- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00353236
The Contribution of Internal Maternal Resources to Creation of Motherhood. Comparison Among Mothers to Twins and Singleton
July 17, 2006 updated by: Sheba Medical Center
Delivery of twins or preterm infant is a very stressful episode to mothers.
The purpose of this study is to characterize maternal psychological resources in dealing with this situation and compare it to mothers giving birth to singleton at term
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jacob Kuint, MD
- Phone Number: 2227 972-3-5303030
- Email: kuint-j@sheba.health.gov.il
Study Contact Backup
- Name: Liora Findler, PhD
Study Locations
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Ramat -Gan, Israel, 52621
- Recruiting
- Sheba Medical Center - Neonatal Department
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Contact:
- Jacob Kuint, MD
- Phone Number: 2227 972-3-5303030
- Email: kuint-j@sheba.health.gov.il
-
Principal Investigator:
- Jacob Kuint, MD
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 second and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Study group: Mothers who give birth to twins or preterm infants
- Control: Mothers who give birth to singleton, full term infants
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Jacob Kuint, MD, Sheba Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
July 17, 2006
First Submitted That Met QC Criteria
July 17, 2006
First Posted (Estimate)
July 18, 2006
Study Record Updates
Last Update Posted (Estimate)
July 18, 2006
Last Update Submitted That Met QC Criteria
July 17, 2006
Last Verified
July 1, 2006
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SHEBA-06-4170-JK-CTIL
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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