Evaluation of COPD Co-Pilot
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Chronic Obstructive Pulmonary Disease |
| Therapuetic Areas: | Pulmonary / Respiratory Diseases |
| Healthy: | No |
| Age Range: | 35 - Any |
| Updated: | 4/17/2018 |
| Start Date: | January 2017 |
| End Date: | March 2018 |
The purpose of undertaking this study is to examine the use of COPD Co-PilotTM, a COPD
disease management program manufactured and operated by HGE Health Care Solutions, LLC, in
COPD patients outside of the geographic base of HGE's existing patient population
(Philadelphia, PA). The purpose is to demonstrate the feasibility of expanding the program to
additional geographic sites and to examine whether similar outcome measures are achieved in
patients under the supervision of health care providers that are new to the program.
disease management program manufactured and operated by HGE Health Care Solutions, LLC, in
COPD patients outside of the geographic base of HGE's existing patient population
(Philadelphia, PA). The purpose is to demonstrate the feasibility of expanding the program to
additional geographic sites and to examine whether similar outcome measures are achieved in
patients under the supervision of health care providers that are new to the program.
Inclusion Criteria:
1. Subject has read, understood and signed an informed consent form prior to enrollment.
2. Males or females age ≥35 years old
3. Documented diagnosis of moderate to very severe COPD (GOLD Level II-IV)
4. Must be able to read and understand English and consent for themselves
5. Subject is willing and able to use an iPad mini device.
Exclusion Criteria:
1. Subject has a cognitive impairment (determined by physician) that will make it hard to
follow instructions regarding device usage
2. Subject is currently known to suffer from or have a history of significant substance
abuse within the last 2 years
3. Subject has any condition that in the opinion of the provider may adversely affect
their participation
4. Subject is residing in hospice care, Skilled Nursing Facilities or Long Term Acute
Care facilities
5. Subject has a planned procedures at time of enrollment that will occur within
timeframe of study that will require hospitalization or otherwise adversely affect
their ability to participate
6. Subject has no cellular coverage at their primary residence
7. Subject plans to travel to a location with no cellular coverage for a significant
period (>1 week) during their program participation
We found this trial at
1
site
171 Ashley Avenue
Charleston, South Carolina 29425
Charleston, South Carolina 29425
843-792-1414
Medical University of South Carolina The Medical University of South Carolina (MUSC) has grown from...
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