RECRUITING

ALgorithms Adapted From Remote Monitoring

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

ALgorithms Adapted From Remote Monitoring

Quick Facts

Study Start:2023-02-20

Study Completion:2025-07

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05782140

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion 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.	* \<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.

Inclusion Criteria

Exclusion 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.

* \<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.

Contacts and Locations

Study Contact

Karlyn Pierson, MAN, RN

CONTACT

507-538-1960

pierson.akrlyn@mayo.edu

Principal Investigator

Janani Reisenauer, MD

PRINCIPAL_INVESTIGATOR

Mayo Clinic

Study Locations (Sites)

Mayo Clinic in Rochester

Rochester, Minnesota, 55905

United States

Collaborators and Investigators

Sponsor: Mayo Clinic

Janani Reisenauer, MD, PRINCIPAL_INVESTIGATOR, Mayo Clinic

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-02-20

Study Completion Date2025-07

Study Record Updates

Study Start Date2023-02-20

Study Completion Date2025-07

Terms related to this study

Keywords Provided by Researchers

Remote Monitoring

Additional Relevant MeSH Terms

Surgery