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Clinical Trial Summary

The primary aim of this study is to evaluate whether remote education is as effective as in-person education in improving self-care behaviors of ostomy patients.


Clinical Trial Description

After signing the informed consent form, patients with ostomy will be assigned to the intervention or active control group (1:1). The intervention group will receive a total of four remote educational sessions over 2 months. The control group will receive the standard care, consisting of in-person standard education. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05796544
Study type Interventional
Source University of Rome Tor Vergata
Contact Ercole Vellone, Professor
Phone +390672596871
Email ercole.vellone@uniroma2.it
Status Recruiting
Phase N/A
Start date June 14, 2023
Completion date April 1, 2025

See also
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