Personalized Voice Activated Wellness Assistants for Patients With Heart Failure
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Heart Failure
- Sponsor
- Medstar Health Research Institute
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- Change in comfort level using Alexa+ technology as measured by the pre and post-test technology comfort survey
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief Summary
The Alexa+ Study will compare the use of the Amazon Echo Dot with Alexa voice technology in patients with chronic heart failure to those receiving standard of care heart failure management on changes in health and patient-centered outcomes.
Detailed Description
Integrating data from virtual voice activated assistants (Amazon Echo Dot with Alexa voice technology), with the rich medical history available in Electronic Health Records (EHR) will allow a truly customized, interactive, and automated personal healthcare assistant. This technology will be validated in patients who have chronic heart failure (HF). Half of the study patients will receive an Amazon Echo Dot (Alexa) enhanced with a HF Care custom Alexa Skill that is patient-specific, or Alexa+. Data on patient interactions with the device will be followed for three months. The control groups will receive standard of care (SOC) HF management. Both study and control groups will receive regular follow up from the HF nurse and data from all hospital or clinic visits will be captured from the EHR.
Investigators
Nawar Shara
Director, Department of Biostatistics and Biomedical Informatics
Medstar Health Research Institute
Eligibility Criteria
Inclusion Criteria
- •Heart failure patients seen at the MedStar heart failure clinic and the MedStar Washington Hospital Center inpatient heart failure service
- •At least 18 years of age
- •Have access to in-home Wi-Fi
Exclusion Criteria
- •Participation in another interventional clinical trial
Outcomes
Primary Outcomes
Change in comfort level using Alexa+ technology as measured by the pre and post-test technology comfort survey
Time Frame: 3 months
Secondary Outcomes
- Change in number of hospitalizations as measured by hospitalization data extracted from the EHR(3 months)
- Change in medication adherence as measured by number of prescriptions filled extracted from the EHR(3 months)