Clinical Trials Directory

Trials / Completed

CompletedNCT01859065

"Anticipatory Guidance in the Nursery and Its Impact on Non-urgent Emergency Department Visits"

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
323 (actual)
Sponsor
Bronx-Lebanon Hospital Center Health Care System · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

Kennedy et al, in a study of pediatric Emergency Department (ED) use by newborns less than 14 days of age, revealed that half of all visits in this population were non-acute problems. Other pediatric ED utilization studies have shown similar findings in that 32% to 72% of all visits were for non-urgent problems. Many studies have found that primiparity and young maternal age are associated with non-acute ED presentations. A recent factor that has been investigated is the effect of early neonatal discharge. Some other factors are nonwhite mothers and mothers on Medicaid. Zandieh et al, found additional predisposing determinants for non-urgent ED visits, such as single parenthood, Hispanic ethnicity, and having perceptions that their child's overall physical health was poor. Paradis et al found that parents receiving a video intervention rated higher confidence with specific infant care skills and reported feeling better prepared to care for their baby, compared to parents receiving only handouts. However, there isn't any reported study that evaluates the benefits of receiving both, a video intervention along with handouts. Aim: to demonstrate whether conducting anticipatory guidance related to non-urgent problems will reduce non-urgent ED visits, compared to care as usual (CAU) anticipatory guidance (Sudden Infant Death Syndrome and Shaken Baby Syndrome videos; and unstructured talk about jaundice, vaccinations, appointments, care of umbilical stump, normal urination and bowel movement, fever).

Detailed description

Inclusion Criteria: Mother of a newborn in the Well Baby Nursery (WBN) of Bronx-Lebanon Hospital Center during the 4-month recruitment period of the study. Exclusion Criteria: 1. Mothers selected for video-based anticipatory guidance that have a hearing/vision impairment. 2. Mothers selected for handout-based anticipatory guidance who speak a language other than Spanish or English. Primary outcome measure: reduction in non-urgent ED visits in mothers who received the intervention (video-based and handout-based anticipatory guidance regarding non-urgent problems), compared to the control group (received CAU anticipatory guidance) Secondary outcome measure: improvement in parental knowledge, attitude and behaviors related to non-urgent problems as a result of receiving anticipatory guidance (video and handouts) regarding non-urgent problems;

Conditions

Interventions

TypeNameDescription
BEHAVIORALIntensified anticipatory guidanceMothers receive video-based and handout-based anticipatory guidance regarding non-urgent problems in addition to the routine anticipatory guidance
BEHAVIORALRoutineRoutine anticipatory guidance (control)

Timeline

Start date
2011-12-01
Primary completion
2012-04-01
Completion
2012-04-01
First posted
2013-05-21
Last updated
2013-05-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01859065. Inclusion in this directory is not an endorsement.