The Effect of an Educational Video on Long-Acting Reversible Contraception (LARC) Utilization at 6-8 Weeks Postpartum Period: A Randomized Controlled Trial

Not Applicable

Completed

• Conditions: ARC utilization, reason for not using LARC; LARC utilization&#44

• Registration Number: TCTR20171225001
• Lead Sponsor: Faculty of Medicine Ramathibodi Hospital, Mahidol University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2016-03-01
• Study Start: 2017-12-25
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 270

Inclusion Criteria

Delivery of a live infant ≥ 24 weeks gestational age
Age ≥ 20 years old
Ability to communicate in Thai fluently
Willing to be contacted by phone until at least 8 weeks after delivery

Exclusion Criteria

History of female or male sterilization
Having contraindications for LARC

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
the percentage of participants who actually used LARC at 6-8 postpartum period ุ6-8 weeks postpartum periods Questionnaire

Secondary Outcome Measures

Name	Time	Method
reasons for not using LARC ุ6-8 weeks postpartum periods percentage of reason for not using LARC