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Clinical Trials/IRCT2014113020162N1
IRCT2014113020162N1
Completed
未知

Comparitive study on the effects of simulation and demonstration-return demonstration methods in ostomy care training on self-efficacy and adjustment in patients with an intestinal stoma

Mashhad University of Medical Sciences0 sites46 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Ineffective training.
Sponsor
Mashhad University of Medical Sciences
Enrollment
46
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria for patients recently have ostomy surgery: Between 18 and 65 years old; Patient that Singed Consent Knowingly; Having healthy vision and hearing and having no disability; Have no psychological disease, movement disability and balance disorders; Have no experience of having intestinal ostomy in family members; Do not receive any regular and documented ostomy training.
  • Inclusion criteria for patients who already have ostomy surgery: Between 18 and 65 years old; Patient that Singed Consent Knowingly. Exclusion criteria: Willingness to continue participation in the study; Complications that commonly affect the Regular care and need to hospitalization; Patient death

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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