SuspendedNot Applicable

Simulation-Based Learning Experience in Strengthening Stoma Care Education

Stopped: Due to changes in the clinical research team. The surgeon responsible for performing the study-related procedures has left the study hospital. The research team is currently seeking an appropriately qualified investigator to resume the study.

Turkey (Türkiye)70 participantsStarted 2026-04

Plain-language 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

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

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

Exclusion criteria

. Patients who develop surgical complications in their stoma.
. Patients who are unable to perform stoma care due to any complication

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Stoma Care Skills Rubric

Timeframe: Post-operative 3rd day

Generalized Perceived Self-Efficacy Scale

Timeframe: at the time of enrollement, and Post-operative 3rd day

Trial details

NCT IDNCT06749769

SponsorNuran Ayşen Pamir Aksoy

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-12

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