Tokyo, March 24 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061026) titled 'Development of Educational Materials for Training Healthcare Professionals in Birth Review Practice During the Perinatal Period' on March 23.

Study Type: Interventional

Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Open -no one is blinded Control - No treatment

Primary Sponsor: Institute - St. Luke's Internatilnal University

Condition: Condition - Not applicable Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The aim of this study is to develop an educational program for midwives and midwifery students to support the appropriate implementation of birth review and to evaluate its effectiveness and feasibility in clinical practice. Basic objectives2 - Others

Intervention: Interventions/Control_1 - Participants in the intervention group will receive a video-based educational program developed to support the appropriate implementation of birth review. After allocation, participants will be instructed to view the assigned video within 1 week. The program is intended to be viewed once; however, repeated viewing within the intervention period will be allowed to facilitate understanding. Interventions/Control_2 - Participants in the control group will be assigned to a waiting-list condition. During the 1-week intervention period after allocation, no educational video will be provided, and participants will complete assessments at corresponding time points. After completion of the 1-month follow-up assessment, they will be offered the same video-based educational program as the intervention group.

Eligibility: Age-lower limit - 20 years-old = Gender - Female Key inclusion criteria - Participants who meet all of the following criteria will be included:

1.Midwives involved in perinatal care or students enrolled in a midwifery training program 2.Able to view the educational video on birth review 3.Aged 20 years or older at the time of consent 4.Provided informed consent electronically (Employment setting or workplace will not be restricted) Key exclusion criteria - Participants meeting any of the following criteria will be excluded:

1.Self-reported difficulty in viewing the educational material or completing the online questionnaire 2.Difficulty understanding Japanese or responding to the questionnaire 3.Self-reported high risk of psychological burden associated with participation 4.Considered inappropriate for participation by the principal investigator Target Size - 130

Recruitment Status: Recruitment status - Open public recruiting Date of protocol fixation - 2026 Year 03 Month 09 Day Date of IRB - 2026 Year 03 Month 09 Day Anticipated trial start date - 2026 Year 03 Month 23 Day Last follow-up date - 2026 Year 05 Month 10 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000069026

Disclaimer: Curated by HT Syndication.