MedPath

Simulation-Based Learning Experience in Strengthening Stoma Care Education

Not Applicable
Not yet recruiting
Conditions
Stoma
Registration Number
NCT06749769
Lead Sponsor
Nuran Ayşen Pamir Aksoy
Brief Summary

The goal of this clinical trial is to investigate the effectiveness of simulation-based learning experience in enhancing stoma care education on patients with stoma.

The main hypothesis it aims to test are:

H1: Simulation-based learning experience is effective in reducing stoma patients' concerns about performing stoma care.

H2: Simulation-based learning experience is effective in increasing stoma patients' stoma care skills.

H3: Simulation-based learning experience is effective in increasing stoma patients' perceived self-efficacy regarding stoma care.

Researchers will compare the control and study group to see if the simulation-based learning enhances the patients learning experience.

Participants will be asked to;

* Answer the questions (demographic data form and anxiety scale)

* Receive education regarding stoma care (verbal and demonstration)

* Practice stoma care on their own

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
70
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Stoma Care Skills RubricPost-operative 3rd day

It consists of 23 items that include stoma care process steps. The learner's competence for each process step is scored between 0-2 (0- Insufficient 1- Partially sufficient 2- Sufficient). A minimum of 0 and a maximum of 46 points can be obtained. The total score shows the competence of stoma care skills.

Generalized Perceived Self-Efficacy Scaleat the time of enrollement, and Post-operative 3rd day

It consists of 10 items, and each item of the scale is scored between 1 and 4. These are listed as not true (1), somewhat true (2), more true (3), and completely true (4). Minimum of 10 and a maximum of 40 points can be obtained. The higher the score, the higher the individual's perceived self-efficacy.

Secondary Outcome Measures
NameTimeMethod
State Anxiety Levelat the time of enrollement, and post-operative 3rd day

In the study, the state anxiety scale will be used to determine the anxiety levels of the patients during the application. The State Anxiety Scale (SAS) provides information about what the individual feels at that moment. The State Anxiety Scale is a Likert-type scale consisting of 20 items, rated between 1 (not at all) and 4 (completely).

Trial Locations

Locations (2)

Acibadem Altunizade Hospital

🇹🇷

Istanbul, Other, Turkey

Acibadem Atakent Hospital

🇹🇷

Istanbul, Other, Turkey

© Copyright 2025. All Rights Reserved by MedPath