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Maternal Loss of Control Eating

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03269253
Enrollment
14451
Registered
2017-08-31
Start date
2016-08-01
Completion date
2017-07-20
Last updated
2017-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eating Disorder, Obesity

Keywords

ALSPAC, longitudinal

Brief 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).

Detailed 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.

Interventions

None listed

Sponsors

Icahn School of Medicine at Mount Sinai
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 43 Years
Healthy volunteers
No

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;

Design outcomes

Primary

MeasureTime frameDescription
birth weightDay 1weight at birth

Secondary

MeasureTime frameDescription
BMIaverage 21 yearsbody mass index
Food Frequency Questionnaire (FFQ)average 9 monthsadult dietary patterns - software specific to the FFQ will be used to analyze data.
Food Frequency Questionnaireaverage 21 yearschild dietary patterns- software specific to the FFQ will be used to analyze data.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026