The Effect of Mobile-Based Education Given to Patients Undergoing Gynecological Oncology Surgery on Quality of Life

Sponsor
Istanbul University - Cerrahpasa
Study ID
NCT05694208
Status
Recruiting
Apply to this trial

Conditions

  • Gynecologic Cancer

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Education Group — BEHAVIORAL
    In the first pre-operative interview at the gynecological oncology outpatient clinic of the relevant hospital, the purpose of the research will be explained to the patients and an informed consent form will be filled. The patients in the experimental group will use the mobile-based care support application developed within the scope of the research.

Study Details

This study was planned in a randomized controlled prospective experimental design in order to determine the effect of mobile-based education given to patients undergoing gynecological oncology surgery on quality of life. Research Hypotheses: H1. Education given with mobile application in gynecological oncology patients positively affects symptom control of patients. H2. The education given with the mobile application in gynecological oncology patients positively affects the quality of life of the patients.

Key Dates

First listed
Jan 23, 2023
Start date
Feb 1, 2023
Status verified
Nov 2024
Primary completion
Dec 30, 2024
Completion
Jan 1, 2025

Study Design

Enrollment
84 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Experimental group
    The patients in the experimental group will use the mobile-based care support application developed within the scope of the research.
  • No Intervention: Control Group
    It is the group in which no intervention will be made other than data collection.

Primary Outcome Measure

The education given with the mobile application in gynecological oncology patients positively affects the quality of life of the patients. [ Time Frame: Women will be evaluated two weeks after surgery. ]

Central Contacts

Related Studies