Skin Cancer, Self Skin Examination and Sun Protection Behaviors Training (RCT)
Skin Cancer
About this trial
This is an interventional basic science trial for Skin Cancer focused on measuring Skin Cancer,, Nursing, skin self-examination, sun protection
Eligibility Criteria
Inclusion Criteria:
- To agree to participate in the research,
- Being a parent with a child between the ages of 10-14,
- Being open to communication and cooperation,
- Being able to read and write,
Exclusion Criteria:
- Having a situation that may prevent written and verbal communication,
- Not to have a child between the ages of 10-14,
- Not agreeing to participate in the research,
- Being illiterate,
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Education (Intervention) Group
Control Group
In the pretest phase of the research;Education group, those who signed the Informed Voluntary Consent Form and agreed to participate in the research will fill out the questionnaire.Data collection will take approximately 20-25 minutes.Afterwards,the researcher will give training to the training group about skin cancer,skin self-examination and sun protection behaviors.The tutorials are planned as a PowerPoint demonstration.The duration of the trainings is planned to take approximately 40minutes.The content of the training was prepared in line with the literature review.As a method;It will be in the form of narration,question and answer,brainstorming.Materials used in education;Colorfulbrochures on the subject will be given to reinforce the slide show and post-training information.A follow-up period of four months will be expected after the training given.At the end of the follow-up period,the training group will have to fill out the post-test questionnaires during the post-test phase.
Control Group: In the pre-test phase of the study; control group parents, those who signed the Informed Consent Form and agreed to participate in the study will fill out the questionnaire. Data collection will take approximately 20-25 minutes. During the follow-up period (120 days), no intervention will be made on the control group. At the end of the follow-up period (120 days), the control group will have to fill out the post-test questionnaires during the post-test phase. Participants will be reminded of the purpose of the research. Approval of the Informed Consent Form will be received. Completing the post-test questionnaires will take approximately 20-25 minutes. A brochure training material will be distributed to the parents of the control group, in line with the principle of equality, immediately after the completion of the post-tests.