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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 is a NA study that has completed, run by Rutgers, The State University of New Jersey. The registered enrollment target is 50 participants.

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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.

Interventions

  • BEHAVIORAL Actigraph

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2017-04-01
Est. Completion 2019-08-30
Phase NA

What the Registry Record Tells You About NCT02967016

The ClinicalTrials.gov registry entry for NCT02967016 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rutgers, The State University of New Jersey, which has 413 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Actigraph is the first listed.

NCT02967016 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.