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Trial Title:
The Effect of Cervical Cancer Awareness Education Based on Mobile Application
NCT ID:
NCT06252012
Condition:
Cervix Cancer
Cancer Awareness
Mobile Application
HPV
Nurse's Role
Conditions: Official terms:
Uterine Cervical Neoplasms
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Prevention
Masking:
Single (Participant)
Intervention:
Intervention type:
Behavioral
Intervention name:
Mobile application
Description:
The mobile application will be designed as a health assistant for women aged between
30-65 to encourage healthy choices and positively develop their behaviors regarding the
prevention of cancer. Within the scope of the mobile application, information modules on
cervical cancer screening tests, cervical cancer risk factors, ways to prevent cervical
cancer, types of HPV, and HPV vaccine will be provided. A parallel-group pretest-posttest
randomized controlled trial design will be used in the second stage of the study
Arm group label:
Mobile Application Group
Summary:
Cervical cancer is one of the most common cancer types affecting women in our country and
in the world and causing morbidity. However, the availability of a vaccine for cervical
cancer, preventable risk factors and early diagnosis tests offer a unique opportunity to
reduce the rate of cervical cancer. In this context, there are studies showing that the
practices developed by policies differ and that the classical health approach is
insufficient. The effectiveness of the trainings given may vary according to time, place,
trainer and personal characteristics of the individual. At the same time, in order to
improve the attitudes and behaviours of individuals in terms of prevention and early
diagnosis of cervical cancer, awareness of individuals about cervical cancer should be
increased. In this way, women will have a say about their own health and their conscious
participation in health care services will be realised. Therefore, the aim of this
project is to apply cervical cancer awareness training to women and to examine its effect
on women's cervical cancer prevention and early diagnosis behaviours. Original value; The
fact that there is no mobile application developed for cervical cancer in Turkey reveals
the national value of the research. In addition, the mobile application has international
unique value as it is the first mobile application structured to provide awareness on
cervical cancer prevention and early diagnosis behaviours. The project method was planned
for the development and implementation of the mobile application programme. The research
design will be a randomised controlled study. The 120 women who meet the inclusion
criteria and who apply to more than one family health centre will be randomly assigned to
the intervention and control groups. The effect of the mobile application programme on
women's attitudes and behaviours towards cervical cancer prevention and early diagnosis
will be evaluated at the 6th and 12th weeks. In the evaluation of the data, t-test for
independent groups, anova and chi-square tests will be used to measure the effect of the
intervention. Widespread effect; In this way, it is planned to reduce the time spent by
professionals for care-related activities, to strengthen time management, to provide
advantages and improvements in the performance of nurses in patient care management by
using technological resources in the health care provided.
Detailed description:
Cervical cancer is one of the most common cancer types affecting women in our country and
in the world and causing morbidity. However, the availability of a vaccine for cervical
cancer, preventable risk factors and early diagnosis tests offer a unique opportunity to
reduce the rate of cervical cancer. The World Health Organization launched the "global
strategy to accelerate the elimination of cervical cancer as a public health problem"
programme in 2020 to eliminate cervical cancer by 2030. In this context, there are
studies showing that the practices developed by policies differ and that the classical
health approach is insufficient. The effectiveness of the trainings given may vary
according to time, place, trainer and personal characteristics of the individual. At the
same time, in order to improve the attitudes and behaviours of individuals in terms of
prevention and early diagnosis of cervical cancer, awareness of individuals about
cervical cancer should be increased. In this way, women will have a say about their own
health and their conscious participation in health care services will be realised.
Therefore, the aim of this project is to apply cervical cancer awareness training to
women and to examine its effect on women's cervical cancer prevention and early diagnosis
behaviours. Original value; the fact that there is no mobile application developed for
cervical cancer in our country reveals the national value of the research. In addition,
the mobile application has an international unique value as it is the first mobile
application structured to provide awareness about cervical cancer prevention and early
diagnosis behaviours. It is thought that the mobile application programme to be developed
has a unique content that provides knowledge and skills to increase the health culture
and participation in health decisions thanks to its educational content such as cervical
cancer risk factors, prevention methods, diagnostic tests, test results, treatment
methods. In addition, it is the first mobile application developed in the
national/international field regarding cervical cancer prevention and early diagnosis
attitudes and behaviours in line with the deficiencies identified in the literature. The
project method was planned for the development and implementation of the mobile
application programme. The research design will be a randomised controlled study. A total
of 120 women who meet the inclusion criteria and apply to more than one family health
centre will be randomly assigned to the intervention (women who use the mobile
application programme) and control groups (women who receive the standard education
booklet). The mobile application programme includes a total of 12 interfaces for cervical
cancer prevention and early diagnosis of cervical cancer. The content of the interfaces
and the developed mobile application will be evaluated with the opinion of experts and
pre-application. The effect of the mobile application programme on women's attitudes and
behaviours towards cervical cancer prevention and early diagnosis will be evaluated in
the 6th and 12th weeks. In the evaluation of the data, t-test, anova and chi-square tests
for independent groups will be used to measure the effect of the intervention. Widespread
effect; In this way, it is planned to reduce the time spent by professionals for
care-related activities, to strengthen time management, to provide advantages and
improvements in the performance of nurses in patient care management by using
technological resources in the health care provided.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- She applied to Yıldırım Beyazıt Family Health Center and Zafertepe Family Health
Center in Kütahya.
- No pregnancy or malignancy,
- No hearing and vision problems,
- Between the ages of 30-65,
- Having a smart phone,
- sexually active
- Can read and write Turkish,
- Have not had a pap-smear test in the last 5 years,
Exclusion Criteria:
Pregnancy women Breastfeeding Have a history of cancer Have undergone hysterectomy
operation Those who have undergone an operation for cervical cancer (cryosurgery, etc.)
Gender:
Female
Gender based:
Yes
Gender description:
Since cervical cancer is seen in women, the study was based on gender.
Minimum age:
35 Years
Maximum age:
60 Years
Healthy volunteers:
Accepts Healthy Volunteers
Start date:
April 1, 2024
Completion date:
October 1, 2024
Lead sponsor:
Agency:
Kutahya Health Sciences University
Agency class:
Other
Collaborator:
Agency:
Akdeniz University
Agency class:
Other
Source:
Kutahya Health Sciences University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06252012