MedPath

Breastfeeding Promotion in Lebanon Through a Salutogenic Intervention

Not Applicable
Completed
Conditions
Breast Feeding
Salutogenesis
Exclusive Breastfeeding
Interventions
Behavioral: Whatsapp group
Behavioral: Videos with breastfeeding education material and encouraging messages
Registration Number
NCT06286176
Lead Sponsor
Nabiha Ramadan
Brief Summary

The study is a randomized control trial to assess the effect of a salutogenic intervention on breastfeeding initiation and duration of exclusive breastfeeding in Lebanon. In this Salutogenic intervention, infant feeding helpers will provide subjects of the intervention group breastfeeding related information , and will support these subjects by counseling and guiding them to find general resistance resources. This aims to increase sense of coherence and its parameters: comprehensibility, manageability and meaningfulness, which are the base of salutogenesis.

Detailed Description

Pregnant women were recruited in their 3rd trimester of pregnancy and were randomly assigned to either an intervention or control group.

Both groups received standard breastfeeding education at the maternity ward. Additionally, the intervention is based on informative and supportive videos and a whatsapp group for interpersonal support. Videos and whatsapp groups were created and moderated by Infant Feeding Helpers. These are women from the same socio-economical background as the subjects, and have previous history of breastfeeding a minimum of 6 months exclusive breastfeeding.

The aim of the intervention was to increase initiation and duration of breastfeeding by increasing comprehensibility, manageability and meaningfulness of the breastfeeding period and therefore by enhancing their sense of coherence.

Chi-squared tests were used for descriptive statistics, Wilcoxon test was used for pre- post results of SOC and (SE) within each group. The change in pre-post SOC, SOC parameters and SE scores between control and intervention groups was analyzed with Quade non parametric.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
101
Inclusion Criteria
  • Pregnant women
  • Singleton
  • Healthy
  • New born not admitted to Neonatal Intensive Care Unit
  • Residing in Lebanon
Exclusion Criteria
  • Pregnant with more than 1 fetus
  • Mothers with a health condition contraindicating breastfeeding
  • Newborn admitted to NICU

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Behavioral: Whatsapp groupWhatsapp group4 Whatsapp groups were created. Each Whatsapp group was moderated by 1 infant feeding helper. Each whatsapp group consisted of 10-15 subjects. Mothers asked breastfeeding related questions to infant feeding helpers and also exchange experience with the other mothers on the group. This is arm in applied in all subjects on the intervention group. Mothers of the intervention group joined their corresponding whatsapp group 10 days before expected delivery date and the duration of the intervention involving the whatsapp group was until 6 months postpartum.
Behavioral: videosVideos with breastfeeding education material and encouraging messages4 videos are created and distributed to subjects in the intervention group. Video 1: 10 days before delivery Video 2: the day of the delivery Video 3: 1 week postpartum Video 4: 1 month postpartum Videos content: encouraging message, information related to breastfeeding management This is arm in applied in all subjects on the intervention group
Primary Outcome Measures
NameTimeMethod
breastfeeding initiation1 hour after birth

Number of women who breastfed their infants within 1 hour after birth

Duration of Exclusive breastfeedingat 6 months postpartum

number of women who are exclusively breastfeeding at 6 months postpartum. Exclusive breastfeeding indicates feeding infants only breastmilk without any other complementary food nor beverage.

Secondary Outcome Measures
NameTimeMethod
Mean change in Self- esteem in participants from baseline to 6 months postpartumThe first measurement was taken 10 days before delivery and the second measurement was taken at 6 months postpartum

Measuring the scores of the Rosenberg Self Esteem Scale- 10 items. Scores are from 0 to 30. Higher scores indicate higher self esteem

The Change in Sense of Coherence (SOC) scores from baseline to 6 months postpartum1st measurement: 10 days before delivery. 2nd measurement: 6 months postpartum. Score measurements were taken twice per subject for comparison at the end of the intervention.

The score of the "Sense of Coherence- 13 items" questionnaire. The minimum score is 13, and the maximum score is 91. Higher score indicates higher sense of coherence

Trial Locations

Locations (1)

Lebanese International University

🇱🇧

Beirut, Lebanon

© Copyright 2025. All Rights Reserved by MedPath