The ROAM Research Study Therapy (LTOT) Version

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.

Conditions

Pulmonary Disease, Chronic Obstructive

Study Overview

Study Details

Study overview

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.

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

The ROAM Research Study Therapy (LTOT) Version

Condition
Pulmonary Disease, Chronic Obstructive
Intervention / Treatment

-

Contacts and Locations

Charlottesville

University of Virginia, Charlottesville, Virginia, United States, 22903

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Race demographics of the recruitment area reflect the population of the Charlottesville Metropolitan Statistical Area (MSA).
  • * Due to underrepresentation in local demographics, special effort (via targeted advertising) will be made to recruit Hispanic participants to better match national percentages.
  • * Participants with medical history of COPD
  • * Subjects has to have a prescription for oxygen use via nasal cannula or mask at home
  • * At baseline of health with no hospitalization/exacerbation within the past 6 weeks
  • * Use of Continuous oxygen at baseline
  • * Intermittent oxygen use at home
  • * Inability to understand simple instructions
  • * No respiratory infections and exacerbation within 6 weeks of study

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Virginia,

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

Study Record Dates

2030-12