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NCT00320840 Clinical Trial

Internal and Familial Resources and Motherhood. Follow Up of Mothers With Twins and Preterm Infants Versus Mothers With Single Full Term Infants

Preterm Infants Clinical Trial

Official title:
The Contribution of Internal and Familial Resources to the Development of Motherhood. Long Term Follow Up of Mothers With Twins and Preterm Infants Versus Mothers With Single Full Term Infants

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT00320840
Other study ID # SHEBA-06-4131-JK-CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received April 30, 2006
Last updated April 30, 2006
Start date May 2006
Est. completion date May 2012

Study information
Verified date April 2006
Source Sheba Medical Center
Contact Jacob kuint, MD
Phone 972-3-5303030
Email kuint-j@sheba.health.gov.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

To evaluate the contribution of internal and familial resources on the development of motherhood in a population of mothers having preterm twin infants and comparing this population to a population of mothers giving birth to single (or twins) full term infants.

Description:

150 mothers will participate in this study. The study is using 4 questionnaires at infants ages of 1 month, 1 year, 2 years and 4 years. The questionnaires are involving communication skills,grandparents support, stress feelings, psychological parameters, parity functioning, infant temperament, self assessment, maternal and infant medical background and twins and brotherhood evaluation.

a comparison will be done between mothers to preterm twins and mothers to single full term infants.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 150
Est. completion date May 2012
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A to 3 Months
Eligibility Inclusion Criteria:

- preterm infants

- twins

Exclusion Criteria:

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Sheba medical center - Neonatal Department Ramat -Gan

Sponsors (1)
Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

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