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Women on Breast Cancer Health Belıefs and Screenıng Behavıors

A

Ataturk University

Status

Completed

Conditions

Breast Cancer Female

Treatments

Other: Education

Study type

Interventional

Funder types

Other

Identifiers

NCT05677737
nihan25

Details and patient eligibility

About

Method: It was conducted in a randomized controlled experimental type. The population of the study consisted of 2426 women over the age of 20 living in a family health center in Erzurum between October 2021 and September 2022. The sample of the study consisted of 252 women with 0.05 margin of error and 95% confidence level, according to the sample size calculation formula used in cases where the universe is known. Within the framework of the exclusion criteria of the study, 52 women were excluded from the study and 200 women were included in the randomization.

Full description

Persons in the experimental group will be trained 6 times with an interval of 2 weeks via an online platform (zoom, etc.). No training will be given to the control group, and the post-test data will be collected by re-administering the two groups with the mid-test created via Google forms and containing the scales immediately after the training, and the "Health Belief Model Scale in Breast Cancer Screening" and "Breast Cancer Screening Beliefs Scale" two months later.

Enrollment

165 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

-Being over 18 years old

  • Being literate,
  • Computer can be used,
  • Internet is accessible,
  • Not getting breast cancer before,

Exclusion criteria

  • Having received training on breast cancer before

    • Having a history of breast cancer in first degree relatives
    • Those who did not attend all of the online trainings in the experimental group

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

165 participants in 2 patient groups

Experimental
Experimental group
Description:
In the study, the women in the experimental group will be trained every two weeks for 6 weeks.
Treatment:
Other: Education
Control
No Intervention group
Description:
No intervention will be applied to the control group.

Trial contacts and locations

1

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Central trial contact

Nihan Türkoğlu

Data sourced from clinicaltrials.gov

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