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Aerobic Training in Pregnant Women With Gestational Diabetes and Chronic Hypertension

Aerobic Training Effect in Pregnant Women With Gestational Diabetes and Chronic Hypertension: Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01885234
Enrollment
9
Registered
2013-06-24
Start date
2011-12-31
Completion date
2015-12-31
Last updated
2015-12-22

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

Conditions

Chronic Hypertension in Obstetric Context, Gestational Diabetes Mellitus, Pregnancy

Keywords

Glycated hemoglobin, HOMA, Pregnancy, aerobic exercise

Brief summary

The aim of the present study is verify glycated hemoglobin (HbA1c) and HOMA behavior in pregnant women with gestational diabetes or chronic hypertension after an aerobic training in cycle-ergometer. The sample is composed by 64 pregnant and sedentary women, 20 weeks' pregnant. Two experimental groups (gestational diabetes and chronic hypertension, n = 16 each) will perform a low-intensity aerobic training in cycle-ergometer, three times/week, for 45 minutes each session. Two control groups (gestational diabetes and chronic hypertension, n = 16 each) will perform an unique session/week of relaxation and stretching. Outcomes: first ventilatory threshold, HbA1c,HOMA, type of delivery, weight and height of the newborn.

Detailed description

The statistical analysis will consist of: * descriptive statistic; * Levene's test * Shapiro Wilk's normality test * Parametric or non-parametric test * a=0.05 * SPSS 17.0

Interventions

OTHERAerobic exercise

Pregnant women with Gestational Diabetes and pregnant women with chronic hypertension will perform 50 minutes of aerobic exercise in a bicycle, 3 times a week

Pregnant women with Gestational Diabetes and pregnant women with chronic hypertension will perform 50 minutes of stretch exercise, once a week

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
20 Weeks to 27 Weeks
Healthy volunteers
Yes

Inclusion criteria

* age \> 20 years; * gestational age between 20 and 27 weeks (date of the last period and confirmed by ultrasound); * Only one foetus in the womb; * Without orthopedic limitations; * Non-smoker; * Medical clearance for exercise

Exclusion criteria

* Pre-eclampsia; * fetal malformations; * Intrauterine fetal death

Design outcomes

Primary

MeasureTime frame
glycated hemoglobinday 1 and 10 weeks after training

Secondary

MeasureTime frame
HOMAday 1 and 10 weeks after training

Other

MeasureTime frame
First ventilatory thresholdday 1 and 10 weeks after training

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026