RECRUITING

Unobtrusive Sensing of Medication Intake ("USE-MI")

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

The purpose of this study is to test the USE-MI system hardware and software to see if it can accurately measure when subjects take their HIV-related medications and help them remember to take these medications. With the use of a smartwatch and smartphone "app", investigators hope to be able to monitor medication adherence in real-time and send subjects electronic reminders when they may have forgotten to take their medication.

Official Title

Unobtrusive Sensing of Medication Intake ("USE-MI")

Quick Facts

Study Start:2019-01-08
Study Completion:2025-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03571022

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 CriteriaExclusion Criteria
  1. * Either a) have an HIV infection and are taking ART, or b) risk factors for contracting HIV infection and are taking PrEP
  2. * Taking their medications from pill bottles, or other containers that the USE-MI system can monitor properly
  3. * Reasonable proficiency in English
  4. * Able to come to the research office for monthly follow-up visits
  1. * Not responsible for taking their own HIV medications (e.g. residing in a supervised setting where their medications are administered to them)
  2. * Taking medications using a method that the USE-MI system cannot monitor properly
  3. * Lacking proficiency in English

Contacts and Locations

Study Contact

Jacob Karr
CONTACT
206-215-4226
jacob.karr@swedish.org

Principal Investigator

Barry Saver, MD
PRINCIPAL_INVESTIGATOR
Swedish Medical Center
Jenna Marquard, PhD
PRINCIPAL_INVESTIGATOR
University of Massachusetts, Amherst

Study Locations (Sites)

Swedish Medical Center
Seattle, Washington, 98122
United States

Collaborators and Investigators

Sponsor: Swedish Medical Center

  • Barry Saver, MD, PRINCIPAL_INVESTIGATOR, Swedish Medical Center
  • Jenna Marquard, PhD, PRINCIPAL_INVESTIGATOR, University of Massachusetts, Amherst

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 Date2019-01-08
Study Completion Date2025-12-31

Study Record Updates

Study Start Date2019-01-08
Study Completion Date2025-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Medication Adherence