The Effect of Preoperative Education Delivered Using the Pecha Kucha Method on the Quality of Recovery
1 other identifier
interventional
61
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 9, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 2, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 2, 2026
CompletedFirst Submitted
Initial submission to the registry
January 22, 2026
CompletedFirst Posted
Study publicly available on registry
February 3, 2026
CompletedFebruary 3, 2026
February 1, 2026
7 months
January 22, 2026
February 2, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Quality of Recovery-15 (QoR-15)
The original scale was developed by Myles et al. (2000) to assess postoperative recovery quality¹⁷, and a shortened 15-item version was later developed by Stark et al.¹⁸. The Turkish validity and reliability study was conducted by Kara et al. in 2022. The scale consists of five subdimensions: pain, physical comfort, physical independence, psychological support, and emotional state. Each item is scored on a scale from 0 to 10, with total scores ranging from 0 to 150. Scores between 136-150 indicate excellent recovery, 122-135 good recovery, 90-121 moderate recovery, and 0-89 poor recovery¹⁹.
the morning of the surgery day, 24 hours after the surgery
Study Arms (2)
Control Group
NO INTERVENTIONAfter obtaining the necessary approvals, participants were randomly assigned to either the intervention group or the control group 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.
Study Group
EXPERIMENTALAfter 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
Interventions
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.
Eligibility Criteria
You may qualify if:
- The study sample consisted of patients who agreed to participate and were scheduled for cataract surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara Yıldırım Beyazıt University
Ankara, Ankara, 06010, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 22, 2026
First Posted
February 3, 2026
Study Start
May 9, 2025
Primary Completion
December 2, 2025
Study Completion
January 2, 2026
Last Updated
February 3, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
I don't want to share it until it's published.