Weight stigma in pregnancy: a hidden risk?
NCT ID NCT06531694
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will follow 800 pregnant women to see if weight stigma and discrimination contribute to complications like gestational diabetes. Researchers will also examine psychological factors such as trauma and eating disorders. The goal is to better understand the link between body size and pregnancy outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could highlight weight stigma as a key factor in pregnancy complications, leading to better support and interventions for expectant mothers.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. Results may be influenced by unmeasured factors, and findings may not apply to all populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 800 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Jun 2026
An estimate. Start dates often move.
- Expected to finish
-
Dec 2028
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants will be pregnant women who are at least 18 years old with a singleton pregnancy, and who are booked in to give birth at Adelaide Women's and Children's Hospital or Royal Women's and Children's Brisbane. At baseline, women must be between 10 and 22 weeks' gestation.
- Ages
-
18 years and older
- Sex
-
Female participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Pregnant between 10-22 weeks' gestation * Greater or equal than 18 years of age * Booked to give birth at Adelaide Women's and Children's Hospital or Royal Women's and Children's Brisbane * Access to the Internet to complete the survey * Consents to the extraction of hospital electronic medical record data about the woman and relevant to the study. * Ability to read and understand English Exclusion Criteria: * Pregnant with multiple gestation * Insufficient English language skills to consent and complete the questionnaires.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Overweight and obesity are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can diet and exercise in pregnancy shape a Child's health for years?
- Gut microbes in pregnancy and infancy: a window into lifelong health?
- Can cottonseed oil improve cholesterol? trial tests common cooking oil against similar blends
- Can Weight-Loss surgery weaken protein digestion in older adults?
- Can pole walking boost heart fitness in diabetic patients?
- Weight loss after cancer: a new program aims to help survivors