- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01412580
In Utero Capacity Formation and Socio-economic Outcomes (CDS)
August 5, 2019 updated by: Plamen Nikolov, Harvard University
The Contribution of Health in Utero to Capacity Formation, Education and Economic Outcomes: Experimental Evidence From Tanzania
Because of the high returns of schooling in developing countries, policymakers pay a lot of attention to increasing school access.
But if the mother is deficient in key micronutrients, brain development can biologically constrain children's demand for education.
To execute this strategy, the investigators collect cohort observational data on a previous randomized controlled trial with micronutrient supplements offered to HIV-negative pregnant women in Dar es Salaam, Tanzania, between 2001 to 2003.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This is a cohort study which collected follow-up observational data on households which were offered micronutrient supplements.
The followup study outcomes include various socio-economic household characteristics and parental post-natal behaviors.
Study Type
Observational
Enrollment (Actual)
4000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Dar es Salaam, Tanzania
- MUHAS
-
-
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
18 years to 49 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Individuals from a larger study and this study is an observational follow-up.
Description
These were individuals from the larger study and this study is an observational follow-up.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
observational followup
This was an observational follow-up to a larger study in which treatment group was given 20 mg of vitamin B1, 20 mg of vitamin B2, 25 mg of vitamin B6, 100 mg of niacin, 50 μg of vitamin B12, 500 mg of vitamin C, 30 mg of vitamin E, and 0.8 mg of folic acid
|
observational follow-up
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Children's Cognitive Development
Time Frame: During 2011-2012 (1 year)
|
During 2011-2012 (1 year)
|
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Children's Health
Time Frame: During 2011-2012 (1 year)
|
BMI, Disease Incidence, Self-reported health
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During 2011-2012 (1 year)
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Parental Postnatal Investment Behavior
Time Frame: During 2011-2012 (1 year)
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Outcomes on parental care: care, cognitive stimulation, within-household time and money allocation
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During 2011-2012 (1 year)
|
Educational Status
Time Frame: During 2011-2012 (1 year)
|
School attendance, Student performance (at school), Test Performance
|
During 2011-2012 (1 year)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Parental Labor Force Participation
Time Frame: During 2011-2012 (1 year)
|
Parent's labor force outcomes: labor status, wages, type of job
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During 2011-2012 (1 year)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Plamen Nikolov, Harvard University
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 Major Dates
Study Start
April 1, 2002
Primary Completion (Actual)
September 1, 2012
Study Completion (Actual)
September 1, 2013
Study Registration Dates
First Submitted
August 8, 2011
First Submitted That Met QC Criteria
August 8, 2011
First Posted (Estimate)
August 9, 2011
Study Record Updates
Last Update Posted (Actual)
August 7, 2019
Last Update Submitted That Met QC Criteria
August 5, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- F19899-101
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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