Colostomy
Conditions
Interventions
Intervention 1: Intervention group: (Pre-surgery training In addition to usual training) The patients who are allocated in the intervention group will be invited to participate in an ostomy care train
The membership link will only be available to patients of the intervention group or one of their family members (if the patient wishes). The time of use of educational materials will be at the disposa
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age 18 to 65 years Lack of cognitive or mental impairment Ability to verbal communicate
Exclusion criteria
Exclusion criteria: Performing emergency surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The ostomy self-efficacy: The Ostomy self-efficacy is equal to the score obtained by the patient in the ostomy self-efficacy questionnaire. The questionnaire has 22 items in a 5-item Likert scale. The questionnaire is in two dimensions includes ostomy care self-efficacy (13 items) and social self-efficacy (9 items). A higher score indicates higher self-efficacy. The lowest score that can be obtained in this tool is 22 and the highest score is 110. Timepoint: The stoma self-efficacy questionnaire will complete by patients before surgery and one month after surgery. Method of measurement: The stoma self-efficacy scale was designed and psychometrically evaluated by Beckers et al. (1996). The questionnaire has 22 items in two dimensions, including ostomy care self-efficacy (first 13 items) and social self-efficacy (next 9 items). Using a Likert scale, the answers are defined from not sure at all (score 1) to completely sure (score 5). A higher score indicates greater ostomy self-efficacy. The lowest score that can be obtained in this tool is 22 and the highest score is 110. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hospitalization time. Timepoint: One month after surgery. Method of measurement: Clinical records and patient interview.;The number of readmissions. Timepoint: One month after surgery. Method of measurement: Clinical records and patient interview.;The number of emergency visits. Timepoint: One month after surgery. Method of measurement: Clinical records and patient interview.;Peristomal skin condition. Timepoint: One month after surgery. Method of measurement: DET ostomy skin tool. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahnaz Ilkhani
Shahid Beheshti University of Medical Sciences
Outcome results
None listed