NCT06499558

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2024

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 23, 2024

Completed
8 days until next milestone

Study Start

First participant enrolled

May 31, 2024

Completed
5 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 5, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 5, 2024

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 12, 2024

Completed
Last Updated

July 12, 2024

Status Verified

July 1, 2024

Enrollment Period

5 days

First QC Date

May 23, 2024

Last Update Submit

July 10, 2024

Conditions

Keywords

educationfamily planningstandard patient

Outcome Measures

Primary Outcomes (1)

  • Standard patient practice has an impact on students' satisfaction level.

    Student Satisfaction and Confidence Scale in Learning

    through study completion, an average of 6 month

Secondary Outcomes (1)

  • The effect of standardized patient practice on students' self-confidence has been investigated

    through study completion, an average of 6 month

Study Arms (2)

Classical Training

OTHER

In the professional skills laboratory, students in the control group will practice family planning education skills

Other: Classical Training

Standard Patient Interviews

OTHER

Students in the standard patient education group will receive standard patient education including a family planning counseling scenario.

Other: Standard Patient Interviews

Interventions

Students in the education group will practice family planning education skills in the professional skills laboratory.

Classical Training

Students in the standardized patient education group will receive training involving a family planning counseling scenario with standardized patients.

Standard Patient Interviews

Eligibility Criteria

Age21 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • \- To be a third-year nursing student at the Faculty of Health Sciences
  • To consent to participate in the research.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Suleyman Demirel University Health Sciences Faculty Nursing Department

Isparta, Çünür, 32260, Turkey (Türkiye)

Location

Study Officials

  • Ilknur Atasever, Assist. Prof.

    Suleyman Demirel University

    PRINCIPAL INVESTIGATOR
  • Ilknur Atasever, Assist. Prof..

    Suleyman Demirel University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
In the study, participants are divided into two groups: the laboratory training group (the group receiving standard training) and the group receiving standard patient training. For this reason, blinding was not possible among the participants.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: In the study, participants are divided into two groups: the laboratory training group (the group receiving standard training) and the group receiving standard patient training.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

May 23, 2024

First Posted

July 12, 2024

Study Start

May 31, 2024

Primary Completion

June 5, 2024

Study Completion

June 5, 2024

Last Updated

July 12, 2024

Record last verified: 2024-07

Data Sharing

IPD Sharing
Will not share

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.

Locations