Breastfeeding Education in the Time of COVID-19

NCT ID: NCT04519216

Last Updated: 2025-04-23

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

46 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-07-31

Study Completion Date

2021-12-10

Brief Summary

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This project will establish that pediatric and family medicine residents who complete a hybrid breastfeeding medicine curriculum that includes an asynchronous unfolding case scenario along with telesimulation with a standardized patient (SP) will provide timely, skilled lactation support more frequently than residents randomized to an asynchronous unfolding case scenario followed by videoconference group discussion regarding care for the breastfeeding dyad.

Detailed Description

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1. Establish that pediatric and family medicine residents who complete a novel breastfeeding medicine curriculum that includes an online unfolding case scenario along with telemedicine simulation with a standardized patient (SP) will provide timely, skilled lactation support more frequently than residents randomized to an online unfolding case scenario followed by traditional didactic breastfeeding case-presentation via videoconference.
2. Establish that online learning via unfolding case scenario and telemedicine simulation with a SP will be feasible for family medicine and pediatric residents to complete during their newborn nursery rotation.

Intern and third year residents completing their newborn nursery rotation at UC Davis Medical Center will be cluster-randomized by rotation month to receipt of breastfeeding education via telesimulation with standardized patient or traditional case-based learning via videoconferencing with pediatric faculty. The primary outcome of this study will be the translation of clinical lactation skills to the care of breastfeeding mothers and newborns. I hypothesize that pediatric and family medicine residents randomized to complete the telesimulation with SP will translate their acquired clinical lactation skills to the care of breastfeeding mothers and newborns at a greater rate than residents who complete a videoconference case-based traditional curriculum discussion with a newborn nursery pediatrician.

Conditions

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Breastfeeding Breastfeeding, Exclusive Breastfeeding Jaundice Educational Problems

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This is a prospective cluster randomized controlled trial of a novel educational intervention in pediatric and family medicine residents during the nursery rotation. In this study, we will enroll 1st year pediatric and family medicine residents and 3rd year supervising pediatric residents on their newborn nursery 4-week rotation and randomization will occur clustered by rotation month. The educational intervention will be conducted during the first week of the rotation. Both groups will complete pre-intervention survey that collects demographic information, personal infant feeding experiences, and any breastfeeding medicine experience. All participants will be invited to complete a free online course (Lactation Support in a Telehealth Setting Course) prior to the telemedicine intervention or control group discussion with the clinical pediatrician.
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors
Outcomes are blinded to the assessor when completing the trial data analysis.

Study Groups

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Traditional education

Participants in the control group will complete an online unfolding case scenario. Then these same participants will participate in a videoconferencing case based lecture with the academic pediatric fellow

Group Type ACTIVE_COMPARATOR

Telesimulation

Intervention Type BEHAVIORAL

Telesimulation educational intervention

Telesimulation

Participants in the intervention group will complete an online unfolding case scenario. Then these participants will complete a telesimulation case with a standardized patient via video conferencing.

Group Type EXPERIMENTAL

Telesimulation

Intervention Type BEHAVIORAL

Telesimulation educational intervention

Interventions

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Telesimulation

Telesimulation educational intervention

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Inclusion Criteria: Pediatric and Family Medicine resident physicians at UC Davis Medical Center 2.

Exclusion Criteria

Exclusion criteria: Individuals who are unable to communicate in English, Individuals who do not have access to videoconferencing via computer or phone.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of California, Davis

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Adrienne Hoyt-Austin, DO

Role: PRINCIPAL_INVESTIGATOR

University of California, Davis

Locations

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University of California - Davis

Sacramento, California, United States

Site Status

Countries

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United States

Other Identifiers

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1613611

Identifier Type: -

Identifier Source: org_study_id

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