Maternal Loss of Control Eating

Obesity Clinical Trial

Official title:

Maternal Loss of Control Eating: a Longitudinal Study of Maternal and Child Outcomes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03269253
• Other study ID #: GCO 15-1668
• Status: Completed
• Phase: N/A
• First received: August 29, 2017
• Last updated: August 29, 2017
• Start date: August 1, 2016
• Est. completion date: July 20, 2017

Study information

• Verified date: August 2017
• Source: Icahn School of Medicine at Mount Sinai
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study focused on investigating the effects of maternal disordered eating on maternal and child outcomes as part of a secondary data analysis of the Avon Longitudinal Study of Parents and Children (ALSPAC).

Description:

Deidentified and anonymised data already collected as part of the ALSPAC study will be analysed to investigate the effects of maternal eating on maternal and child outcomes (diet, eating, weight, metabolic). The Avon Longitudinal Study of Parents and Children (ALSPAC) is a longitudinal, prospective study designed to examine the effects of environment, genetics and other factors on health and development.All pregnant women living in the geographical area of Avon, UK, who were expected to deliver their baby between 1st April 1991 and 31st December 1992, were recruited. 14,541 women were enrolled. Amongst these pregnancies, there were a total of 14,676 fetuses, resulting in 14,062 live births and 13,798 children who were alive at 1 year of age and were singletons. The ALSPAC study website contains details of all the data that is available through a fully searchable data Dictionary (http://www.bris.ac.uk/alspac/researchers/data-access/data-dictionary/).

Missingness will be assessed and standard data analytical techniques such as MI will be used.Crude and adjusted logistic, linear, and multinomial regression models will be employed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 14451
• Est. completion date: July 20, 2017
• Est. primary completion date: July 20, 2017
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 16 Years to 43 Years

Eligibility

Inclusion Criteria:

Exclusion Criteria:

• multiple pregnancies

• no questionnaire data at 32 weeks.

eligibility criteria : enrolled in the ALSPAC study; inclusion: all women part of the ALSPAC study;

Related Conditions & MeSH terms

• Eating Disorder
• Feeding and Eating Disorders
• Obesity

Locations

Country	Name	City	State
United States	Icahn School of Medicine at Mount Sinai	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Icahn School of Medicine at Mount Sinai

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	birth weight	weight at birth	Day 1
Secondary	BMI	body mass index	average 21 years
Secondary	Food Frequency Questionnaire (FFQ)	adult dietary patterns - software specific to the FFQ will be used to analyze data.	average 9 months
Secondary	Food Frequency Questionnaire	child dietary patterns- software specific to the FFQ will be used to analyze data.	average 21 years