Completed

Determining the Effects of an Evidence-Based Practice Education Intervention Program Applied to Nursing Students: A Randomized Controlled Trial

What is being tested

Evidence-Based Education intervention

Other

Who is being recruted

From 18 to 32 Years

+4 Eligibility Criteria

See all eligibility criteria

How is the trial designed

Supportive Care Study

Interventional

Study Start: February 2022

See protocol details

Summary

Principal SponsorSelcuk University

Last updated: January 28, 2026

Sourced from a government-validated database.Claim as a partner

Study start date: February 12, 2022

Actual date on which the first participant was enrolled.

This study aims to explore how an educational program about Evidence-Based Practice (EBP) affects nursing students. The program is designed to help students better understand and apply research findings in their practice. Nursing students are targeted because effective EBP can enhance patient care and outcomes. The goal is to see if this educational intervention improves students' knowledge, attitudes, and behaviors related to evidence-based nursing. Participants in the study are divided into two groups. One group receives 12 hours of training on EBP over seven sessions, while the other group does not receive any special training. To measure the impact of the training, students fill out surveys that assess their knowledge and attitudes toward evidence-based practices before and after the sessions. Researchers use statistical tests to compare the results between the two groups and determine if the educational program makes a significant difference in the students' understanding of EBP.

Official TitleDetermining the Effects of an Evidence-Based Practice Education Intervention Program Applied to Nursing Students: A Randomized Controlled Trial

NCT06195397

Principal SponsorSelcuk University

Last updated: January 28, 2026

Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

108 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.

Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 32 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

2 inclusion criteria required to participate

Be registered in the third year of nursing

Having taken a research course

2 exclusion criteria prevent from participating

The student suspends his/her registration or transfers to another university

Not volunteering to participate in the study

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.

Treatment Groups

Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group

Treatment Groups

Group I

Experimental

A total of 12 hours of Evidence-Based Education intervention was applied to students in the intervention group, spread over 7 sessions.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

Suspended

Selcuk University

Konya, Turkey (Türkiye)Open Selcuk University in Google Maps

Suspended

Selcuk University

Konya, Turkey (Türkiye)

Completed2 Study Centers