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Early Hospital Discharge Program in Neonatology

Early Discharge Program From a Regional Reference Neonatal Intensive Care Unit

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00569608
Acronym
EDNEO
Enrollment
140
Registered
2007-12-07
Start date
2005-01-31
Completion date
2006-10-31
Last updated
2007-12-07

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

Conditions

Prematurity

Keywords

Parental stress, Early discharge, Anxiety, Depression, Neonatal Intensive Care Unit

Brief summary

Early discharge of premature infants from the Neonatal Intensive Care Unit will have substantial benefits: (i) diminish parental stress; (ii) increase parental - child bonding; (iii) diminish medical complications derived from prolonged hospitalization; (iv) reduce cost; (v) increase number of point of attendance disponible for future patients.

Detailed description

Extremely premature infants have to remain for very prolonged time in the hospital. As a consequence, difficulties for establishing an adequate parental-infant bonding arise causing a substantial parental stress manifested as anxiety and depression, and increasing the risk of short and longterm consequences (neglect, abuse, maltreatment, abandonment). In addition, prolonged hospital stay will increase the probability of having medical complications (infections, excessive blood tests or image studies) and the cost of staying. Once the baby has improved sufficiently early discharge may be given independently of the baby's weight. In order to be successful, caregivers, psychologist and parents have to put forward an established protocol to be able to face satisfactorily this situation. We hypothesize that, with an adequate Early Discharge Program, we could substantially reduce length of hospitalization, cost, and reduce parental stress.

Interventions

Application of an early discharge protocol from the neonatal intensive care unit.

Sponsors

Fundacion Para La Investigacion Hospital La Fe
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
36 Weeks to 42 Weeks
Healthy volunteers
No

Inclusion criteria

* Prematurity * No need for hospital support * Parents fulfill sociological score * Cooperation of primary care pediatrician

Exclusion criteria

* Active disease * Need for hospital intervention * Major congenital malformations * Chromosomopathies

Design outcomes

Primary

MeasureTime frame
Reduction in the length of hospitalization.Days of hospitalization

Secondary

MeasureTime frame
Parental stressup to 3 months post discharge
Use of Health Resources of the Communityup to 3 months post discharge
Reduction in cost of hospitalizationReduction in euros/baby

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026