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.