RECRUITING

The ROAM Research Study Therapy (LTOT) Version

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 research is to test a device being developed that can see how patients use oxygen therapy over a long period of time. This study will focus on developing a new display part called ROAM module which will be attached to your oxygen source. The display will provide easily-accessible information that can show how you interact with your supplies and the oxygen machine automatically without connecting the oxygen source to the internet or other devices.

Official Title

The Respiratory Oxygen Adherence Monitor System for COPD With Long Term Oxygen Therapy

Quick Facts

Study Start:2025-01-14
Study Completion:2030-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06810323

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Race demographics of the recruitment area reflect the population of the Charlottesville Metropolitan Statistical Area (MSA).
  2. * Due to underrepresentation in local demographics, special effort (via targeted advertising) will be made to recruit Hispanic participants to better match national percentages.
  3. * Participants with medical history of COPD
  4. * Subjects has to have a prescription for oxygen use via nasal cannula or mask at home
  5. * At baseline of health with no hospitalization/exacerbation within the past 6 weeks
  6. * Use of Continuous oxygen at baseline
  1. * Intermittent oxygen use at home
  2. * Inability to understand simple instructions
  3. * No respiratory infections and exacerbation within 6 weeks of study

Contacts and Locations

Study Contact

Roselove NUNOO-ASARE, MA
CONTACT
434-243-6074
RNN3B@VIRGINIA.EDU
Carol Bampoe, BS
CONTACT
cb3ff@virginia.edu

Principal Investigator

Yun M Shim, MD
PRINCIPAL_INVESTIGATOR
Division of Pulmonary and Critical Medicine

Study Locations (Sites)

University of Virginia
Charlottesville, Virginia, 22903
United States

Collaborators and Investigators

Sponsor: University of Virginia

  • Yun M Shim, MD, PRINCIPAL_INVESTIGATOR, Division of Pulmonary and Critical Medicine

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 Date2025-01-14
Study Completion Date2030-12

Study Record Updates

Study Start Date2025-01-14
Study Completion Date2030-12

Terms related to this study

Additional Relevant MeSH Terms

  • Pulmonary Disease, Chronic Obstructive