Ostomy care education to patients with intestinal ostomy

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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014113020162N1

Enrollment

Registered

2015-04-04

Start date

2015-04-05

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Ineffective training. other problems related to education and literacy

Interventions

Intervention 1: Intervention1: The demonstration- return demonstration ostomy care training is done in 4 sessions, in the first session teach about the types of ostomy, diet, bathing, authorized and u

Intervention1: The demonstration- return demonstration ostomy care training is done in 4 sessions, in the first session teach about the types of ostomy, diet, bathing, authorized and unauthorized acti

intervention2: The simulation ostomy care training is done in 4 sessions, in the first session teach about the types of ostomy, diet, bathing, authorized and unauthorized activities and warning signs,

Eligibility

Sex/Gender

All

Age

17 Years to 65 Years

Inclusion 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

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Self efficacy. Timepoint: Before the intervention, after the intervention, 1.5 month after intervention. Method of measurement: self efficacy questionnaire.	—

Secondary

Measure	Time frame
Adjustment. Timepoint: Before the intervention,After the intervention, 1.5 month after intervention. Method of measurement: Ostomy adjusment inventory 23 questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohre Pouresmail

Mashhad University of Medical Sience

pouresmailz921@mums.ac.ir+98 935 539 2288

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026