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PechaKucha Versus PowerPoint for Parkinson's Disease Education in Nurses

NCT07800312 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2026-09-02

No results posted yet for this study

Summary

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.

Conditions

  • Nursing Education

Interventions

OTHER

PechaKucha-Based Parkinson's Disease Education

Participants received Parkinson's disease education using the PechaKucha presentation technique. The presentation consisted of 20 slides that automatically advanced every 20 seconds, resulting in a total presentation duration of 6 minutes and 40 seconds.

OTHER

PowerPoint-Based Parkinson's Disease Education

Participants received Parkinson's disease education using a traditional PowerPoint presentation. The presentation consisted of 23 slides, was delivered with flexible pacing, and lasted approximately 30-35 minutes. The educational content and learning objectives were identical to those used in the PechaKucha group.

Sponsors & Collaborators

  • Istanbul University - Cerrahpasa

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-01-02
Primary Completion
2026-02-14
Completion
2026-04-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07800312 on ClinicalTrials.gov