Preconceptional Period and Transtheoretically Based Education
NCT ID: NCT06765304
Last Updated: 2026-01-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
108 participants
INTERVENTIONAL
2025-11-17
2026-01-12
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect Web Based Pregnancy Preparation Education According to Health Promotion Model in Preconceptional Period on Women
NCT06044545
Web-based Preconceptional Care and Counseling, Risk Awareness, Healthy Lifestyle Behavior
NCT06002451
Women's Health Behaviors Stages of Change (Transtheoretical Model) in Preconception Period
NCT03893084
The The Effect of Planned Behavior Theory-Based Education on Physical Activity and Dysmenorrhea
NCT06210659
Health Promotion Model, Fertility Awareness, Preconception Knowledge and Attitude
NCT06690554
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Transtheoretically Based Education Model Intervention Group
Transtheoretical education intervention group
The training sessions will be held over four weeks in eight consecutive sessions (two sessions per week). Each session will last 60 minutes. The content of each training module will be designed under the following headings: Week 1 - Planning, Week 2 - Preparation, Week 3 - Action, Week 4 - Sustainability.
Preconceptional Period Healthy Life Behaviours Classical Education Intervention Group
Preconceptional Period Healthy Life Behaviours Classical Education Intervention Group
Participants will be provided with eight educational modules designed for the preconception period. Training sessions will be conducted twice weekly for 60 minutes over a four-week period.
Placebo Group
Placebo
No procedures will be performed on participants.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Transtheoretical education intervention group
The training sessions will be held over four weeks in eight consecutive sessions (two sessions per week). Each session will last 60 minutes. The content of each training module will be designed under the following headings: Week 1 - Planning, Week 2 - Preparation, Week 3 - Action, Week 4 - Sustainability.
Preconceptional Period Healthy Life Behaviours Classical Education Intervention Group
Participants will be provided with eight educational modules designed for the preconception period. Training sessions will be conducted twice weekly for 60 minutes over a four-week period.
Placebo
No procedures will be performed on participants.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being between the ages of 18-49 and not going through menopause
* Not having problems in speaking and understanding Turkish
* To be able to read and write
* Being sexually active
* Thinking about becoming pregnant in the next 2 years
* Having the risk score determined from the 'Preconceptional Risky Life Behaviours in Women Diagnostic Scale' to be developed by the researchers
Exclusion Criteria
* Having chronic diseases (diabetes, hypertension, hypothyroidism, etc.)
18 Years
49 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ankara Medipol University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Şerife İrem DÖNER
Research Assistant
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ankara Medipol University
Ankara, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
DönerKarahan24
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.