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Simulation-Based Learning Experience in Strengthening Stoma Care Education

Investigation of the Effectiveness of Simulation-Based Learning Experience in Strengthening Stoma Care Education on Patients With Stoma

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06749769
Acronym
SIMESEP
Enrollment
70
Registered
2024-12-27
Start date
2026-04-30
Completion date
2026-12-31
Last updated
2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stoma

Keywords

stoma care, patient education, simulation, patient's learning experience, Strengthening patients

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

Interventions

Patients will learn how to care for their stomata on a stoma simulator

Sponsors

Nuran Ayşen Pamir Aksoy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age 18 and above 2. First time having a stoma and having an intestinal stoma, 3. Communicable, open to cooperation, 4. Able to speak and understand Turkish, 5. Individuals who are willing to participate in the research and willing to be interviewed will be included in the research.

Exclusion criteria

1. Patients who develop surgical complications in their stoma. 2. Patients who are unable to perform stoma care due to any complication 3. Having previously received stoma care training or participated in its implementation for any reason

Design outcomes

Primary

MeasureTime frameDescription
Stoma Care Skills RubricPost-operative 3rd dayIt 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 dayIt 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

MeasureTime frameDescription
State Anxiety Levelat the time of enrollement, and post-operative 3rd dayIn 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).

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026