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Study of Antenatal Care Intervention Directed to Pregnant Women With Obesity

Mighty Mums - a Lifestyle Intervention at Primary Care Level for Pregnant Women With Obesity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03147079
Acronym
Mighty Mums
Enrollment
1354
Registered
2017-05-10
Start date
2011-01-01
Completion date
2017-12-31
Last updated
2025-04-04

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

Conditions

Obesity Complicating Childbirth

Keywords

obesity, pregnancy, lifestyle, gestational weight gain, weight of offspring, antenatal care, health behavior, physical activity, diet, programme evaluation, costs and costs analysis

Brief summary

The purpose of this study is to determine whether a behavioural intervention focusing on diet and physical activity is cost-effective in decreasing weight gain during pregnancy among pregnant women with body mass index above 30, and has effect on the weight of offspring at birth and at 2.5 years of age

Detailed description

Obesity in relation to pregnancy is becoming an increasing public health issue and 48% of women assigned to antenatal care in Sweden have overweight (BMI≥25) or obesity (BMI≥30). Obesity is associated with adverse perinatal outcomes, the risks increase with increasing BMI and excessive gestational weight gain (GWG) further increases the risks of adverse pregnancy outcomes. Lifestyle intervention can help pregnant women with obesity to limit their GWG. This study evaluated whether a low-budget antenatal lifestyle intervention programme, with emphasis on nutrition and physical activity, influenced GWG and maternal and perinatal outcomes for pregnant women with obesity. The study also evaluated which specific components of the intervention that had effect.

Interventions

BEHAVIORALLifestyle intervention

Sponsors

Vastra Gotaland Region
CollaboratorOTHER_GOV
Göteborg University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Open intervention study with 2 control arms

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* pregnant * BMI\>30

Exclusion criteria

* first antenatal care visit after week 20 of the pregnancy * abortion * miscarriage

Design outcomes

Primary

MeasureTime frameDescription
Gestational weight gain < 7 kg7 monthsWeight gain measured from enrollment/first antenatal care visit to last visit before partum, measured in kg

Countries

Sweden

Outcome results

None listed

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