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The Effect of Preoperative Education Delivered Using the Pecha Kucha Method on the Quality of Recovery

NCT07383168 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2026-02-03

No results posted yet for this study

Summary

Objective: The aim of this research is to determine the effect of the Pecha Kucha training method on the quality of patient recovery in patient education.

Methods: This study was conducted at the ophthalmology clinic of a training and research hospital in Türkiye. A total of 61 patients scheduled for cataract surgery were randomly assigned to either the intervention group (n = 31) or the control group (n = 30). The study group received preoperative education using the Pecha Kucha method. Data were collected face-to-face using a sociodemographic data form and the Quality of Healing-15 (QoR-15) questionnaire. Data were analyzed using descriptive statistics and appropriate parametric and non-parametric tests, with a statistical significance level of p \< 0.05.

Conditions

  • Cataract
  • Education of Patients
  • Postoperative Recovery

Interventions

OTHER

Education with Pecha Kucha

After obtaining the necessary approvals, participants were randomly assigned to either the intervention group (n = 31) or the control group (n = 30) using randomization. On the morning of surgery, both groups completed the sociodemographic data form and the QoR-15 questionnaire through face-to-face interviews conducted by the researchers. Following data collection, patients in the intervention group received preoperative education using the Pecha Kucha technique. This education consisted of a 6-minute and 40-second presentation delivered via a smartphone, comprising 20 slides with intensive visual content and minimal text.

Sponsors & Collaborators

  • Ankara Yildirim Beyazıt University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-05-09
Primary Completion
2025-12-02
Completion
2026-01-02

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 NCT07383168 on ClinicalTrials.gov