← Back to Search

High intensity Interval Training for Pregnancy

N/A
Waitlist Available
Led By Margie H Davenport, PhD
Research Sponsored by University of Alberta
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within one month postpartum
Awards & highlights

Summary

The objective of this randomized cross-over design was to investigate the fetal well-being and maternal glycemic response to an acute bout of aerobic high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) with pregnant individuals.

Eligible Conditions
  • Pregnancy
  • Hypoglycemia
  • Fetal Arrhythmia
  • Fetal Circulation

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within one month postpartum
This trial's timeline: 3 weeks for screening, Varies for treatment, and within one month postpartum for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Fetal Heart Rate
Fetal Umbilical Blood Flow
Flash Glucose Monitor; interstitial Glucose
Secondary outcome measures
Accelerometer
Blood pressure
Cardiac Output
+24 more

Trial Design

2Treatment groups
Experimental Treatment
Group I: 2nd Exercise sessionExperimental Treatment2 Interventions
Participants completed the subsequent exercise protocol (i.e. HIIT or MICT)
Group II: 1st Exercise sessionExperimental Treatment2 Interventions
Participants completed either the HIIT or MICT session.

Find a Location

Who is running the clinical trial?

University of AlbertaLead Sponsor
901 Previous Clinical Trials
387,518 Total Patients Enrolled
Margie H Davenport, PhDPrincipal InvestigatorUniversity of Alberta
~7 spots leftby Jul 2025