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CI-PVP (context-informed pre-visit planning) for Type 2 Diabetes
N/A
Waitlist Available
Led By Elizabeth Magnan, MD
Research Sponsored by University of California, Davis
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 change from baseline to 4 months post visit
Awards & highlights
Study Summary
This trialaims to make diabetes care easier for patients by pre-planning visits and reducing workloads for busy clinics.
Eligible Conditions
- Type 2 Diabetes
- Comorbidity
- Multiple Chronic Conditions
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline to 4 months post visit
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline to 4 months post visit
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pilot acceptability)
Pilot feasibility
Secondary outcome measures
Anxiety Symptoms
Blood pressure measurement
Body Mass Index
+11 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
Enhanced PVP
Group II: StandardActive Control1 Intervention
Standard PVP
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Who is running the clinical trial?
University of California, DavisLead Sponsor
910 Previous Clinical Trials
4,706,967 Total Patients Enrolled
Elizabeth Magnan, MDPrincipal InvestigatorUCDavis
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is there still room for participants in this scientific experiment?
"The searchable data hosted on clinicaltrials.gov reveals that this research project is no longer actively seeking candidates; it was initially announced in October of 2020 and last updated in November 2022. Although this particular trial isn't recruiting, there are presently 2334 other studies looking for participants."
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