Effect of virtual breastfeeding counseling versus control group on self-efficacy and continuity of breastfeeding in nulligravida wome

Not Applicable

Recruiting

• Conditions: Breastfeeding difficulty.; Neonatal difficulty in feeding at breast; P92.5

• Registration Number: IRCT20120215009014N456
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 70

Inclusion Criteria

Age 18 to 40 years
Gestation age 36 to 48 weeks
First pregnancy
The possibility of using the Internet and WhatsApp
Being literate

Exclusion Criteria

High risk pregnancy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Breastfeeding self-efficacy. Timepoint: Before the intervention and 4 weeks after that. Method of measurement: Using Dennis questionnaire.;The type of infant feeding. Timepoint: before the intervention and 4 weeks after that. Method of measurement: Using a standardized questionnaire.