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Active Implementation phase for Uterine Fibroids (UPFRONT Trial)
N/A
Waitlist Available
Led By Glyn Elwyn, MD, PhD
Research Sponsored by Dartmouth-Hitchcock Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through month 1-6, month 8-14
Awards & highlights
UPFRONT Trial Summary
This study is evaluating whether a patient decision aid can help women make decisions about uterine fibroids.
Eligible Conditions
- Uterine Fibroids
UPFRONT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through month 1-6, month 8-14
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through month 1-6, month 8-14
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
The number of eligible patients that can be identified who receive the uterine fibroid Option Grid patient decision aid.
Secondary outcome measures
Attitudes toward Decision Aids fOr PatienTs (ADOPT)
Chew Health Literacy Measure
Fidelity assessment
+10 moreUPFRONT Trial Design
1Treatment groups
Experimental Treatment
Group I: Active Implementation phaseExperimental Treatment3 Interventions
See the 'detailed description' section to read about the intervention(s) clinicians will use during the active implementation phase of the randomized stepped-wedge design.
Find a Location
Who is running the clinical trial?
Montefiore Medical CenterOTHER
441 Previous Clinical Trials
581,448 Total Patients Enrolled
Brigham and Women's HospitalOTHER
1,609 Previous Clinical Trials
11,469,579 Total Patients Enrolled
Mayo ClinicOTHER
3,206 Previous Clinical Trials
3,766,335 Total Patients Enrolled
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