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Vitamin D During Pregnancy

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01589783
First Posted: May 2, 2012
Last Update Posted: July 28, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Hadassah Medical Organization
  Purpose
Vitamin D insufficiency is common globally. Pregnant women, who need an increased supply of this vitamin for the proper development of the fetus, are a significant risk group. The purpose of this study is to examine which factors - education, knowledge from non-professional sources, recommendations from medical staff - influence the use of vitamin D among pregnant women in light of the lack of a clear health policy, and to help formulating guidelines for a new health policy with specific recommendations for vitamin D dosage in pregnancy.

Condition Intervention
Vitamin D Deficiency Other: completion of a questionnaire Other: Blood draw

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Evaluation of the Influence of Education, Knowledge and Existing Guidelines on the Consumption of Vitamin D During Pregnancy.

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

Primary Outcome Measures:
  • Use of Vitamin D in Pregnant Women [ Time Frame: 3 months ]

Enrollment: 764
Study Start Date: May 2012
Study Completion Date: June 2015
Primary Completion Date: June 2014 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Pregnant or newly post partum women Other: completion of a questionnaire
Completion of a questionnaire
Other: Blood draw
A subset of 100 women will have a blood test to measure Vitamin D levels
family practice physicians and obstetricians Other: completion of a questionnaire
Completion of a questionnaire

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 50 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
We are recruiting either pregnant women or those who just gave birth (and still hospitalized) and a group of both family practice physicians and obstertricians.
Criteria

Inclusion Criteria for the pregnant of newly post-partum women:

  • women between 18-50
  • pregnant or just given birth and still hospitalized
  • understand and can read Hebrew

Exclusion Criteria:

  • those who do not understand or read Hebrew
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01589783


Locations
Israel
Hadassah Medical Organization
Jerusalem, Israel
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Drorith Hochner, MD Hadassah Medical Organization
  More Information

Responsible Party: Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT01589783     History of Changes
Other Study ID Numbers: VitDand Preg-HMO-CTIL
First Submitted: April 1, 2012
First Posted: May 2, 2012
Last Update Posted: July 28, 2015
Last Verified: July 2015

Keywords provided by Hadassah Medical Organization:
Pregnancy
Vitamin D

Additional relevant MeSH terms:
Vitamin D Deficiency
Avitaminosis
Deficiency Diseases
Malnutrition
Nutrition Disorders
Vitamins
Vitamin D
Ergocalciferols
Micronutrients
Growth Substances
Physiological Effects of Drugs
Bone Density Conservation Agents