Viewing Study NCT06286176



Ignite Creation Date: 2024-05-06 @ 8:11 PM
Last Modification Date: 2024-10-26 @ 3:22 PM
Study NCT ID: NCT06286176
Status: COMPLETED
Last Update Posted: 2024-02-29
First Post: 2024-02-16

Brief Title: Breastfeeding Promotion in Lebanon Through a Salutogenic Intervention
Sponsor: Nabiha Ramadan
Organization: Lebanese International University

Study Overview

Official Title: Enhancing Breastfeeding Promotion in Lebanon Through a Salutogenic Intervention A Clinical Trial
Status: COMPLETED
Status Verified Date: 2024-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None