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The Effect of WhatsApp-Based Education and Counseling on Breastfeeding Self-Efficacy, Body Satisfaction, Healthy Lifestyle Behaviors, and Weight Retention in Postpartum Women: A Randomized Controlled Trial

I

Inonu University

Status

Completed

Conditions

Breast Feeding
Weight Change
Body Image
Postpartum Period
Health Behavior
Post Partum

Treatments

Behavioral: education

Study type

Interventional

Funder types

Other

Identifiers

NCT07185906
IU-SBE-FB-01

Details and patient eligibility

About

Brief Summary:

This randomized controlled trial aimed to evaluate the effect of WhatsApp-based education and counseling on breastfeeding self-efficacy, body satisfaction, healthy lifestyle behaviors, and weight retention in postpartum women. The study was conducted between January and March 2025 at four Family Health Centers in Siirt, Turkey. A total of 120 postpartum women were randomly assigned to the intervention and control groups. The intervention group received an 11-week WhatsApp-based education program, including short videos and counseling sessions prepared under the guidance of the Health Promotion Model. Data were collected at baseline, 3 months, and 6 months using validated instruments: the Postnatal Breastfeeding Self-Efficacy Scale, the Body Satisfaction Scale, and the Health-Promoting Lifestyle Profile II. The primary outcomes were breastfeeding self-efficacy and body satisfaction, while secondary outcomes included healthy lifestyle behaviors and postpartum weight retention. The findings are expected to provide evidence for the effectiveness of mobile health interventions in improving maternal health outcomes during the postpartum period.

Enrollment

86 patients

Sex

Female

Ages

18 to 49 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Women in the postpartum period (within the first week after delivery)

    • Aged 18-49 years
    • Able to read and understand Turkish
    • Owning a smartphone with internet access and WhatsApp installed
    • Willing to participate in the study and provide informed consent

Exclusion criteria

  • Women with medical complications that prevent breastfeeding (e.g., serious maternal illness, contraindications to breastfeeding)

    • Infants with conditions that prevent breastfeeding (e.g., congenital anomalies affecting sucking or swallowing)
    • Women with severe psychiatric disorders or cognitive impairments that may interfere with participation
    • Women who do not agree to participate or withdraw consent during the study

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

86 participants in 2 patient groups

Experimental: WhatsApp-based Education and Counseling
Experimental group
Description:
Participants receive an 8-week WhatsApp-based education and counseling program in addition to routine postpartum care. The intervention includes short educational videos, weekly messages, and feedback provided through WhatsApp. Content covers breastfeeding techniques, recognition of infant hunger cues, milk expression and storage, management of common breastfeeding problems, healthy nutrition, body satisfaction, and postpartum weight management.
Treatment:
Behavioral: education
Control Group
No Intervention group
Description:
Participants receive routine postpartum care provided by Family Health Centers. They do not receive any structured WhatsApp-based education or counseling.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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