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Breastfeeding Promotion in Lebanon Through a Salutogenic Intervention

Enhancing Breastfeeding Promotion in Lebanon Through a Salutogenic Intervention: A Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06286176
Enrollment
101
Registered
2024-02-29
Start date
2022-11-17
Completion date
2023-06-30
Last updated
2024-02-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Feeding, Exclusive Breastfeeding, Salutogenesis

Keywords

Breastfeeding, Salutogenesis, Sense of coherence

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.

Interventions

BEHAVIORALVideos with breastfeeding education material and encouraging messages

Distributed videos aim to increase breastfeeding related knowledge and to receive support

BEHAVIORALWhatsapp group

The Whatsapp group is used in the intervention as a platform for interpersonal exchange of information and experience, in addition to peer support.

Sponsors

Universitat de Girona
CollaboratorOTHER
Nabiha Ramadan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
breastfeeding initiation1 hour after birthNumber of women who breastfed their infants within 1 hour after birth
Duration of Exclusive breastfeedingat 6 months postpartumnumber 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

MeasureTime frameDescription
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 postpartumMeasuring 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

Countries

Lebanon

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026