Study Stopped
Per PI this QI/QA resident project was not initiated. Record should be deleted.
Impact of Video Discharge Instructions on Heart Failure Patient's Knowledge
VID-HF
Heart Failure Patient Education Using Video and Paper Discharge Instructions
1 other identifier
interventional
N/A
1 country
1
Brief Summary
With improve care of patients with heart failure, many patients are living longer. Care for these patients is now not only focused on mortality but also on the quality of life. Patient knowledge about heart failure and their overall compliance with the necessary lifestyle changes will lead to an improved quality of life. Discovering alternative ways to improve patient knowledge is key to long term survival. This studies objective is to assess the overall impact of video discharge instructions as compared to paper discharge instructions on Heart Failure Knowledge among an under-served patient population.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started May 2018
Shorter than P25 for not_applicable heart-failure
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 12, 2018
CompletedStudy Start
First participant enrolled
May 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 7, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
August 7, 2018
CompletedFirst Posted
Study publicly available on registry
June 18, 2023
CompletedJune 18, 2023
June 1, 2023
2 months
January 12, 2018
June 13, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Heart Failure Knowledge Score
Participants knowledge about heart failure will be assessed using the validated Atlanta Heart Failure Knowledge Test(AHFKT- V3). This is a test which includes 30 questions with a minimum score of 0 and a maximum score of 30. Each Participant will take the test and will subsequently be given either paper discharge instructions or both video and paper discharge instructions. After reading and/or watching the discharge instructions, each participant will take the same test once again. The difference in the pre and post intervention scores will be calculated and the investigators will assess if there is a significant difference in the mean change in score the control(Paper) vs. Intervention groups(Video).
1hr
Secondary Outcomes (3)
Participant Satisfaction with discharge Instructions
1 day
Post hospital followup rates
30 days
Heart Failure Readmission rates
30days
Study Arms (2)
Paper Discharge Instruction
NO INTERVENTIONPatient will be given paper discharge instructions
Video Discharge Instructions
EXPERIMENTALPatient will be given Video discharge instructions
Interventions
Patient will watch a video discharge instructions in addition to the standard paper instructions. They will also take the pre and post test as the control group
Eligibility Criteria
You may qualify if:
- hospital admission with a diagnosis of Heart Failure (HF)- Heart failure with reduced ejection fraction or heart failure with preserved Ejection fraction
- planned discharge from hospital to home setting
- able to read and write English
- Acceptable to answer Questionnaire and to receive a call at the end of the study
You may not qualify if:
- Planned discharge to long term acute care
- Patients with unstable housing
- imprisoned patients
- patients who are pregnant
- illiteracy (defined as inability to write or read) and non-native speakers of English
- impaired cognition
- impaired vision
- Patients with End Stage Renal Disease(ESRD)
- Cancer patients
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Yasmeen Golzarlead
Study Sites (1)
John H Stroger Hospital
Chicago, Illinois, 60612, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 12, 2018
First Posted
June 18, 2023
Study Start
May 1, 2018
Primary Completion
July 7, 2018
Study Completion
August 7, 2018
Last Updated
June 18, 2023
Record last verified: 2023-06