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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02180152
Other study ID # Caminhadas2014
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date March 2015
Est. completion date March 2016

Study information

Verified date July 2020
Source Professor Fernando Figueira Integral Medicine Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility 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.

Study Design


Intervention

Behavioral:
Postprandial walks
Obese pregnant women will be target to carry out walks lasting 10' after the main meals (breakfast, lunch and dinner), Monday to Friday, during 8 weeks. Adherence to the program will be determined by daily readings of pedometers previously provided to pregnant women; minimum of 1500 steps per day from Monday to Friday.

Locations

Country Name City State
Brazil Instituto de Medicina Integral Professor Fernando Figueira Recife Pernambuco

Sponsors (1)

Lead Sponsor Collaborator
Professor Fernando Figueira Integral Medicine Institute

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight gain after postprandial walks in obese pregnant women. 8 weeks
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