VID-HF: Impact of Video Discharge Instructions on Heart Failure Patient's Knowledge

Sponsor
Yasmeen Golzar (Other)
Overall Status
Withdrawn
CT.gov ID
NCT05908617
Collaborator
(none)
0
1
2
3.2
0

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Video Discharge
N/A

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:
  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

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Heart Failure Patient Education Using Video and Paper Discharge Instructions
Actual Study Start Date :
May 1, 2018
Actual Primary Completion Date :
Jul 7, 2018
Actual Study Completion Date :
Aug 7, 2018

Arms and Interventions

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

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

Outcome Measures

Primary Outcome Measures

  1. Change in Heart Failure Knowledge Score [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).

Secondary Outcome Measures

  1. Participant Satisfaction with discharge Instructions [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

  2. Post hospital followup rates [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.

  3. Heart Failure Readmission rates [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 John H Stroger Hospital Chicago Illinois United States 60612

Sponsors and Collaborators

  • Yasmeen Golzar

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yasmeen Golzar, Principal Investigator, Cook County Health
ClinicalTrials.gov Identifier:
NCT05908617
Other Study ID Numbers:
  • 17-538-Stroger
First Posted:
Jun 18, 2023
Last Update Posted:
Jun 18, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Yasmeen Golzar, Principal Investigator, Cook County Health
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 18, 2023