Singleton Hospital, Maternity Unit
Swansea, SA2 8QA, United Kingdom
NCT Number: NCT03748888
The main theme of this study focuses on providing evidence of the impact of antenatal physical activity on maternal/foetal cardiovascular changes during pregnancy and maternal cardiovascular adaptations during the early postpartum period.
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Notify Me18 year–40 year
Female
Interventional
Not applicable
Swansea, SA2 8QA, United Kingdom
Overwhelming research supports the general benefit of antenatal physical activity (APA) for pregnant women, but there is a lack of knowledge about the influence of exercise on cardiovascular physiology in healthy and overweight pregnant women and their foetuses. Also some research supports the theory of foetal programming; which establish that maternal habits during pregnancy will impact in-utero environment, so if this maternal habits are healthy ones they could improve foetal health.
Cardio vascular disease (CVD) was the top cause of death all over the world in 2015. In Wales CVD as cause of death is still one of the top ones. However, these statistics could be improved if people adopt healthier lifestyle habits, since 54% and 45% of Welsh women are overweight/obese or sedentary respectively. Pregnancy seems to be a teachable moment for women and the starting point of adopting healthy life-style habits. Therefore, by introducing Welsh pregnant women to exercise, there is the potential to improve their health and of their foetuses an also exert an exponential impact on future generations.
The main theme of this study focuses on providing evidence of the impact of APA on maternal/foetal cardiovascular changes during pregnancy and maternal cardiovascular adaptations during the early postpartum period.
This is a 3-year study carried out in Swansea University, Singleton Hospital.
The project leading to this application has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 663830.
Healthy pregnant women with no contraindications for exercise will be eligible for the study and those who want to participate in the project will be allocated into an exercise group (EG) or a control group (CG). EG participants will receive an intervention based on an APA during 20-24weeks, CG participants will follow their standard health care during pregnancy.
All participants must attend three cardiovascular assessment protocols (18-22 weeks & 32-36weeks during pregnancy, 12weeks postpartum). These protocols will involve maternal/foetal electrocardiograph and echocardiograph evaluation, heart-rate monitoring and moderate physical exercise (walking).
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
An antenatal physical activity (APA) programme will be designed for participants in the exercise group.
The APA will last for 20-24 weeks. Participants in the EG must enrol in the APA between their 12-16 weeks of gestation.
The APA programme has a frequency of three times a week, which involves aerobic, strength and stretching exercises. The intensity of the APA programme is individually calculated for each participant based on their pre-pregnancy fitness level. Single sessions of the APA programme last 50-60min.
Time frame: 18 and 36 weeks of gestation, 12 weeks postpartum.
Maternal cardiac output at rest, during exercise and after exercise measured in L/min would be recorded from study participants to analyse and compare potential changes inter and intra group.
Time frame: 18 and 36 weeks of gestation, 12 weeks postpartum.
Maternal heart rate at rest and after exercise would be recorded in beats per minute to be analysed and compared inter and intra group.
Time frame: 18 and 36 weeks of gestation, 12 weeks postpartum.
Maternal heart rate variability at rest, during and after exercise would be measured by r to r interval. It would be recorded and analysed to compare inter and intra group changes.
Time frame: 36 weeks pregnancy
Foetal heart rate baseline would be measured at rest, during and after exercise. It would be analysed and compared in between groups.
Time frame: 18 and 36 weeks pregnancy.
Data obtained from accelerometer devices worn by exercise group participants.
Time frame: 18 and 36 weeks pregnancy.
Data obtained from accelerometer devices worn by control group participants.
Time frame: 12 weeks postpartum.
Data obtained from accelerometer devices worn by all participants in the study.
Time frame: 36 weeks pregnancy.
Weight gain during pregnancy measured in kilograms would be recorded to be compared in between study groups.
Time frame: 18 and 36 weeks pregnancy.
Body fat percentage calculated from skinfold-thickness measures would be compared in between study groups.
Time frame: Second week after birth.
Birth weight from new borns recorded in kilograms would be collected from maternal records. It would be analysed and compared between groups.
Time frame: 18 and 36 weeks pregnancy.
The Qol-Grav questionnaire is a validated questionnaire used to measure quality of life in pregnant women. This questionnaire would be filled in by study participants and analysed to record their quality of life during the current pregnancy. Scores derived from the questionnaire would be analysed and compared between groups.
The following total score scale is presented:
9-18: Excellent quality of life. 19-27: Very good quality of life. 28-36: Good quality of life. 37-45: Not very good quality of life.
Time frame: 12 weeks pregnancy.
Participants' pre-pregnancy physical activity levels would be registered using the modified physical activity questionnaire. This questionnaire records information about activities performed for the three months before pregnancy. Intensity of the activity would be recorded using three different levels of intensity (low, moderate and vigorous). Average time spent in each activity would be recorded in minutes. These values would be used to measure time and intensity spent in physical activity before pregnancy, and would be compared between groups.
Time frame: 12 weeks pregnancy.
Participants' physical activity levels during the first trimester of pregnancy would be registered using the modified physical activity questionnaire. This questionnaire records information about activities performed during the first three months of pregnancy. Intensity of the activity would be recorded using three different levels of intensity (low, moderate and vigorous). Average time spent in each activity would be recorded in minutes. These values would be used to measure time and intensity spent in physical activity during pregnancy, and would be compared between groups.
Time frame: 36 weeks pregnancy.
Participants' physical activity levels during the second and third trimester of pregnancy would be registered using the modified physical activity questionnaire. This questionnaire records information about activities performed during the second an third trimesters of pregnancy. Intensity of the activity would be recorded using three different levels of intensity (low, moderate and vigorous). Average time spent in each activity would be recorded in minutes. These values would be used to measure time and intensity spent in physical activity during pregnancy, and would be compared between groups.
Time frame: 18 and 36 weeks of pregnancy.
Two questionnaires would be used to measure participants' quality of sleep during their pregnancy. These questionnaires are the Pittsburgh Sleep Quality Index and the Insomnia Severity Index.
Time frame: 12 weeks postpartum.
Two questionnaires would be used to measure participants' quality of sleep during the postpartum period. These questionnaires are the Pittsburgh Sleep Quality Index and the Insomnia Severity Index.
Time frame: 12 weeks postpartum.
The Brief Screening Questionnaire for Infant Sleep Problems would be used to register sleep patterns in the three months old infants born from study participants. Items recorded in the questionnaire are the following: sleep arrangement, time spent sleeping during the day and night, number of wakings per night, mode of falling asleep, time spent in wakefulness and normal time of falling asleep at night.
Time frame: 2 weeks postpartum.
Type of delivery such as vaginal, cesarean section or instrumental birth would be recorded from maternal records after birth.
Time frame: 2 weeks postpartum.
Type of analgesia (pharmacological or non-pharmacological) used during labour would be recorded from maternal records after birth.
Time frame: 2 weeks postpartum.
Apgar score is a scale that measures health in the new born. This scale focuses on five parameters (skin colour, heart rate, reflexes and responsivness, muscular tone, and breathing rate), each of them rated from 0 to 2. This test is performed at the first and fifth minute of new born's life. Scores above 7 are consider normal, scores below 7 indicates that the new born needs medical attention. Scores from both tests (1min and 5min) would be recorded from maternal records after birth.
Time frame: 18 and 36 weeks of pregnancy.
Maternal hand grip strength would be measured using a hand grip dynamometer. This test would be performed during the second and third trimester of pregnancy.
Time frame: 12 weeks postpartum.
Maternal hand grip strength would be measured using a hand grip dynamometer. This test would be performed during the postpartum period.
Time frame: 18 and 36 weeks of pregnancy.
Maternal upper body flexibility during second and third trimester would be measured using the back scratch test. This test measures how close the hands can be brought together behind the back.
Time frame: 12 weeks postpartum.
Maternal upper body flexibility during the early postpartum would be measured using the back scratch test. This test measures how close the hands can be brought together behind the back.
Swansea University
Other
Physical Exercise, Cardiovascular Adaptation Monitoring in Pregnancy
Acronym: PE-CAMP
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