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Implementation of the Nurse Navigation Program

NCT05809661 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 58

Last updated 2023-04-12

No results posted yet for this study

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

Conditions

  • Intestinal Cancer

Interventions

BEHAVIORAL

implementation of the nurse navigation program

Adult patients with intestinal stoma were contacted continuously for 6 months.

Sponsors & Collaborators

  • Kilis 7 Aralik University

    lead OTHER

Principal Investigators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-01-01
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05809661 on ClinicalTrials.gov