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Appropriate Growth for Fetal Growth Restriction
N/A
Recruiting
Research Sponsored by University of Tennessee Graduate School of Medicine
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 pre (within 1 hour of the start of acute exercise bout) to 20 minutes post exercise
Awards & highlights
Study Summary
Objectives / Specific Aims The purpose of this study is to investigate the acute effects of a single bout of moderate intensity maternal exercise on fetal well-being in a pregnancy affected by fetal growth restriction. Fetal well-being will be measured by biophysical profile (BPP), non-stress test (NST) and umbilical artery dopplers. The hypothesis is that a single bout of maternal exercise will not significantly alter fetal well-being or fetal status.
Eligible Conditions
- Fetal Growth Restriction
- Placental Insufficiency
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ pre (within 1 hour of the start of acute exercise bout) to immediately post acute exercise
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre (within 1 hour of the start of acute exercise bout) to immediately post acute exercise
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in umbilical artery dopplers systolic/diastolic ratio from pre to post exercise
Secondary outcome measures
Biophysical Profile (BPP) post exercise
Biophysical Profile (BPP) pre exercise
Change in blood glucose from pre to immediately post acute exercise
+7 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: Fetal Growth RestrictedExperimental Treatment1 Intervention
Pregnant individuals with fetal growth restriction
Group II: Appropriate GrowthExperimental Treatment1 Intervention
Pregnant individuals with normal estimated fetal weight
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Who is running the clinical trial?
University of Tennessee Graduate School of MedicineLead Sponsor
12 Previous Clinical Trials
1,084 Total Patients Enrolled
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