- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05908617
Impact of Video Discharge Instructions on Heart Failure Patient's Knowledge (VID-HF)
Heart Failure Patient Education Using Video and Paper Discharge Instructions
Study Overview
Detailed Description
In this study, we will randomized patients admitted to the hospital with heart failure exacerbation to receive either paper or video discharge instructions within a day prior to discharge. The video and paper instructions will have the same content. The patients will take a pre-test and post-test and the change in scores among the patients who received the video and paper discharge instructions will be compared. Other points of interest include participant satisfactions with discharge instruction, followup at post hospital appointment and 30-day readmission.
Data to be collected includes:
- Medial history of the patient
- Educational background
- Social Status
- Patients Health Measurement: Self Efficacy for managing medications and Treatment Management, Informational Support
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Illinois
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Chicago, Illinois, United States, 60612
- John H Stroger Hospital
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Paper Discharge Instruction
Patient will be given paper discharge instructions
|
|
|
Experimental: Video Discharge Instructions
Patient will be given Video discharge instructions
|
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
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Heart Failure Knowledge Score
Time Frame: 1hr
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Participant Satisfaction with discharge Instructions
Time Frame: 1 day
|
Participant overall satisfaction with their discharge instructions will be assess using a 5 point likert scale which ranges from not at all helpful to extremely helpful
|
1 day
|
|
Post hospital followup rates
Time Frame: 30 days
|
Upon discharge from the hospital, Each participant is given a post hospital appointment within 14 days of the discharge date.
We will assess the percentage of participates in both groups who come to post hospital appointments.
|
30 days
|
|
Heart Failure Readmission rates
Time Frame: 30days
|
Investigators will assess the percentage of participants in both groups who will be readmitted to the hospital within 30days after being discharged from the index visit.
|
30days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17-538-Stroger
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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