Motivational interviewing to improve postpartum contraception use
The Effect of Transtheoretical Model-Based Antenatal and Postnatal Motivational Interviewing on Contraceptive Self-Efficacy, Contraceptive Attitude and Contraceptive Use: A Randomized Controlled Trial
This study is testing if motivational counseling can help pregnant women use contraception more effectively after giving birth.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 72 (estimated) |
| Sex | Female |
| Sponsor | Gazi University Academic / other |
| Locations | 1 site (Ankara) |
| Trial ID | NCT06521138 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the impact of transtheoretical model-based motivational interviewing on postpartum contraception among women in their late pregnancy. A total of 72 women, between 28 to 32 weeks of gestation, will be randomly assigned to either an intervention group receiving motivational counseling sessions or a control group receiving routine care. The study aims to enhance contraceptive self-efficacy and attitudes, with outcomes assessed 12 weeks postpartum using various validated questionnaires. Data analysis will be conducted using SPSS by an independent statistical expert.
Who should consider this trial
Good fit: Ideal candidates are women who are 28 to 32 weeks pregnant, literate in Turkish, and willing to participate in follow-up.
Not a fit: Patients who do not have a sexual partner or who consent to female sterilization immediately after delivery may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve postpartum contraception use and help in planning healthier pregnancy intervals.
How similar studies have performed: Previous studies have shown that motivational interviewing can effectively enhance contraceptive use and self-efficacy, suggesting a promising approach in this context.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 28 to 32 weeks of gestation * At least literate in Turkish * Agree to participate in the study * Willing to participate in the postpartum follow-up * Having access to a smartphone Exclusion Criteria: * Women who do not have a sexual partner * Women who give consent for female sterilization immediately after delivery
Where this trial is running
Ankara
- Gazi University — Ankara, Turkey (Recruiting)
Study contacts
- Principal investigator: Aliye Dogan Gangal — Gazi University
- Study coordinator: Aliye Dogan Gangal, MSc
- Email: doganaliye05@gmail.com
- Phone: 905389662381
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.