Tokyo, Oct. 17 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059364) titled 'Effectiveness of Providing Information on Preparing for Pregnancy and Having Children for Individuals with Spina Bifida' on Oct. 17.
Study Type:
Interventional
Study Design:
Basic Design - Single arm
Randomization - Non-randomized
Blinding - Open -no one is blinded
Control - Self control
Primary Sponsor:
Institute - Ibaraki Prefectural University of Health Sciences
Condition:
Condition - Spina bifida
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To evaluate the effectiveness of on-demand education for individuals with spina bifida regarding preparation for pregnancy and parenthood, and to gain insights into effective methods for providing information.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Participants will have the opportunity to view informational materials, including pamphlets or videos, that focus on preparing for pregnancy and having children. These materials will be available for a period of three months. Following a three-month hiatus, they will resume viewing or watching the other type of media they had not viewed or watched for the previous three months.
Eligibility:
Age-lower limit - 18
years-old
=
Gender - Male and Female
Key inclusion criteria - Individuals with spina bifida
Key exclusion criteria - Women who have experienced pregnancy, childbirth, infertility counseling, or infertility treatment, and men who currently have children and have experienced infertility counseling or infertility treatment
Target Size - 40
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 10 Month 10 Day
Anticipated trial start date - 2025 Year 12 Month 01 Day
Last follow-up date - 2027 Year 01 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067896
Disclaimer: Curated by HT Syndication.
