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Clinical Trials/NCT04219839
NCT04219839CompletedNot Applicable

Duke Transplant University: A Digital Patient Education Portal

Duke University2 sites in 1 country83 target enrollmentStarted: November 23, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
83
Locations
2
Primary Endpoint
Change in patient transplant knowledge during intervention as measured by the scores from the "Transplant Knowledge" block within the Duke Transplant University Assessment

Study Overview

Brief Summary

The purpose of this research study is to determine the effectiveness of educational videos for patients who have just had kidney transplant compared to usual patient education practices. Eligible patients will have the opportunity to enroll in this study after their transplant procedure either before hospital discharge or at their first follow up clinic visit.

Detailed Description

Participants will then complete a demographic survey and knowledge assesment to establish their baseline of knowledge regarding post-transplant care, medication adherence and patient satisfaction. Participants will then be randomly selected to receive either the usual patient education care provided for patients following kidney transplant, or to receive the usual care plus access to educational videos designed especially for post- transplant patients. Videos can be viewed on a tablet computer with their transplant team during clinic visits and at home using a smartphone.

At 3 months post-transplant, all participants will be asked to repeat the knowledge assessment. Hospital re-admissions and patient satisfaction will be measured at 6 months after transplant.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • recent kidney transplant recipients
  • competent with the capacity to give legal written consent

Exclusion Criteria

  • Unable to sign informed consent.
  • Patients with delirium, dementia, or other cognitive impairment that would not allow informed consent to enter the study.
  • patients with severe vision or auditory impairment who are unable to view or hear electronic videos at close range.
  • patients who are unable to understand the English language.

Outcomes

Primary Outcomes

Change in patient transplant knowledge during intervention as measured by the scores from the "Transplant Knowledge" block within the Duke Transplant University Assessment

Time Frame: Baseline to 3 months

Change will be measured by comparing the scores from the Transplant Knowledge assessments completed at baseline and 3 months.

Number of medication errors made post-transplant as measured by pillbox errors

Time Frame: 1 month, 2 months and 3 months

The number of medication errors will be measured by counting number of pill box errors identified by pharmacist's review of patient's pillbox during transplant follow up clinic visits conducted at 1 month, 2 months and 3 months.

Change in perceptions of self-efficacy as measured by the scores from the "Self-Efficacy and Resiliency" assessment within the Duke Transplant University Assessment

Time Frame: Baseline to 3 months

Change will be measured by comparing the scores from the Self-Efficacy and Resiliency assessments completed at baseline and 3 months.

Secondary Outcomes

  • Patients' satisfaction with the transplant experience as measured by satisfaction ratings(Baseline and 6 months)
  • Number of hospital re-admissions post transplant(Baseline to 6 months)

Investigators

Sponsor
Duke University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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