Impact of a Nutritional Intervention Program for Weight Control During Pregnancy

Federal University of Health Science of Porto Alegre

Status: Completed

Conditions: Pregnancy Complications; Weight Gain

Treatments: Behavioral: Dietary Advice

Study type: Interventional

Funder types: Other

Identifiers

NCT00634530

vitolo4

Details and patient eligibility

About

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.

Enrollment: 318 patients

Sex: Female

Ages: Under 35 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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318 participants in 1 patient group

I, Intervention

Other group

Treatment:

Behavioral: Dietary Advice