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Resistance Exercise Training During Pregnancy: a Randomized Controlled Trial

Effects of Resistance Exercise Training Program Performed During the 2nd and 3rd Trimesters of Pregnancy on Maternal and Newborn Health

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00813657
Enrollment
80
Registered
2008-12-23
Start date
2000-01-31
Completion date
2002-03-31
Last updated
2008-12-23

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

Conditions

Anaemia, Birth Weight, Gestational Age, Gestational Diabetes Mellitus, Type of Delivery

Brief summary

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.

Interventions

BEHAVIORALExercise

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).

Sponsors

Universidad Politecnica de Madrid
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Primary purpose
PREVENTION

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 35 Years
Healthy volunteers
Yes

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

Outcome results

None listed

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