Clinic Watch Device

Study type

Observational

Funder types

Other

Identifiers

NCT05782140
22-003308

Details and patient eligibility

About

Through the aid of remote monitoring and early symptom detection, a patient's response to stress and normalization to their individual baseline can better contribute towards algorithms which are predictive of clinical decline.

Enrollment

250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years and older
  • Scheduled to undergo surgery resulting in a complex recovery as evaluated by the treating Department of Surgery surgeon. This includes but is not limited to the following inpatient elective surgery procedures: esophagectomy, pancreatectomy, major liver resections, open vascular surgery, lower extremity bypass, colectomy, and complex pulmonary resections (lobes and above).
  • Subjects are committed to daily exercise as outlined in the protocol.

Exclusion criteria

  • <18 years of age
  • Subject is pregnant
  • Subject is dismissed from the hospital to a nursing home or long term care facility.
  • Subject cannot commitment to daily exercise as outlined in the protocol.
  • Subjects enrolled in another device or drug study does not necessarily preclude them from participating in this study. Please check with the PI for inclusion if the subject is on another device or drug study.

Trial design

250 participants in 1 patient group

Mayo Clinic Rochester Surgical Patients
Description:
Mayo Clinic Watch Device
Treatment:
Device: Mayo Clinic Watch Device

Trial contacts and locations

1

Loading...

Central trial contact

Karlyn Pierson, MAN, RN

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems