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Post-delivery Maternal-offspring Obesity and Metabolic Risk After a Prepregnancy Weight-loss Intervention (PrepareD)

Kaiser Permanente logo

Kaiser Permanente

Status

Completed

Conditions

Obese
Overweight
Metabolic Disorders
Postpartum

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT06067126
5R01DK125348 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of PrepareD is to examine whether the prepregnancy weight-loss intervention administered during the Prepare trial [NCT02346162] has an influence in the postnatal period. PrepareD is a cohort study (no intervention) that will address new specific aims through one in-person visit with mothers and children, dietary recalls, actigraphy, and the use of medical record weights. The goal is to collect data when the child is 3 years old. However, due to the COVID-19 pandemic, the investigators expanded the data collection window in order to collect data up to when the child is 5 years old. The investigators hypothesize that intervening on women before pregnancy is the key to breaking the multigenerational cycle of obesity.

Enrollment

154 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Mother must be a Prepare [NCT02346162] participant who has experienced a viable pregnancy during the Prepare trial
  • Child must be the first viable offspring born to a Prepare participant after consent into the Prepare study

Exclusion Criteria: None

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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