Effectiveness of Chatbot-Supported Web Program in Postpartum Care
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Educational intervention.
- Who it may be relevant to
- Registry conditions: Postpartum Care, Web-based Training, Chatbot-Based Training. Basic parameters: 18 years — 35 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluation of the Effectiveness of a Chatbot-Supported Web-Based Postpartum Care Package Program for Postpartum Women
Overview
The purpose of this clinical study was to evaluate the effectiveness of a web-based "Postpartum Care Package" program developed for postpartum women and delivered via a chatbot, and to examine its effects on the postpartum health of mothers and newborns. 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?
Interventions
- Behavioral 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
Primary outcome measures
- Postpartum Physical Symptom Severity Scale [Time frame: Pre-test/24-48 hours postpartum Post-test/6 weeks and 3 months postpartum]
- Visual Analog Scale [Time frame: Pre-test/24-48 hours postpartum Post-test/6 weeks and 3 months postpartum]
- Edinburgh Postpartum Depression Scale [Time frame: Pre-test/24-48 hours postpartum Post-test/6 weeks and 3 months postpartum]
- Sexual Life Quality Scale [Time frame: Pre-test/24-48 hours postpartum Post-test/6 weeks and 3 months postpartum]
- Breastfeeding Self-Efficacy Scale [Time frame: Pre-test/24-48 hours postpartum Post-test/6 weeks and 3 months postpartum]
Secondary outcome measures (1)
- Postpartum care package program satisfaction [Time frame: 3rd month postpartum]
Eligibility criteria
Inclusion Criteria: Women who will be included in the study.
- Have given birth between the 37th and 41st weeks of pregnancy,
- 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 moved outside the province where the study was conducted during the implementation period,
- 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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07148778 · 17/04/2025-04/1228-AYBU-001