| NCT ID | NCT04205370 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Michigan |
| Condition | Sleep |
| Study Type | INTERVENTIONAL |
| Enrollment | 500 participants |
| Start Date | 2020-01-22 |
| Primary Completion | 2027-12 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 500 participants in total. It began in 2020-01-22 with a primary completion date of 2027-12.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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
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
Contact & Investigator
Louise O'Brien, PhD
PRINCIPAL INVESTIGATOR
University of Michigan
Frequently Asked Questions
Who can join the NCT04205370 clinical trial?
This trial is open to female participants only, aged 18 Years or older, studying Sleep. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT04205370 currently recruiting?
Yes, NCT04205370 is actively recruiting participants. Contact the research team at louiseo@med.umich.edu for enrollment information.
Where is the NCT04205370 trial being conducted?
This trial is being conducted at Ann Arbor, United States.
Who is sponsoring the NCT04205370 clinical trial?
NCT04205370 is sponsored by University of Michigan. The principal investigator is Louise O'Brien, PhD at University of Michigan. The trial plans to enroll 500 participants.