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NCT07800312Completed

PechaKucha Versus PowerPoint for Parkinson's Disease Education in Nurses

PechaKucha Versus PowerPoint in Nursing Education: A Quasi-Experimental Study

Source: ClinicalTrials.gov · Last updated 2 Sept 2026

Brief summary (registry, in English)

This study compared the effects of PechaKucha and traditional PowerPoint presentation techniques used for Parkinson's disease education on nurses' knowledge and awareness levels. The study used a two-group pretest-posttest quasi-experimental design. A total of 72 nurses were assigned to the PechaKucha intervention group (n=36) or the PowerPoint control group (n=36) using 1:1 block randomization. Both groups received Parkinson's disease education with identical educational content and learning objectives. The PechaKucha presentation consisted of 20 slides automatically advancing every 20 seconds, whereas the PowerPoint presentation was delivered using a conventional flexible-paced format. Parkinson's disease knowledge and awareness were assessed before and immediately after the educational intervention. The study aimed to determine whether the presentation technique influenced nurses' knowledge and awareness following Parkinson's disease education.

Status (registry)
Completed
Study type
Interventional
Enrollment
72 (actual)
First submitted
29 Aug 2026
Start date
2 Jan 2026
Primary completion date
14 Feb 2026
Lead sponsor
Istanbul University - Cerrahpasa
NCT number
NCT07800312

What you commit to

  • Study type: Interventional
  • Participants enrolled: 72
  • From 2 Jan 2026 to the primary completion date, 14 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • None specified.

Who the study is looking for

  • Appointed to the study hospital within the previous 12 months. Actively working as a nurse at the time of the study. Voluntarily agreed to participate in the study and provided written informed consent.

Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sultan Abdulhamid Han Training and Research Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.