
Nursing open (PubMed)··Research ArticlePractice applicable
Wound and ostomy nurses help patients build confidence with equipment before they must manage a new stoma at home. The trial supports hands-on rehearsal as an addition to the established teaching pathway while keeping the evidence focused on early skills, adjustment, anxiety, and satisfaction.
Med-SurgPatients at two university hospitals were randomized to standard care alone or standard care plus preoperative belt-based practice. The intervention group had higher stoma-care skill and adjustment scores at every postoperative assessment, lower anxiety from discharge through day 30, and higher satisfaction at the preoperative and discharge assessments. The study evaluated short-term patient-reported and skill outcomes rather than complications or readmissions.
Key takeaways
- The trial randomized 170 patients preparing for intestinal stoma surgery at two university hospitals.
- The training belt allowed preoperative practice without applying an adhesive system directly to the abdomen.
- Skill and adjustment scores favored belt-based practice at discharge and through 30 days after discharge.
- The abstract does not establish effects on stoma complications, healthcare use, or outcomes beyond the first postoperative month.
Why this matters on shift
Wound and ostomy nurses help patients build confidence with equipment before they must manage a new stoma at home. The trial supports hands-on rehearsal as an addition to the established teaching pathway while keeping the evidence focused on early skills, adjustment, anxiety, and satisfaction.
Bedside takeaway
Hands-on preoperative stoma practice improved early skills and adjustment, but clinical and longer-term outcomes were not measured.
Nursing implications
- When an approved simulation device is available, integrate supervised practice into the existing preoperative stoma-education plan. Observe the patient's technique, revisit difficult steps before discharge, and arrange follow-up for ongoing skill or adjustment concerns.
Limitations & cautions
- The trial was conducted in general-surgery departments at two university hospitals and followed patients for 30 days after discharge. The abstract does not report blinding, clinical complications, readmissions, long-term self-management, or whether the findings generalize to other devices, stoma types, or care settings.
- AI-summarized from the linked source. Review the original article before applying to practice.
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AI-summarized from the linked source. Review the original article before applying to practice.













































