Effectiveness of Chatbot-Supported Web Program in Postpartum Care
NCT ID: NCT07148778
Last Updated: 2025-08-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
102 participants
INTERVENTIONAL
2025-10-01
2026-12-01
Brief Summary
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The key questions it aims to answer are:
* What is the impact of the chatbot-supported web-based "Postpartum Care Package" program on the postpartum health of mothers and newborns?
* Does the chatbot-supported web-based "Postpartum Care Package" program increase women's accessibility and availability of postpartum care resources?
Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Arm 1: Chatbot-Assisted Web-Based Postpartum Care Package Program
Educational intervention
In this study, a web-based postpartum care package program supported by a chatbot will be administered to the intervention group.
A pre-test will be administered to participants in the intervention group within 24-48 hours after birth.
Participants in this group will be informed that they must watch the videos in the educational modules until the sixth week postpartum. Reminder messages will also be sent to participants via the website, email, and phone calls (between days 7 and 14 postpartum and week 3 postpartum). Participants who have completed the module training will be eligible for post-tests at 6 weeks postpartum and 3 months postpartum.
Arm 2: Standard Postpartum Care
No interventions assigned to this group
Interventions
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Educational intervention
In this study, a web-based postpartum care package program supported by a chatbot will be administered to the intervention group.
A pre-test will be administered to participants in the intervention group within 24-48 hours after birth.
Participants in this group will be informed that they must watch the videos in the educational modules until the sixth week postpartum. Reminder messages will also be sent to participants via the website, email, and phone calls (between days 7 and 14 postpartum and week 3 postpartum). Participants who have completed the module training will be eligible for post-tests at 6 weeks postpartum and 3 months postpartum.
Eligibility Criteria
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Inclusion Criteria
* Be primigravida,
* Have not been diagnosed with a high-risk pregnancy,
* Have an educational level of primary school or above,
* Have no communication difficulties or mental disabilities,
* Have access to equipment (mobile phone, computer, tablet, internet) for web-based education,
* Have experienced no complications in the mother or baby during pregnancy, childbirth, or the postpartum period,
* Voluntarily agree to participate in the study,
Exclusion Criteria
* Women who voluntarily withdrew from the study,
* Women who did not participate in any phase of the study will not be included in the study.
18 Years
35 Years
FEMALE
No
Sponsors
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Emine Ilkin Aydin
OTHER
Responsible Party
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Emine Ilkin Aydin
Lecturer
Principal Investigators
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Emine ILKIN AYDIN, Lecturer
Role: PRINCIPAL_INVESTIGATOR
Yozgat Bozok University
Central Contacts
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Other Identifiers
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17/04/2025-04/1228-AYBU-001
Identifier Type: -
Identifier Source: org_study_id