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Weighing In Pregnancy

In antenatal women, does weighing at each visit compared with routine antenatal care reduce the incidence of excessive weight gain during pregnancy?

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000331033
Acronym
WIP
Enrollment
782
Registered
2010-04-23
Start date
2010-01-01
Completion date
2012-11-30
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

Overweight and obesity are the most common clinical risk factors affecting over 30% of the pregnancy population. Furthermore, excessive weight gain while pregnant also leads to increased morbidity and mortality for the woman and the fetus/neonate. The morbidity includes, for the fetus/neonate: macrosomia, shoulder dystocia, hypoglycemia and admission to the nursery and for the mother: high blood pressure, gestational diabetes, increased caesarean section rates and increased rates of overweight and obesity post pregnancy. A number of studies have targeted diet and exercise with varied effect. No study has focused on routinely weighing patients in clinic to provide regular feedback that may act as a positive behavioural component to limit weight gain. This study will investigate the effect of weighing pregnant patients at each antenatal clinic visit compared with routine care (weight recorded at the booking visit). All patients attending the Royal Women’s Hospital for their booking visit (<20weeks gestation) will be approached by a midwife or doctor. Only women planning to have all their antenatal care at the Royal Women's Hospital, and with no obvious medical problems, will be included. Once consented, patients will then be randomised into either the control or the intervention groups. Patients in the intervention group will be weighed at every antenatal visit until 36-38 weeks gestation, while the control group will receive routine care with a booking weight plus a weight at 36-38 weeks gestation. Information will be obtained about their demographics, previous pregnancies, medical problems and delivery. Participants will complete a questionnaire at the end of the study regarding their perception of being weighed. We will then analyse the mean pregnancy weight gain of the intervention group compared to the control group. We will also analyse the data according to the Body Mass Index (BMI) at entry to determine if particular subgroups of women (ie underweight, normal weight, overweight and obese) appear to have a different response to being weighed. We will also compare the neonatal outcomes to ensure there is no obvious harm in the process of regular weighing. This study will allow us to determine if weighing patients regularly does provide a positive behavioural component resulting in appropriate weight gain in pregnancy.

Interventions

weighing will be included in the routine antenatal check at each visit. The number and length of the antenatal visits will remain routine ie 10 visits in the pregnancy at 15 to 30minute consults.

Sponsors

Fiona Brownfoot
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

Pregnant women at < 20 weeks gestation.

Exclusion criteria

Multiple gestation Extremes of reproductive age (<18 or >45years) Medical complicating factors at booking (including thyroid disease, diabetes (type 1 or 2), psychiatric illness etc) Substance abuse First antenatal visit >20weeks gestation Intention to complete antenatal care through another clinic Intention to have shared care Unable to understand English

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026