NCT06297382

Brief Summary

The goal of this randomized controlled study is to determine the impact of ChatGPT based nursing process training on nursing students' clinical decision-making competencies and artificial intelligence anxiety. Population and Sample: The population of the research consists of senior students studying at Gülhane Faculty of Nursing, University of Health Sciences. Power analysis was performed to determine the number of people to be included in the study. The power of the test was calculated with the G\*Power 3.1 program. In a similar study in the relevant literature, the effect size regarding the change in clinical decision-making level was calculated as 0.898. In order to exceed the 99% value in determining the power of the study; At the 5% significance level and 0.898 effect size, 44 people, 22 people in the groups, need to be reached (df=21; t=1.721). In the research, it was aimed to reach a total of 60 people, 30 people in the groups, considering the high power of the test and the losses.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2024

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

First Submitted

Initial submission to the registry

February 29, 2024

Completed
6 days until next milestone

Study Start

First participant enrolled

March 6, 2024

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 7, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 24, 2024

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 14, 2024

Completed
Last Updated

August 16, 2024

Status Verified

August 1, 2024

Enrollment Period

2 months

First QC Date

February 29, 2024

Last Update Submit

August 14, 2024

Conditions

Keywords

Artificial IntelligenceStudents, Nursing

Outcome Measures

Primary Outcomes (3)

  • Descriptive Information Form

    It was prepared by the researchers and consists of 6 questions regarding demographic characteristics and the use of artificial intelligence.

    6 weeks

  • Clinical Decision Making Scale in Nursing

    The scale, which was developed to measure the clinical decision-making perceptions of nursing students based on their self-expression, was adapted into Turkish. The scale, which consists of four sub-dimensions, has 40 items. Sub-dimensions; It is stated as searching for options, declaring goals and values, evaluating and re-evaluating the results, searching for information and impartial assimilation of new information. Each subscale consists of 10 items. In the scale, 18 negative items are scored reversely. The five-point Likert type scale is scored as "Always-5, Frequently-4, Sometimes-3, Rarely-2 and Never-1" and the lowest and highest values are 40-200 for the total score of the scale and 40-200 for each sub-dimension. It varies between 10-50. High scores from the scale indicate that the perception of decision-making is high, while low scores indicate that the perception of decision-making is low.

    6 weeks

  • Artificial Intelligence Anxiety Scale:

    Artificial Intelligence Anxiety Scale developed by Wang and Wang (2019) was adapted into Turkish by Akkaya et al (2021). The Turkish form of YZKS consists of 16 items and 4 dimensions and is a 5-point Likert type scale. The sub-dimensions are learning, job switching, sociotechnical blindness and artificial intelligence configuration.

    6 weeks

Study Arms (2)

Experimental

EXPERIMENTAL

In the 2023-2024 academic year, those in the experimental group will be determined by randomization among the students who are senior students at the faculty of nursing, who have not received ChatGPT training before and who agree to participate in the research. Students in the experimental group will have data collection forms filled out. Then, 4 hours of ChatGPT based nursing process training will be given. Measurements will be taken again after the training and 6 weeks after the training.

Behavioral: ChatGPT Based Nursing Process Training

Control

NO INTERVENTION

In the 2023-2024 academic year, students who are senior students at the faculty of nursing, who have not received ChatGPT training before and who agree to participate in the research, will be determined by randomization and those in the control group will be determined. Students in the control group will fill out data collection forms. Students in the control group will not be given any training. Data collection forms will be applied again 6 weeks after the training.

Interventions

ChatGPT Based Nursing Process Training topics: Lesson 1: Use of artificial intelligence and ChatGPT in healthcare Lesson 2: Using ChatGPT in determining nursing diagnoses and goals Lesson 3: Using ChatGPT to determine nursing interventions Lesson 4: Things to consider and ethical principles when using ChatGPT when creating a nursing process.

Experimental

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Being a senior student at the faculty of nursing in the 2023-2024 academic year
  • Agreeing to participate in the research

You may not qualify if:

  • Having previously received ChatGPT training
  • Withdrawing from the research voluntarily
  • Incompletely filled forms

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Miray AKSU

Ankara, Çankaya, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
Experimental and control groups will be determined using https:// www.randomizer.org.
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: This research will be conducted as an experimental study with pretest-posttest randomised control group design.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assist. Prof.

Study Record Dates

First Submitted

February 29, 2024

First Posted

March 7, 2024

Study Start

March 6, 2024

Primary Completion

April 24, 2024

Study Completion

August 14, 2024

Last Updated

August 16, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations