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Effectiveness of Chatbot-Supported Web Program in Postpartum Care

E

Emine Ilkin Aydin

Status

Not yet enrolling

Conditions

Web-based Training
Postpartum Care
Chatbot-Based Training

Treatments

Behavioral: Educational intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT07148778
17/04/2025-04/1228-AYBU-001

Details and patient eligibility

About

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?

Enrollment

102 estimated patients

Sex

Female

Ages

18 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

102 participants in 2 patient groups

Arm 1: Chatbot-Assisted Web-Based Postpartum Care Package Program
Experimental group
Treatment:
Behavioral: Educational intervention
Arm 2: Standard Postpartum Care
No Intervention group

Trial contacts and locations

0

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Central trial contact

Emine ILKIN AYDIN, Lecturer

Data sourced from clinicaltrials.gov

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