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N/A N=50 Prevention

Physical Activity After a Normal Spontaneous or Cesarean Delivery

Postpartum Disorder

Enrolled (actual)
50
Serious AEs
0.0%
Results posted
Jun 2020
Primary outcome: Primary: Steps — 968; 1771; 1652; 3165 Steps — p=0.002

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Actigraph (Behavioral)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
Rutgers, The State University of New Jersey
Primary completion
Jul 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Steps
968; 1771; 1652; 3165; 3421; 5911 0.002 sig
SECONDARY
Pain Score at Rest
25; 14; 27; 22; 28; 13 0.06
SECONDARY
Satisfaction Scores
71; 78; 69; 80; 60; 83 .43

Summary

To the best of the investigators knowledge the average level of physical activity (PA) of parturients recovering from a cesarean delivery or after a normal spontaneous vaginal delivery (NSVD) remains unknown. Taking in consideration that parturients are in a hypercoagulable state and that obstetric venous thromboembolism (VT) is one of the most common causes of maternal morbidity and mortality, ambulation is of utmost importance to anesthesiologists as well as obstetricians. In order to promote mobility, first the investigators need to learn the average parturients level of physical activity in the immediate post-partum period and up to 48 hours after delivery. This information may help us promote mobility in the immediate postpartum period, particularly for those that underwent a cesarean delivery since they are at higher risk of VT.

Eligibility Criteria

Inclusion Criteria

  • Women 18-45 years old giving birth after receiving a neuraxial analgesia/anesthesia technique. American Society of Anesthesiologists classification 1-2.

Exclusion Criteria

  • History of chronic pain
  • Recent use of opioids (other than postpartum)
  • Emergency case requiring general anesthesia (GA) or conversion to GA
  • BMI > 45
  • Need to perform more extensive surgery (i.e Hysterectomy) Need for the neonate to be admitted to NICU (This will prompt mothers to walk more frequently, and longer distances to visit the baby)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02967016). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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