Nordsjællands Hospital
Hillerød, 3400, Denmark
NCT Number: NCT03679130
A physically active lifestyle during pregnancy has potential to improve maternal and child health. However, less than four out of ten Danish pregnant women succeed to achieve 30 minutes of daily physical activity at moderate intensity as recommended by the Danish Health Authorities. This project investigates how to implement physical activity in pregnant women´s everyday life by testing the efficacy of two very different exercise programs on physical activity level during pregnancy.
Looking for future studies?
Notify Me18 year and older
Female
Interventional
Not applicable
Hillerød, 3400, Denmark
Low levels of physical activity during pregnancy constitute a significant public health issue as increasing evidence suggests that the mother's lifestyle during pregnancy may influence the future health of her child. A physically active lifestyle during pregnancy has potential to improve metabolic health of mother and child and thus may play an important role in relation to counteracting the obesity epidemic and the increasing incidence of metabolic diseases that escalates globally.
However, less than four out of ten Danish pregnant women succeed to achieve 30 minutes of daily physical activity at moderate intensity as recommended by the Danish Health Authorities. The key gap in evidence and practice towards tackling the significant public health issue of being physically inactive during pregnancy is lack of evidence of how physical activity can be implemented. Only very few and scattered regional or municipal physical activity initiatives are currently targeting Danish pregnant women, and these are mainly targeted overweight women. Implementing and validating means to empower the pregnant women to be physically active have the potential to establish the norm of being physically active during pregnancy and might halt the negative spiral effect of physical inactivity, obesity and metabolic diseases that escalates globally.
The aim of FitMum RCT is to evaluate the effects of structured supervised exercise training and motivational counseling supported by health technology on physical activity level during pregnancy. The two exercise programs are designed to meet the motivators and overcome the specific barriers for physical activity among pregnant women. The programs will be tested in a three-armed randomized controlled trial including 220 healthy, physically inactive, pregnant women.
FitMum is carried out in collaboration between University of Copenhagen, Nordsjaellands Hospital, Technical University of Denmark, Aarhus University and international researchers.
During the COVID-19 pandemic supplies of interventions and test visits are periodically changed. During lockdown periods, all interventions and test visits (except delivery) are converted into online versions. In EXE, the water exercise sessions are replaced with online land exercises. All land exercise sessions consist of 30 min of aerobic exercise where the participants exercise on their own followed by 30 min of supervised online group resistance training. All individual and group MOT sessions are held online. As much data as possible is collected during the pandemic, but in some periods, biological samples and DXA scans have been cancelled and participants were weighed at home.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
EXE contains three weekly one-hour exercise sessions at moderate intensity, more specifically one water exercise session and two land exercise sessions. The training will be supervised, held in teams, and both water and land exercise sessions will consist of a combination of aerobic and resistance training.
Other names: EXE
MOT contains four individual and three group counseling sessions taking place from randomization until GA week 33+6 and aim to motivate the participants to increase their physical activity level at moderate intensity. During individual sessions, feedback on physical activity performance will be provided based on activity data acquired from the activity tracker and further, MOT-participants will receive weekly SMS-reminders about physical activity.
Other names: MOT
Time frame: Continuously 24/7 from inclusion (at latest GA week 15+0) to GA week 28+0-6
Physical activity level from randomization to GA week 28+0-6 determined by a wrist-worn activity tracker, Garmin Vivosport, with built-in heart rate monitor and accelerometer. The activity tracker is to be worn continuously by the women from inclusion until delivery. After inclusion baseline physical activity level will be measured for one week, followed by randomization to one of the three study groups and continuous monitoring of physical activity level by the activity tracker. Preferably, the activity tracker is also worn continuously from delivery and one year ahead. The activity tracker determines the frequency, duration and intensity of activity periods on a minute-to-minute basis and data from the activity tracker is wirelessly synced to its associated smartphone application, Garmin Connect, and research platform, Fitabase.
Time frame: Baseline weight, weight at inclusion, weight at GA week 28+0-6, weight at GA 34+0-6 and weight at delivery.
Weight gain during pregnancy
Time frame: At inclusion, GA week 28+0-6 and 34+0-6
A Danish version of the validated 'Pregnancy Physical Activity Questionnaire' (PPAQ-DK) will be used to subjectively measure physical activity level during pregnancy.
Time frame: At GA week 28+0-6
The doubly labeled water technique will be used to measure free-living energy expenditure at GA week 28+0-6.
Time frame: Continuously 24/7 from inclusion to delivery
The activity tracker will also be used to measure physical activity level of the mother during the entire pregnancy period, meaning after GA week 28+0-6 until delivery as well.
Time frame: Continuously 24/7 from delivery and one year ahead
The activity tracker will also be used to measure physical activity level of the mother one year after delivery.
Time frame: Delivery
Clinical pregnancy, delivery and neonatal outcomes will be collected from medical records. E.g. incidence of Gestational Diabetes Mellitus, gestational age at delivery, mode of delivery, induction of labor, epidural, 5-minute Apgar score, pH of umbilical cord and birth weight.
Time frame: At GA week 28+0-6
Maternal body composition will be assessed by doubly labeled water during pregnancy.
Time frame: One week after delivery
Maternal body composition will be assessed by DXA scanning after delivery.
Time frame: At inclusion, GA week 28+0-6, 34+0-6, and one year after delivery
Health-related quality of life and function will be determined by a Danish version of the questionnaire "Medical Outcomes Study Short Form 36" (SF-36).
Time frame: At inclusion, GA week 28+0-6, and 34+0-6
Sick leave and pelvic and low back pain will be assessed by a questionnaire verbally administered at interviews at visits.
Time frame: Continuously 24/7 from inclusion (at latest GA week 15+0) to 1 year after delivery
Sleep quantity and quality will be assessed continuously by the activity tracker.
Time frame: At inclusion, GA week 28+0-6, GA week 34+0-6 and one year after delivery
Sleep quantity and quality will be assessed by a Danish version of the questionnaire "Pittsburgh Sleep Quality Index" (PSQI).
Time frame: At inclusion, GA week 28+0-6, 34+0-6, and delivery
Plasma metabolites and hormones (e.g. triglyceride, HDL, LDL, total cholesterol and HbA1C) will be assessed by analysing maternal blood and umbilical cord blood.
Time frame: At GA week 34+0-6 and delivery.
Epigenetic profiles will be assessed by analysing DNA methylation in maternal blood, paternal blood and umbilical cord blood.
Time frame: At delivery
Placental function will be assessed via analyses of placental samples, maternal blood and umbilical cord blood.
Time frame: From inclusion (at latest GA week 15+0) to delivery
Investigations of personal understandings of physical activity in everyday life of pregnant women and social, structural and cultural practices and factors influencing successful implementation of exercise during pregnancy will be based on semi-structured qualitative interviews
Time frame: From inclusion (at latest GA week 15+0) to delivery
Investigations of personal understandings of physical activity in everyday life of pregnant women and social, structural and cultural practices and factors influencing successful implementation of exercise during pregnancy. Data will be collected by observations
Time frame: From inclusion (at latest GA week 15+0) to delivery
Investigations of personal understandings of physical activity in everyday life of pregnant women and social, structural and cultural practices and factors influencing successful implementation of exercise during pregnancy. Data will be collected by auto-documentation.
Time frame: From inclusion (at latest GA week 15+0) to delivery
Mixed methods will be used to do a qualitative and quantitative process evaluation. Data for the process evaluation are based on semi-structured qualitative interviews and administratively collected process data (e.g. frequency of training and counseling sessions, visits and measurements), electronic case report form files, and activity logs.
Time frame: At inclusion, GA week 28+0-6, GA week 34+0-6 and one year after delivery
Self-efficacy for physical activity will be measured by a Danish version of the American questionnaire "Pregnancy Exercise Self-efficacy Scale" (P-ESES-DK).
Time frame: At inclusion, GA week 28+0-6, GA week 34+0-6 and one year after delivery
Motivation for physical activity will be measured by a Danish version of the British questionnaire "Behavioral Regulation Exercise Questionnaire" (BREQ-2).
Time frame: At 5 weeks, 5 months and 12 moths after delivery
Growth in the offspring will be assessed by questionnaires, using data from visits to the participants' general practitioners.
Time frame: One year after due date
Physical psycho-motor development in the offspring will be assessed using a Danish version of the questionnaires Ages and Stages 3 (ASQ-3) for 12- and 14 month old babies.
Time frame: One year after due date until one year and 7 days after due date
Physical activity level one year after due date, determined by a wrist-worn accelerometer, Actigraph GT3X+. The activity tracker is to be worn continuously by offspring for 7 days. Data is stored in the device and transferred to the researchers' computer.
Time frame: 6 weeks after delivery
Mental well-being in mothers and fathers post partum will be assessed using a Danish validated screening-tool for parental post-partum depression, primarily based on the Edinburgh Postnatal Depression Scale and selected questions from The Masculine Depression Scale.
Time frame: For one night, between GA week 28+0 until delivery
validation of activity trackers for measuring sleep will be conducted using polysomnography (PSG) in a sub-group of forty women already participating in FitMum RCT. The women will wear the PGS for one night.
Time frame: 7-14 days after delivery
Breastmilk for metabolomics and lipidomics analyses is obtained from one single feed 7-14 days after delivery.
Nordsjaellands Hospital
Other
Acronym: FitMum-RCT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03489564
Behavior, Motor Activity
Baton Rouge, Louisiana, United States
View Trial DetailsNCT03271723
Behavior, Breast Feeding
Pelotas, Rio Grande do Sul, Brazil
View Trial DetailsNCT01364506
Behavior, Motor Activity
Botucatu, São Paulo, Brazil
View Trial DetailsNCT06750406
Anxiety Disorders, Behavior
Lahore, Punjab Province, Pakistan
View Trial Details