Remote Telemonitoring to Improve Prehabilitation and Surgical Outcomes of Patients Undergoing Elective Abdominal Surgery

NCT03706963 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 169

Last updated 2022-12-12

No results posted yet for this study

Summary

There is data confirming that simple tests of physical capability, such as the timed "get-up-and-go" test and the 6-minute walk test, correlate with surgical outcomes. It is reasonable to assume that preoperative telemonitoring, which allows for the tracking of more variables over a wider range of activities, could provide a significantly more accurate picture of a patient's physical fitness than a short one-time test performed in the clinic setting.

Almost half of the patients who are readmitted at Washington University are readmitted for less than 4 days. The readmitted patients usually present with sepsis, are treated with antibiotics and percutaneous drainage, and are discharged home relatively quickly. Earlier identification of these patients, prior to the development of sepsis, would reduce the risks to the patient and allow for outpatient management.

Conditions

  • Abdominal Surgery

Interventions

OTHER

Phone Call

-phone call 7 days (+/- 2 days) into preoperative period

Sponsors & Collaborators

  • The Foundation for Barnes-Jewish Hospital

    collaborator OTHER
  • BJC Innovative Lab

    collaborator UNKNOWN
  • Washington University School of Medicine

    lead OTHER

Principal Investigators

  • Chet Hammill, M.D., MCR, FACS · Washington University School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-15
Primary Completion
2022-07-10
Completion
2022-07-10

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03706963 on ClinicalTrials.gov