About this trial
Maternal AR has long been used to prevent PTB. However, definitions of AR vary widely, ranging from complete bed rest to partial limitation of physical activity for one or more hours daily.
The use of maternal AR to prevent preterm birth is largely based on observational evidence linking strenuous physical activity to an increased risk of preterm birth, and the assumption that reduced activity may decrease myometrial activity. However, the existing evidence on the clinical effects of AR remains limited and has not demonstrated a reduction in preterm birth or a delay in deliv-ery. In contrast, some studies suggest a potential increase in preterm birth following AR and instead significant adverse maternal and fetal effects.
The overall aim of this study is to compare gestational age at birth in women with a short cervix who are prescribed AR compared with women with a short cervix who are not prescribed AR (NAR).
The primary hypothesis is that NAR is non-inferior to AR in prolonging pregnancy in women with a short cervix.
Secondary hypotheses are that, compared with AR, NAR is associated with higher level of physical activity, lower risk of maternal depression, and reduced risk of loss of maternal bone mineral density.
Through the BEWISE study, we wish to implement a change in the Danish national clinical practice regarding AR from recommending AR in risk groups (current practice) to no longer recommending AR as part as routine care (new practice). We will evaluate this change in clinical practice by prospectively collecting data from women both before and after implementation of the new recommendation. The transition from AR to NAR will be implemented sequentially in each Danish region using a randomised stepped-wedge (SW) cluster design, with each region constituting a cluster. The order in which regions transition is determined by randomisation. Each region will adopt the new recommendation at 3-month intervals, resulting in full national transition from AR to NAR within 12 months Eligible participants are pregnant women in gestational age 20+0 to 33+6 and cervical length \< 25 mm in singleton pregnancies and \< 30 mm in multiple pregnancies. Participants must be above 18 years of age and be able to read and understand Danish or English. There are no exclusion criteria.
The primary outcome is gestational age in days (continuous).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Cervical length < 25 mm in singleton pregnancies and < 30 mm in multiple pregnancies
Above 18 years of age
Reads and understands Danish or English
Disqualifiers
None
Trial design
Sequential
Treatments tested in this trial
Activity Restriction
BehavioralRecommendation to restrict physical activity in pregnant women with a short cervix. This may include increased rest or bed rest according to local clinical practice.
No Activity Restriction
BehavioralRecommendation to continue normal daily activity in pregnant women with a short cervix, without restricting physical activity.
Treatment groups
Trial outcomes
Primary outcomes
Gestational age at birth
Gestational age at birth measured in completed days of pregnancy. This is calculated based on the estimated due date from ultrasound (crown-rump lenght \<14weeks).
Secondary outcomes
Birth before 37 weeks of gestation
Gestational age at birth, pooled
* 14+0-21+6 weeks * 22+0-27+6 weeks * 28+0-31+6 weeks * 32+0-36+6 weeks * Birth after 37+0 weeks of gestation
Latency from inclusion to birth (days)
Onset of birth
* Spontaneous * Induction * Caesarean section
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Julie Glavind
Lead sponsor
University of Aarhus
Sponsor institution
Aarhus University Hospital
Collaborator
University of Aberdeen
Collaborator
Rigshospitalet, Denmark
Collaborator
Odense University Hospital
Collaborator
Aalborg University Hospital
Collaborator
Zealand University Hospital
Collaborator
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