Clinical Trials in Germany / NCT06652919
Recruiting
Observational
Survey on the Evaluation of Medication Information Leaflets for Organ Transplant Patients
NCT06652919 · tracked via the Priya Life Science Germany tracker
Condition(s) studied
Organ Transplantation
Study summary
The aim of this study is to collect feedback from organ transplant patients or their caregivers/relatives on the medication information leaflets we've developed, using a questionnaire, and to adjust the content to better meet the specific needs of this unique patient group.
Eligibility
Inclusion Criteria:
* Patients who have undergone solid organ transplantation (kidney, liver, heart, lung)
* Caregivers or family members of organ transplant patients
* German-speaking individuals
* adult
Exclusion Criteria:
* Individuals who are not able to provide consent
* Non-German-speaking individuals
* under 18 years old
* Patients who have undergone organ transplantation and are no longer taking immunosuppressants
Primary outcome measure(s)
- Consumer Information Rating Form (CIRF): Mean "comprehensibility" score, mean "future use" score, mean "utility" score and mean "design quality" score. — 3 months
In this research, the measurement instrument called the Consumer Information Rating Form (CIRF) is used, though the content has been slightly adapted to fit our study. It was developed as a direct method for quantifying consumers' perceptions of written patient information, including their views on its comprehensibility, utility, and overall design quality. In the questionnaire, four perspectives will be evaluated using Likert scales, including "comprehensibility" (5 items, with a total score range from 5 to 25), "future use" (3 items, with a total score range from 3 to 15), "utility" (5 topics with two perspectives: the amount of information provided and its usefulness, with a total score range from 3 to 20.), and "design quality" (6 items, with a total score range from 6 to 30). Higher scores indicate better quality of the patient information leaflet. - Participants' characteristics — 3 months
Gender, age group, highest level of education, current employment status, if participant has worked in the healthcare system, Which patient information leaflet did the participant evaluate? What type of organ transplant has the participant or the person they look after received? (Kidney, liver, heart, or lung transplant), How long has it been since the transplant?
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Institute of Pharmaceutical and Medicinal Chemistry, Clinical Pharmacy, University of Münster | Münster | North Rhine-Westphalia | Recruiting |
More Universität Münster trials in Germany
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06652919 on ClinicalTrials.gov ↗ ← All trials in Germany