Clinical Trial: Development and Evaluation of an Interconception Care Educational Program on Hypertensive Disorders of Pregnancy for Postpartum Women: A Feasibility Study (Japan)

Tokyo, May 26 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061649) titled 'Development and Evaluation of an Interconception Care Educational Program on Hypertensive Disorders of Pregnancy for Postpartum Women' on May 25.

Study Type: Interventional

Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled

Primary Sponsor: Institute - St.Luke's international university

Condition: Condition - Hypertensive Disorders of Pregnancy Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - Develop an educational program on interconception care aimed at improving knowledge and preventing hypertensive disorders of pregnancy among women with prior childbirth experience, and evaluate its acceptability and feasibility from the perspectives of both postpartum women and midwives, while also exploratorily examining its limited effectiveness. Basic objectives2 - Safety,Efficacy

Intervention: Interventions/Control_1 - Participation in an educational program (the "HDP Future Project") consisting of the provision of a pamphlet and video materials on hypertensive disorders of pregnancy, followed by a midwife-led discussion session after completion of the learning materials.

Eligibility: Age-lower limit - Not applicable Age-upper limit - Not applicable Gender - Female Key inclusion criteria - 1. Women with prior childbirth experience Inclusion criteria Women who have had a childbirth experience within the past 3 years Women who have provided informed consent to participate in this study Women who are able to understand and respond to questionnaires written in Japanese Women who are able to use the internet

2. Midwives Midwives who cooperated in this program as research assistants and have at least 3 years of clinical experience Key exclusion criteria - No exclusion criteria were applied in this study. Target Size - 77

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2026 Year 04 Month 14 Day Anticipated trial start date - 2026 Year 06 Month 30 Day Last follow-up date - 2026 Year 10 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070119

Disclaimer: Curated by HT Syndication.