NCT07736326

Brief Summary

The research was conducted between January 2025 and May 2025 using a randomized controlled experimental design with a pre-test-post-test pproach. A total of 76 nurses working at a state university hospital in Istanbul participated in the study. The experimental group received training through the Pecha-Kucha method, while the control group received traditional instruction. Data were collected using the Individual Characteristics Form, the Nurses' Knowledge Assessment Form for Anticoagulant Drug Administration, the Skill Assessment Form for Anticoagulant Drug Administration, and the Visual Analog Scale.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
76

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

January 2, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2025

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

July 2, 2026

Completed
28 days until next milestone

First Posted

Study publicly available on registry

July 30, 2026

Completed
Last Updated

July 30, 2026

Status Verified

January 1, 2025

Enrollment Period

5 months

First QC Date

July 2, 2026

Last Update Submit

July 25, 2026

Conditions

Keywords

nurse trainingmedication safety

Outcome Measures

Primary Outcomes (2)

  • "Anticoagulant Drug Administration Knowledge Level Assessment Form"

    After training Day 1

  • Anticoagulant Drug Administration Skills Assessment Form

    after training Day 1

Secondary Outcomes (1)

  • Visual Analog Scale for Satisfaction

    after training Day 1

Study Arms (2)

Conventional

NO INTERVENTION

The training was conducted with 38 nurses who met the traditional presentation training research criteria. The training was completed in separate sessions of 8-10 nurses. Groups were planned considering the nurses' working days and hours. The researcher provided 25-30 minutes of "Anticoagulant Drug Administration" training using a PowerPoint presentation prepared in accordance with current literature and delivered face-to-face.

Pecha-Kucha

EXPERIMENTAL

The presentation, conducted by the researcher using the Pecha-Kucha method in accordance with current literature, consisted of 20 slides with minimal text and a high concentration of visuals related to anticoagulant drugs, each slide presented for 20 seconds, totaling 6 minutes and 40 seconds. The instructor was positioned to be more active and the center of attention.

Other: Pecha-Kucha

Interventions

The presentation, conducted by the researcher using the Pecha-Kucha method in accordance with current literature, consisted of 20 slides with minimal text and a high concentration of visuals related to anticoagulant drugs, each slide presented for 20 seconds, totaling 6 minutes and 40 seconds. The instructor was positioned to be more active and the center of attention.

Pecha-Kucha

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • volunteered to participate
  • administered anticoagulant medication in their clinic.

You may not qualify if:

  • Non-volunteered to participate

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Health Sciences

Üsküdar, Istanbul, 34, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assoc. Prof.

Study Record Dates

First Submitted

July 2, 2026

First Posted

July 30, 2026

Study Start

January 2, 2025

Primary Completion

May 31, 2025

Study Completion

May 31, 2025

Last Updated

July 30, 2026

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will share

all IPD that underlie results in a publication

Locations