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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00569608
Other study ID # FIHLaFe
Secondary ID AP015/06
Status Completed
Phase N/A
First received December 6, 2007
Last updated December 6, 2007
Start date January 2005
Est. completion date October 2006

Study information

Verified date June 2005
Source Fundacion Para La Investigacion Hospital La Fe
Contact n/a
Is FDA regulated No
Health authority Spain: Comité Ético de Investigación Clínica
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 140
Est. completion date October 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 36 Weeks to 42 Weeks
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Other:
Early Discharge
Application of an early discharge protocol from the neonatal intensive care unit.

Locations

Country Name City State
Spain Hospital Universitario La Fe Valencia

Sponsors (1)

Lead Sponsor Collaborator
Fundacion Para La Investigacion Hospital La Fe

Country where clinical trial is conducted

Spain, 

References & Publications (3)

Psychological distress in parents of premature infants at discharge from the nicu. Saénz P1, Cerdá M1, Gorba M1, Díaz Cordobés JL2, Yi, P2, Barreto, P2 ;Vento M (Sponsored by Maximo V, Prof)1Servicio de Neonatología, Hospital Universitario Materno Infanti

Psychological follow up of parents of preterm infants enrolled in an early discharge program from the nicu. Saénz P1, Díaz Cordobés JL2, Cerdá M1, Boronat N1, Barreto P2, Yi P2; Vento M1. (Sponsored by Maximo Vento,)1Servicio de Neonatología, Hospital Uni

Vulnerability Of Parents Of Very Low Birth Weight Infants (Vlbw) During Nicu Hospitalization. Saénz P1, Díaz Cordobés JL2, Cerdá M1, Boronat N1, Yi P2, Barreto P2 ; Vento M1. (Sponsored by Maximo Vento, Prof)1 Servicio de Neonatología, Hospital Universita

Outcome

Type Measure Description Time frame Safety issue
Primary Reduction in the length of hospitalization. Days of hospitalization Yes
Secondary Parental stress up to 3 months post discharge No
Secondary Use of Health Resources of the Community up to 3 months post discharge No
Secondary Reduction in cost of hospitalization Reduction in euros/baby No
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