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Clinical Trials/NCT00634530
NCT00634530
Completed
Not Applicable

Impact of a Nutritional Intervention Program for Weight Control During Pregnancy

Federal University of Health Science of Porto Alegre1 site in 1 country318 target enrollmentSeptember 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pregnancy Complications
Sponsor
Federal University of Health Science of Porto Alegre
Enrollment
318
Locations
1
Primary Endpoint
Adequated weight gain during pregnancy.
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

This is a randomized clinical trial for evaluate the impact of a nutritional intervention in the weight control of pregnant women according to the nutritional status, and consequently, the reduction of pregnancy complications.

The sample of this study will be composed by 318 pregnant women in the pre-natal care unit of the Health Center in Viamão city / Rio Grande do Sul, including women between the 10th and 25th weeks of gestation, aged up to 35 years old. The eligible pregnant women will be invited by the fieldworks to participated in the trial after be informed about the overall aims of the study. These women willing to participate will be randomly allocated to either the intervention or control group. The intervention group received specific guidelines about feeding practices appropriate to each nutritional status.

Data on pregnant women will be collected through a questionnaire in both groups, and to assess the food intake, three 24-hour food recall will be applied in the interventional group and two recall in the control group, in initial and final gestational period. In all appointments pregnant women of the two groups will be weight and classified according to Body Mass Index of pre-gestational (BMI).

The dietary advices will be elaborated by the author of the project and nutrition graduation students of Federal University of Health Science of Porto Alegre.

Registry
clinicaltrials.gov
Start Date
September 2007
End Date
January 2009
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Federal University of Health Science of Porto Alegre

Eligibility Criteria

Inclusion Criteria

  • Women between the 10th and 25th weeks of gestation
  • To concern in the prenatal care group in basic health unit

Exclusion Criteria

  • Pregnant with diseases that require specific treatment at the onset enrollment (HIV, diabetes, hypertension and anemia)
  • Women 36 years or older.

Outcomes

Primary Outcomes

Adequated weight gain during pregnancy.

Time Frame: one year

Secondary Outcomes

  • Prematurity, low birth weight and pregnancy complications.(one year)

Study Sites (1)

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