Intestinal Cancer
Conditions
Keywords
Nursing, Navigation Program, Stoma, Compliance
Brief summary
This study was conducted as a randomized controlled intervention study with repetitive measurements in a pretest-posttest order to examine the effect of nurse navigation program on compliance, quality of life and prevention of complications in patients with intestinal stoma. The study was completed with 30 experimental and 28 control group patients with intestinal stoma in six hospitals, two of which are training and research hospitals, located in Gaziantep city center, between January 1 and December 31, 2021. While counseling, remote support, written and visual trainings, informative messages, phone calls, and appointment scheduling were applied to the patients in the experimental group within the scope of the nurse navigation program, the patients in the control group received standard care
Detailed description
This study was conducted as a randomized controlled intervention study with repetitive measurements in a pretest-posttest order to examine the effect of nurse navigation program on compliance, quality of life and prevention of complications in patients with intestinal stoma. The study was completed with 30 experimental and 28 control group patients with intestinal stoma in six hospitals, two of which are training and research hospitals, located in Gaziantep city center, between January 1 and December 31, 2021. While counseling, remote support, written and visual trainings, informative messages, phone calls, and appointment scheduling were applied to the patients in the experimental group within the scope of the nurse navigation program, the patients in the control group received standard care. The patients were evaluated using the Patient Information Form, Stoma Complications Evaluation Form, Stoma-Related Problems Experienced Form, Ostomy Compliance Scale, and Stoma Quality of Life Scale at the first interview, at the third and sixth months.
Interventions
BEHAVIORALimplementation of the nurse navigation program
Adult patients with intestinal stoma were contacted continuously for 6 months.
Sponsors
Kilis 7 Aralik University
Study design
Observational model
COHORT
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
with intestinal stoma * Having no mental handicap or perception problems and no communication difficulties * No psychiatric disease * 18 years old and over * literate * Capable of using a smartphone * No vision and hearing problems * Those who have the physical ability to change the stoma bag themselves. * Patients with intestinal stoma for a maximum of two months were included in the study.
Exclusion criteria
* After agreeing to participate in the research, wanting to leave, * Those who died during the research process, * The stoma was closed during the research process, * Patients whose communication could not be maintained during the research process
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| stoma compliance | 6 month | stoma compliance scale |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| life quality | 6 month | quality of life scale |
Countries
Turkey (Türkiye)
Outcome results
None listed