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Postprandial Walking in Obese Pregnant Women and Perinatal Outcomes - a Multicenter Randomized Clinical Trial

P

Professor Fernando Figueira Integral Medicine Institute

Status

Withdrawn

Conditions

Gestational Diabetes
Preeclampsia
Obesity

Treatments

Behavioral: Postprandial walks

Study type

Interventional

Funder types

Other

Identifiers

NCT02180152
Caminhadas2014

Details and patient eligibility

About

The purpose of this study is to verify if postprandial walks are effective in obese pregnant women, as regards to gestational weight gain and typical diseases of that period, as gestational diabetes and preeclampsia. Perinatal outcomes will be observed, such as macrosomia, shoulder dystocia and fetal death.

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 18 and 40 years;
  • Gestational age ≤ 20 weeks, calculated from the last menstrual period and confirmed by the first ultrasound scan;
  • Obesity - body mass index ( BMI ) ≥ 30 kg/m2, based on the weight before pregnancy, reported by pregnant women no more than 5 kg below measured at admission to the study;
  • Physically inactive - according to the International Physical Activity Questionnaire (IPAC);
  • Single pregnancy.

Exclusion criteria

  • Kidney disease or collagen;
  • Previous history of GDM;
  • Diabetes type 1 or type 2;
  • Hypertensive disorders related to pregnancy;
  • Hemodynamic instability;
  • Vaginal bleeding;
  • Visual, auditory or cognitive impairment.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Postprandial walk
Experimental group
Treatment:
Behavioral: Postprandial walks
sedentary pregnant women
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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