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NCT02967016 · ClinicalTrials.gov registry record · NA
Physical Activity After a Normal Spontaneous or Cesarean Delivery
A NA study, sponsored by Rutgers, The State University of New Jersey.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
NCT02967016: Completed NA study, sponsored by Rutgers, The State University of New Jersey.
NCT02967016 is a NA study that has completed, run by Rutgers, The State University of New Jersey. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02967016, a NA study, has completed, sponsored by Rutgers, The State University of New Jersey.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
Study 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.
Primary Outcome
This will be measured in the numbers of steps registered by the accelerometer
Interventions
- BEHAVIORAL Actigraph
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2017-04-01 |
| Est. Completion | 2019-08-30 |
| Phase | NA |
What the finished NCT02967016 record still lists
NCT02967016 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 1 intervention - of which Actigraph is the first listed.
NCT02967016 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02967016 about?
NCT02967016 is a clinical study titled "Physical Activity After a Normal Spontaneous or Cesarean Delivery". 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 ...
What is the current status of trial NCT02967016?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2017-04-01. Estimated completion is 2019-08-30.
What interventions are being tested in trial NCT02967016?
The interventions under investigation include: Actigraph (BEHAVIORAL).
Who is sponsoring clinical trial NCT02967016?
This trial is sponsored by Rutgers, The State University of New Jersey, which has 413 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02967016's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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