Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
ID05908591

Sleep Disordered Breathing, Endothelial Function, and Adverse Events in Pregnancy Observational Study

Led by University of Alberta · Updated on 2025-05-07

109

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how sleep disordered breathing affects heart and blood vessel health in pregnant individuals. This observational study focuses on whether sleep breathing problems during pregnancy are linked to poorer cardiovascular function and if higher physical activity levels might lower the risk of these breathing problems. The study is led by the University of Alberta to gain insights into maternal health during pregnancy. Participants will complete an 8-day testing protocol at two separate times during pregnancy: first between 20 and 24 weeks gestation, and again between 28 and 36 weeks gestation. During each period, they will undergo one night of at-home sleep testing and overnight vital signs monitoring using devices that track blood pressure and heart rate. They will also wear two accelerometers, maintain a 7-day sleep log, fill out questionnaires, and visit the lab for fasting blood draws and ultrasound assessments measuring cardiovascular health. Throughout the study, participants will be monitored for various heart and blood vessel functions, including endothelial function, arterial stiffness, blood pressure, heart rate, and presence of arrhythmias. Researchers will also assess dietary intake, hormone levels, inflammatory markers, mood, and physical activity. After delivery, a short follow-up survey will collect information on birth outcomes like infant sex, weight, length, gestational age, delivery mode, Apgar score, and time spent in the neonatal intensive care unit. The total participation spans pregnancy through about two months postpartum.

CONDITIONS

Brief Title

Sleep Disordered Breathing, Endothelial Function, and Adverse Events in Pregnancy

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 18 years of age
  • Currently pregnant between 20 and 24 weeks gestation
Not Eligible

You will not qualify if you...

  • Worked shift work past 11pm in the previous month
  • Previously diagnosed with a sleep disorder by a physician
  • Male gender (study limited to females only)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 8 days at each of two time points during pregnancy (20-24 weeks and 28-36 weeks gestation)

Participants complete sleep testing, overnight vital signs monitoring, questionnaires, and wear accelerometers to assess sleep disordered breathing and physical activity during pregnancy.

2 testing periods each including 1 night of at-home sleep testing and overnight vital signs monitoring, wearing accelerometers for 7 days, and completing questionnaires

Monitoring

Duration - At two time points during pregnancy (20-24 weeks and 28-36 weeks gestation)

Participants visit the laboratory for cardiovascular assessments including fasting blood draws and ultrasound tests to evaluate heart and blood vessel health during pregnancy.

2 laboratory visits for fasting blood draw and cardiovascular ultrasound assessments

Long-term Monitoring

Duration - Up to 2 months postpartum

Participants complete a short follow-up survey in the postpartum period to assess maternal and fetal outcomes after delivery.

1 follow-up survey (remote or in-person)

Trial Site Locations

Total: 1 location

1

Program for Pregnancy and Postpartum Health, University of Alberta

Edmonton, Alberta, Canada, T6G 2E1

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Research Team

M

Margie Davenport, PhD

C

Craig Steinback, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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