Pilot to Assess Feasibility of Using RecoverLINK Technology to Supplement Outpatient Care for Heart Failure Patients
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 46
- Locations
- 1
- Primary Endpoint
- User engagement: # symptom surveys completed/30 days
Study Overview
Brief Summary
The primary objective is to examine feasibility of incorporating RecoverLINK into the standard of care as a function of (i) user engagement, (ii) user satisfaction, and (iii) workflow efficiency. As secondary objectives, the investigators will collect preliminary data to examine the association between patient engagement with the RecoverLINK app and (i) changes in patient knowledge and behavior, and (ii) hospital readmission(s) at 30, 60, and 90-day time periods post-enrollment.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Heart failure (HF) patients with a rapid follow up appointment scheduled at the Mount Sinai HF clinic
- •English-speaking
- •With either access to (i) an iOS smart device or (ii) wifi at-home
Exclusion Criteria
- •Patients meeting any of the following criteria:
- •A heart transplant
- •A mechanical circulatory support (MCS) device
- •An altered mental status
- •Serious co-morbidities (as identified by Mount Sinai team)
- •Cognitive impairments (as identified by Mount Sinai team)
- •Inability to use technology (as identified by Mount Sinai team)
Arms & Interventions
RecoverLINK technology
RecoverLINK is a two-part mHealth technology designed to supplement traditional care transitional programs for heart failure (HF) patients.
Intervention: RecoverLINK technology (Other)
Outcomes
Primary Outcomes
User engagement: # symptom surveys completed/30 days
Time Frame: 30 days
User satisfaction: Percent patients report "satisfied" via post-program survey
Time Frame: 30 days
Workflow efficiency: mean/median time to resolution of patient alerts
Time Frame: 30 days
Secondary Outcomes
- Hospital admission(30, 60, 90 days)
- Mean difference in pre/post SCHIFI score(30 days)