Impact of Video Discharge Instructions on Heart Failure Patient's Knowledge

Heart Failure Clinical Trial

— VID-HF  

Official title:

Heart Failure Patient Education Using Video and Paper Discharge Instructions

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT05908617
• Other study ID #: 17-538-Stroger
• Status: Withdrawn
• Phase: N/A
• Start date: May 1, 2018
• Est. completion date: August 7, 2018

Study information

• Verified date: June 2023
• Source: Cook County Health
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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: 1. Medial history of the patient 2. Educational background 3. Social Status 4. Patients Health Measurement: Self Efficacy for managing medications and Treatment Management, Informational Support

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: August 7, 2018
• Est. primary completion date: July 7, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Heart Failure

Intervention

Other:
• Video Discharge
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

Locations

Country	Name	City	State
United States	John H Stroger Hospital	Chicago	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
Yasmeen Golzar

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	Participant Satisfaction with discharge Instructions	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
Secondary	Post hospital followup rates	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
Secondary	Heart Failure Readmission rates	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