Clinical Trials Directory

Trials / Completed

CompletedNCT06690554

Health Promotion Model, Fertility Awareness, Preconception Knowledge and Attitude

The Effect of Education Given to Preconception Women in Line with the Health Promotion Model on Fertility Awareness, Preconception Knowledge and Attitude Levels

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
128 (actual)
Sponsor
Selcuk University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The effect of education given to preconceptional women in line with the health promotion model on fertility awareness, preconceptional knowledge and attitude levels

Detailed description

The research is a randomized controlled trial. The research will conducted with 128 women (intervention group n=64, control group n=64). It will consist of women between the ages of 18-35 who applied to the community health unit of Güneysınır District Health Directorate between December 2024-May 2025. Women who accept the research and are assigned to the intervention group will be given a five-day training to increase fertility awareness and preconceptional knowledge levels in line with the health promotion model. At the end of the fifth day, the Fertility Awareness Scale, Preconceptional Knowledge and Attitude Scale, and the Clinical Evaluation Form of the Health Promotion Plan for the Health Promotion Model will be applied to women who complete the training with a face-to-face interview technique. The women in the intervention group will be reached by phone at the end of the first and second months to remind them of their health promotion behaviors and to answer their questions and carry out follow-ups. At the end of the third month, women who have completed the training will be invited to the institution and the forms will be filled out again.

Conditions

Interventions

TypeNameDescription
OTHEREducation GroupWomen will be given a five-day training in line with the health promotion model. Information will be provided to women who apply to the hospital. Written consent documents will be obtained from women who agree to participate in the study. Women assigned to the intervention group will attend classes in groups of 8-10. Women will be given a 60-minute training once a day for five days. The total training duration is five hours. Scales will be applied to women who complete the training at the end of the fifth day. Women who have completed the training will be contacted by phone at the end of the first and second months, reminded of health promotion behaviors and their questions will be answered and follow-ups will be carried out. At the end of the third month, women who have received training will be invited to the institution and the Fertility Awareness, Preconceptional Knowledge and Attitude will be filled out face-to-face for the final test.

Timeline

Start date
2024-11-01
Primary completion
2025-03-01
Completion
2025-03-01
First posted
2024-11-15
Last updated
2025-03-20

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06690554. Inclusion in this directory is not an endorsement.