Resistance Exercise Training During Pregnancy: a Randomized Controlled Trial

NCT ID: NCT00813657

Last Updated: 2008-12-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2000-01-31

Study Completion Date

2002-03-31

Brief Summary

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The investigators investigated the effects of a supervised maternal exercise training program (performed during the 2nd and 3rd trimesters of pregnancy) on maternal-newborn unit health outcomes in a group of previously sedentary healthy women. A matched control group was assessed over the same time period. Given the fact that most studies in the field have used aerobic exercises, here the investigators largely focused on very light resistance, toning exercises.

Detailed Description

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Conditions

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Gestational Age Birth Weight Anaemia Gestational Diabetes Mellitus Type of Delivery

Study Design

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Allocation Method

RANDOMIZED

Primary Study Purpose

PREVENTION

Study Groups

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Lifestyle counseling

Group Type EXPERIMENTAL

Exercise

Intervention Type BEHAVIORAL

Women in the intervention group were enrolled in three sessions/week of individually supervised, resistance exercise training performed over the second and third trimester of pregnancy (in total 26 weeks, \~80 training sessions). Heart rate (HR) was carefully and individually controlled (≤80% of age-predicted maximum HR value, 220-age) through a heart rate monitor during the training sessions. In brief, each session consisted of 35-40 minutes of exercise divided in a light intensity (≤60% maximal heart rate) warm-up period (\~8 minutes), followed by toning and very light resistance exercises (\~20 minutes) and a light intensity cool-down (\~8 minutes) period. Resistance exercises were performed with barbells (≤3kg per exercise) or low-to-medium resistance bands (Therabands).

Interventions

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Exercise

Women in the intervention group were enrolled in three sessions/week of individually supervised, resistance exercise training performed over the second and third trimester of pregnancy (in total 26 weeks, \~80 training sessions). Heart rate (HR) was carefully and individually controlled (≤80% of age-predicted maximum HR value, 220-age) through a heart rate monitor during the training sessions. In brief, each session consisted of 35-40 minutes of exercise divided in a light intensity (≤60% maximal heart rate) warm-up period (\~8 minutes), followed by toning and very light resistance exercises (\~20 minutes) and a light intensity cool-down (\~8 minutes) period. Resistance exercises were performed with barbells (≤3kg per exercise) or low-to-medium resistance bands (Therabands).

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* sedentary (not exercising \>20 minutes on \>3 days per week)
* with singleton
* not at high risk for preterm delivery (no more than one previous preterm deliveries)
* women planning to give birth in the same obstetrics hospital department (Hospital Severo Ochoa, Madrid, Spain)

Exclusion Criteria

* not being under medical follow-up throughout the entire pregnancy period were not included in the study
* women having serious medical condition that prevent them from exercising safely
Minimum Eligible Age

25 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Universidad Politecnica de Madrid

OTHER

Sponsor Role lead

Responsible Party

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Facultad de Ciencias de la Actividad Física y del Deporte - INEF, Universidad Politécnica de Madrid, Madrid, Spain

Other Identifiers

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01562

Identifier Type: -

Identifier Source: secondary_id

01562

Identifier Type: -

Identifier Source: org_study_id