A Pilot Prospective Clinical Trial Using Remote Monitoring for Cancer Patients Undergoing Outpatient Chemotherapy

Sponsor
Inova Health Care Services (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06106360
Collaborator
(none)
100
1
11.7
8.6

Study Details

Study Description

Brief Summary

A pilot study using remote monitoring technology developed by Locus Health in cancer patients undergoing chemotherapy treatment.

Condition or Disease Intervention/Treatment Phase
  • Device: Locus Health iPhone App

Detailed Description

Modern-day wearable devices, such as Apple Watches or Fitbits, are widely available, non-invasive, and can provide continuous vital sign monitoring for the early detection of potential health complications. Early detection of things such as fever or increased heart rate can alert patients to seek medical attention sooner and therefore have the potential to improve patient outcomes and decrease healthcare costs.

To further investigate the feasibility of using remote patient monitoring ( RPM)to prospectively monitor patients undergoing outpatient chemotherapy for chemotherapy related toxicities, defined as follows: (1) patients answer queries through the Locus Health iPhone app at least 70% of the time; (2) patients report that the Locus Health iPhone app and the Apple Watch were 'easy to use,' defined as an average score of 7 or higher on the first two questions of the post-intervention questionnaire, and (3) fewer than 10% of patients withdraw from the study.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Pilot Prospective Clinical Trial Using Remote Patient Monitoring for Cancer Patients Undergoing Outpatient Chemotherapy
Anticipated Study Start Date :
Oct 31, 2023
Anticipated Primary Completion Date :
Jan 31, 2024
Anticipated Study Completion Date :
Oct 20, 2024

Arms and Interventions

Arm Intervention/Treatment
3 Cohorts

Cohort 1: Daily from day 2 through the end of treatment cycle (n=34) Cohort 2: Daily days 2-9 then every third day through end of cycle (n=33) Cohort 3: Daily days 2-9 for all symptoms, every third day thereafter regarding 'pain' only through end of cycle (n=33)

Device: Locus Health iPhone App
In this pilot study patients are enrolled into three (3) different groups which will vary by the frequency of the queries being sent to the patients during their chemotherapy cycle. The patients will be separated into three groups of 33-34 patients each. Each group will have a different frequency of symptom questions sent to them via the Locus Health iPhone App to determine patient fatigue and the compliance impact of different query cadences. Patients will be assigned to these 3 groups sequentially since the platform could not assign patients to these three cohorts in a random manner.

Outcome Measures

Primary Outcome Measures

  1. Participants' use of Locus Heath iPhone App and the Apple Watch to monitor chemotherapy related toxicities [120 days or until the chemotherapy regimen has stopped, whichever is sooner]

    The remote monitoring technology (the Locus Heath iPhone App and the Apple Watch) is being used to prospectively monitor patients undergoing outpatient chemotherapy for chemotherapy related toxicities, defined as at least 80% of patients wear the watch at least 70% of the time during waking hours.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Planned to be treated with a new cytotoxic chemotherapy or chemoimmunotherapy regimen for a solid tumor or malignant hematology condition for at least 4 months

  • ECOG performance status of 0-2

  • Age of 18 or older patient with any solid tumor or hematologic malignancy

  • English or Spanish speaker

  • Own an Apple iPhone

  • Capacity and willingness to provide informed consent

Exclusion Criteria:
  • Patients undergoing concurrent radiation since they will be seen on a daily basis by clinic care teams and are not likely to benefit from active remote patient monitoring

  • Patients unwilling or unable to comply with the protocol, including wearing the Apple Watch (including recharging daily) and answering queries on the Locus Health iPhone application per the protocol and study group cadence

  • Any condition for which in the Investigator's opinion would limit compliance with study requirements

Contacts and Locations

Locations

Site City State Country Postal Code
1 Inova Schar Cancer Institute Fairfax Virginia United States 22031

Sponsors and Collaborators

  • Inova Health Care Services

Investigators

  • Principal Investigator: John Deeken, MD, Inova Schar Cancer Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Inova Health Care Services
ClinicalTrials.gov Identifier:
NCT06106360
Other Study ID Numbers:
  • U23-08-5132
First Posted:
Oct 30, 2023
Last Update Posted:
Oct 30, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Inova Health Care Services
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 30, 2023