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OpenTrials
Completed

NCT Number: NCT05189340

Development of Discharge Education Video for Solid Organ Transplant Recipients

Audiovisual teaching aids can play a significant role for the retention of new material and help overcome barriers such as the physical presence or time restrictions of an instructor. In a clinical setting, multimedia health education can offer an advantage over traditional didactic teaching by engaging patients through visual content and unlimited accessibility.

A critical factor to long-term survival of solid organ transplant recipients is compliance to post-transplantation medication and follow-up patient care. Transplant pharmacists serve on multidisciplinary care teams as the medication experts that provide discharge education to recipients and caregivers often at the bedside. The adoption of digital multimedia content for patient education can increase engagement of diverse learning styles while simultaneously reducing potential time conflicts in hospital practice. This study contributes to the literature by assessing the effectiveness of discharge education video(s) on patient satisfaction and knowledge levels which are currently limited.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Johns Hopkins Hospital

Baltimore, Maryland, 21287, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who are solid organ transplant recipients at Johns Hopkins Hospital
  • Patients who are being managed by an adult solid-organ transplant surgical service
  • Patients who can speak and read the English language

Exclusion criteria

  • Patients with language access services needs will be excluded
  • Patients who do not meet inclusion criteria

Treatment and study plan

Educational videos

Other

Series of six videos each covering a specific aspect of post-transplant care related to medication use or monitoring

Primary outcomes

  1. Patient Transplant Medication and Care Knowledge

    Time frame: Pre- and post-education; pre-education assessment will be completed as soon as feasible after transplant (estimate 1-3 days) and consent; post-education assessment will be completed as soon as is feasible after initial education (estimate 0-2 days)

    Change in performance pre and post-education based on responses to questionnaire

  2. Patient Satisfaction with Educational Method

    Time frame: As soon as feasible post-education, in concert with post-education knowledge assessment (estimate 0-2 days)

    Difference in satisfaction as determined by response to questionnaire post education. A single question score from 1 to 10 will be used, with 10 being highest satisfaction and 1 being the lowest level of satisfaction

Secondary outcomes

  1. Pharmacist Time Requirement

    Time frame: As soon as feasible post-education (estimate 0-2 days)

    Time required by pharmacist for education

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Registry information

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jan 12, 2022
Registry last updated
Jun 8, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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