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

Effect of virtual breastfeeding counseling versus control group on self-efficacy and continuity of breastfeeding in nulligravida women: a randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120215009014N456

Enrollment

Registered

2023-01-09

Start date

2023-01-21

Completion date

Unknown

Last updated

2023-02-07

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

Conditions

Breastfeeding difficulty. Neonatal difficulty in feeding at breast

Interventions

Intervention 1: Intervention group: Routine care during breastfeeding in addition to intervention in the form of a face-to-face breastfeeding counseling session for 45 to 60 minutes once a week in the

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

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

Exclusion criteria: High risk pregnancy

Design outcomes

Primary

Measure	Time frame
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.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehnoosh Jalili Khoei

Hamedan University of Medical Sciences

behnoosh.jalili@yahoo.com+98 81 3838 0572

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026