Teaching Family Planning Skills With Standardized Patients"

July 10, 2024 updated by: İlknur Atasever, Suleyman Demirel University

Suleyman Demirel University

The research is planned to be carried out in the Simulated Patient Laboratory of Süleyman Demirel University Faculty of Medicine. The population of the research will consist of students taking the Hem 327 Women's Health and Diseases Nursing course in the fall semester of the 2023-2024 academic year (N: 179). Students receive training in small groups of 30-40 people in the professional skills laboratory. It is planned to study with a total of 80 students, 40 in the intervention group and 40 in the control group. Students will be assigned to intervention and control groups by lottery. The entire intervention and control group will receive theoretical training on "Family Planning", which is included in the 327 Women's Health and Diseases Nursing course. The course, conducted by the research faculty member using lecture, question-answer and discussion methods, will last three hours. Students participating in the study during the week of the theoretical course will be asked to fill out the Introductory Characteristics Form and the Family Planning Counseling Information Form.

Study Overview

Detailed Description

The main purpose of nursing education is; To train healthcare professionals who can combine theoretical knowledge with practice, and who have acquired critical thinking and effective problem-solving skills. Clinical practice is one of the most important elements of nursing teaching. It is thought that simulation training will be effective in preparing students for clinical practice and will increase their self-confidence in clinical practice by improving their clinical decision-making and application skills. Therefore, whether knowledge and skill gains can be transferred to nursing practice is an important area of interest in simulation research. The research is planned to be carried out in the Simulated Patient Laboratory of Süleyman Demirel University Faculty of Medicine. The population of the research will consist of students taking the Hem 327 Women's Health and Diseases Nursing course in the fall semester of the 2023-2024 academic year (N: 179). Students receive training in small groups of 30-40 people in the professional skills laboratory. It is planned to study with a total of 80 students, 40 in the intervention group and 40 in the control group. Students will be assigned to intervention and control groups by lottery. The entire intervention and control group will receive theoretical training on "Family Planning", which is included in the 327 Women's Health and Diseases Nursing course. The course, conducted by the research faculty member using lecture, question-answer and discussion methods, will last three hours. Students participating in the study during the week of the theoretical course will be asked to fill out the Introductory Characteristics Form and the Family Planning Counseling Information Form. In the same week, students in the control group will practice family planning education skills in the vocational skills laboratory. At the end of the application, students will fill out the Effective Communication Skills Evaluation Form and the Family Planning Education Skills Evaluation Form. Students in the intervention group are; They will participate in standard patient education that includes a family planning counseling scenario. Students will be given preliminary information before encountering a standard patient. During standard patient preparations; standard patients will be informed about the scenarios. Standard clothes and additional materials that patients will use while performing the scenario will be provided. Care will be taken to ensure that individuals serving as standard patients have previously taken part in other studies as standard patients. Then, the student will be brought together with the standard patient in the standard patient room of the clinical simulation training laboratory and a video recording will be taken at this time. The standard patient will behave in accordance with the patient role in the scenario given to him by the researcher. The application recording will be monitored by the researcher and the observer in the observation room in the standard patient room, and the Effective Communication Skills Evaluation Form and Family Planning Education Skill Evaluation Form will be filled in to evaluate the skill levels of the students. Then, a debriefing session will be held in the debriefing room, in line with the debriefing questions. Meanwhile, students will be given feedback on their deficiencies and performance in the application. Students' satisfaction and self-confidence towards this education will be evaluated with the Student Satisfaction and Self-Confidence Scale in Learning. The evaluation of the data will be done on a computer using the SPSS (Statistical Package For Social Sciences) 21.0 package program. In the analysis of data, percentage distributions, mean, standard deviation, chi-square test, and t-test in dependent groups will be used. Research findings will be evaluated at a 95% confidence interval and a significance level of p<0.05. In order to conduct the research, ethics committee approval was obtained from the Süleyman Demirel University Ethics Committee Presidency and legal permission was obtained from the Dean's Office of Süleyman Demirel University Faculty of Medicine, where the research will be conducted.

Study Type

Interventional

Enrollment (Actual)

80

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Çünür
      • Isparta, Çünür, Turkey, 32260
        • Suleyman Demirel University Health Sciences Faculty Nursing Department

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

- To be a third-year nursing student at the Faculty of Health Sciences

• To consent to participate in the research.

Exclusion Criteria:

  • Not completing any stage of the study
  • Requesting to withdraw from the study
  • Having previously taken the Obstetrics and Gynecology Nursing course

Study Plan

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

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Classical Training
In the professional skills laboratory, students in the control group will practice family planning education skills
Students in the education group will practice family planning education skills in the professional skills laboratory.
Other: Standard Patient Interviews
Students in the standard patient education group will receive standard patient education including a family planning counseling scenario.
Students in the standardized patient education group will receive training involving a family planning counseling scenario with standardized patients.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Standard patient practice has an impact on students' satisfaction level.
Time Frame: through study completion, an average of 6 month
Student Satisfaction and Confidence Scale in Learning
through study completion, an average of 6 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The effect of standardized patient practice on students' self-confidence has been investigated
Time Frame: through study completion, an average of 6 month
Family Planning Counseling Information Form, Effective Communication Form,Family Planning Education Skills Assessment Form
through study completion, an average of 6 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ilknur Atasever, Assist. Prof., Suleyman Demirel University
  • Principal Investigator: Ilknur Atasever, Assist. Prof.., Suleyman Demirel University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 31, 2024

Primary Completion (Actual)

June 5, 2024

Study Completion (Actual)

June 5, 2024

Study Registration Dates

First Submitted

May 23, 2024

First Submitted That Met QC Criteria

July 10, 2024

First Posted (Actual)

July 12, 2024

Study Record Updates

Last Update Posted (Actual)

July 12, 2024

Last Update Submitted That Met QC Criteria

July 10, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • u3mjm2ey

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Our plan aims to ensure transparent sharing of research results and accessibility to the scientific community. Individual participant data will be safeguarded in accordance with privacy standards.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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