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| ID | Type | Description | Link |
|---|---|---|---|
| K12HS019461 | U.S. AHRQ Grant/Contract | View source |
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Patient enrollment was initially suspended due to COVID19 pandemic, then the study was closed due to institutional requirements for clinical trials.
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| Name | Class |
|---|---|
| Agency for Healthcare Research and Quality (AHRQ) | FED |
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This is a patient-centered comparative effectiveness feasibility pilot designed to examine an intervention to increase heart failure self-care and symptom recognition. The investigators will randomize 100 participants to receive either usual care at the time of discharge after heart failure admission or a smartphone application that enhances self-care.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Usual care | Active Comparator | Consists of routine care at the time of hospital discharge, to be provided at the discretion of the clinicians caring for the participant. |
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| Application | Experimental | Participants will be provided a special link to navigate to the online content and resources. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Mobile Health Technology Platform | Other | When the participant navigates to the program, s/he will follow the directions on how to use the program, sign the terms of agreement, put in a password and begin the welcome page. The participant will receive daily prompts to complete brief questionnaires and review specialized content. |
| Measure | Description | Time Frame |
|---|---|---|
| Percent of participants readmitted within 30 days | 30-day readmission rate as determined by participant report or medical record query | 30 days post index discharge |
| Percent of participants readmitted within 90 days | 90-day readmission rate as determined by participant report or medical record query | 90 days post index discharge |
| Time to readmission | time to readmission | from the date of enrollment until the date of first documented admission or date of death from any cause, whichever comes first, assessed up to 90 days |
| Kansas City Cardiomyopathy Questionnaire at 30 days post enrollment | Quality of life, subjective level of function | 30 days post index discharge |
| Kansas City Cardiomyopathy Questionnaire at 90 days post enrollment | Quality of life, subjective level of function | 90 days post index discharge |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Amber E Johnson, MD | University of Pittsburgh | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Pittsburgh | Pittsburgh | Pennsylvania | 15213 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 35311679 | Derived | Johnson AE, Routh S, Taylor CN, Leopold M, Beatty K, McNamara DM, Davis EM. Developing and Implementing an mHealth Heart Failure Self-care Program to Reduce Readmissions: Randomized Controlled Trial. JMIR Cardio. 2022 Mar 21;6(1):e33286. doi: 10.2196/33286. |
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| ID | Term |
|---|---|
| D006333 | Heart Failure |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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| Usual care | Other | Routine care at the time of hospital discharge, to be provided at the discretion of the clinicians caring for the participant. |
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