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Recruiting NCT04205370

Sleep Behaviors in Pregnancy

No phase Interventional Sleep Pregnancy Complications

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Deactivated Pregnancy Coach, Active Pregnancy Coach.
Who it may be relevant to
Registry conditions: Sleep, Pregnancy Complications. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The researchers would like to know how long pregnant women spend in different positions during the night - and how often women change positions - across pregnancy. The researchers also want to see if the sleep monitor is able to improve sleep behaviors

Interventions

  • Device Deactivated Pregnancy Coach
    Naturalistic monitoring of their typical sleep patterns and behaviors
  • Device Active Pregnancy Coach
    The Pregnancy Coach will begin to deliver alerts when supine sleep is detected. Sleep metrics will be visible on the smartphone app.

Primary outcome measures

  • Proportion of sleep time spent in the supine position as measured by the Pregnancy Coach [Time frame: Until delivery, approximately 12 weeks]
Secondary outcome measures (3)
  • Proportion of sleep time spent with objective snoring as indicated by the Pregnancy Coach [Time frame: Until delivery, approximately 12 weeks]
  • Proportion of participants where their 'going to sleep' position was the same as their dominant sleep position [Time frame: Until delivery, approximately 12 weeks]
  • Percentage of sleep position changes following alert from Pregnancy Coach [Time frame: Until delivery, approximately 12 weeks]

Eligibility criteria

Inclusion criteria

  • At least 28 weeks pregnant
  • Receiving pre-natal care at Michigan Medicine
  • Have either and Android or iPhone smartphone

Exclusion criteria

  • Less then 28 weeks pregnant
  • Receiving pre-natal care external to Michigan Medicine
  • Does not poses a smartphone

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • University of Michigan — Ann Arbor

Identifiers

NCT: NCT04205370 · HUM00140170

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗