Effects of Standard Patient Simulation Method in Communication With Intensive Care Patients

NCT05802823 | Unknown

• 1 other identifier: SINOPU
• Study Type: interventional
• Target: 76
• Locations: 1 country
• Sites: 1

Brief Summary

The research will be carried out in a randomized controlled experimental study design in order to evaluate the effect of standard patient simulation method on communication skills, satisfaction and self-confidence in learning of nursing students in communication with intensive care patients. The research will be conducted face-to-face with nursing students who are in the 2nd year of the Faculty of Health Sciences of Sinop University and meet the inclusion criteria in the fall semester of 2022-2023, after the necessary permissions are obtained for the study.

Conditions

Satisfaction; Communication; Confidence, Self

Keywords

simulated patient; communication; satisfaction

Outcome Measures

Primary Outcomes (1)

• Communication Evaluated Using The Therapeutic Communication Skills Scale for Nursing Students

  Scores ranging from 16 to 112 points are obtained in the scale.

  change from before implication and 3 th week of practice

Secondary Outcomes (1)

• Nurses to measure students' attitudes and beliefs about simulation using Student Satisfaction and Self-Confidence in Learning Scale

  change from before implication and 3 th week of practice

Study Arms (2)

Experimental Group

EXPERIMENTAL

Resources will be distributed to the students 1 week before the application, a scenario will be given 5 minutes before the application, and informed consent will be obtained from the students. Just before the application, information about the simulation process and analysis will be given. Students will be divided into 6 groups with the random numbers table and the application will be made on different days and times. The application time is 10-15 minutes and the camera will be recorded during the interview. At the end of the application, standard patient feedback will be given for each student. At the end of the application, analysis sessions will be held with the students as a group and feedback will be given by peers and trainers about their own performances. Analysis sessions will take between 30-45 minutes.

Other: Standardized Simülation Patient

Control Group

NO INTERVENTION

No application will be made.

Interventions

Standardized Simülation Patient OTHER

There are preliminary information, information, application and analysis sessions in the research. A rehearsal will be made 10 days before the application and arrangements will be made if necessary. The students will be given the resources 1 week before the application and the scenario 5 minutes before the application and informed consent will be obtained. Just before the application, information about the simulation process and analysis will be given. Students will be divided into 6 groups with the random numbers table and the application will be made on different days and times. The application time is 10-15 minutes and the camera will be recorded during the interview. At the end of the application, standard patient feedback will be given for each student. At the end of the application, analysis sessions will be held with the students as a group and feedback will be given by peers and trainers about their own performances. Analysis sessions will take between 30-45 minutes.

Experimental Group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Having taken the course of Self-Knowledge and Communication Methods, Those who have not participated in a practical activity (course, simulation application, applied program, etc.) for communication skills No experience working in the intensive care unit 18 years and over, No written or verbal communication problems, Students who volunteer to participate in the research will be included in the research.

You may not qualify if:

• Having a psychiatric or neurological disease that will prevent the understanding and interpretation of the simulation application, Students who have problems in speaking/understanding Turkish will not be included in the study.

Sponsors & Collaborators

• Sinop University: lead

Study Sites (1)

Sinop University

Sinop, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Personal Satisfaction; Communication

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Ümran DEMİRCAN, Lecturer

CONTACT

05556395830; umrnaltinoz@gmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Lecturer

Model Details: randomized controlled experimental design

Study Record Dates

• First Submitted: March 21, 2023
• First Posted: April 7, 2023
• Study Start: April 20, 2023
• Primary Completion: April 25, 2023
• Study Completion: April 30, 2023
• Last Updated: April 7, 2023

Record last verified: 2023-04

Data Sharing

• IPD Sharing: Will share
• Shared Documents: ICF

Locations

TU (1)