Web-based Breastfeeding Education for Adolescent Mothers

NCT ID: NCT06748300

Last Updated: 2024-12-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

128 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-05

Study Completion Date

2024-11-25

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The present study was conducted as a randomized controlled trial to evaluate the effectiveness of web-based and face-to-face breastfeeding education given to primipara adolescent pregnant women. The study was conducted between March 2023 and December 2023 at the University of Health Sciences Van Training and Research Hospital Obstetrics and Gynecology Polyclinics. A total of 135 primipara adolescent pregnant women who met the inclusion criteria were included in the study, including 45 in the Booklet Supported Face-to-Face Breastfeeding Education Program (KİDYEP), 45 in the Web-Based Video Supported Breastfeeding Education Program (WEBVİDEP) and 45 in the control group. Pre-test data were collected in the third trimester by applying socio-demographic data form, breast milk and breastfeeding information form, and breastfeeding self-efficacy short form scale (antenatal form) to the groups. After the pre-test data were collected, a face-to-face breastfeeding education program with a breastfeeding education booklet was administered to the KİDYEP group, and a web-based video-assisted breastfeeding education program was administered to the WEBVİDEP group. Data were collected by applying breast milk and breastfeeding information form, LATCH breastfeeding identification and evaluation scale and breastfeeding self-efficacy short form scale (postnatal version) to the groups at the first (midtest) and sixth (posttest) weeks after delivery. As a result of the present study, the rate of exclusive breastfeeding, the total duration of considering breastfeeding, breast milk and breastfeeding knowledge levels, breastfeeding self-efficacy levels and breastfeeding success of the mothers in the KİDYEP and WEBVİDEP groups were found to be higher than the control group, and both the booklet-supported face-to-face breastfeeding education program and the web-based video-supported breastfeeding education program were found to be similarly effective.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Breastfeeding

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Web taban

Group Type EXPERIMENTAL

web- based education

Intervention Type BEHAVIORAL

breastfeeding education

face to face

Group Type EXPERIMENTAL

web- based education

Intervention Type BEHAVIORAL

breastfeeding education

control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

web- based education

breastfeeding education

Intervention Type BEHAVIORAL

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

face to face education

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Aged between 15 and 19 years
* Being 19 years old and above
* Being literate
* Being primigravida
* Having a single baby (not twins or more)
* Being a volunteer to participate in the study
* Having no health problems for the mother and the baby
* Having a computer, tablet or smart phone and the ability to use it
* Having regular internet access

Exclusion Criteria

* The mother being 18 years of age or younger
* Being multigravida and/or multiparous
* Having a health problem related to the mother or the baby
* Not having a smart phone or wireless internet during the study period
* Not filling out the survey forms incompletely and not watching videos about hygienic care of the newborn
Minimum Eligible Age

15 Years

Maximum Eligible Age

19 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Yuzuncu Yıl University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Emine Kurtcan

Asst. Prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Emine KURTCAN

Van, Lütfen Seçiniz., Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Web-Taban

Identifier Type: -

Identifier Source: org_study_id