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Behavioral Intervention
Counterfactual Intervention for Type 2 Diabetes
N/A
Waitlist Available
Research Sponsored by Texas A&M University
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 collected via survey measures at baseline (study visit #1), 4 weeks (study visit #3), at 6 weeks (study visit #4), 14 weeks (study visit #5), and 22 weeks (study visit #6).
Awards & highlights
Study Summary
This trial will test whether food-based photo diaries and continuous glucose monitors can help people with prediabetes make better food choices.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ collected via survey measures at baseline (study visit #1), 4 weeks (study visit #3), at 6 weeks (study visit #4), 14 weeks (study visit #5), and 22 weeks (study visit #6).
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~collected via survey measures at baseline (study visit #1), 4 weeks (study visit #3), at 6 weeks (study visit #4), 14 weeks (study visit #5), and 22 weeks (study visit #6).
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in HbA1C
Change in average daily glucose level
Change in number of glucose excursions and time in range
Secondary outcome measures
Change in General Health Intentions (GHI) scores
Change in Regulation of Eating Behaviors Scale (REBS) scores
Change in the Behavioral Strategies - Engagement and Intentions score
+2 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention GroupExperimental Treatment1 Intervention
Participants in this group will complete the same measures as the control group, but will additionally be involved in a counterfactual intervention conducted by an advanced graduate student.
Group II: Control GroupActive Control1 Intervention
Participants in this group will complete the same measures as the experimental group. Instead of being involved in a counterfactual intervention, participants will be asked about their intentions to complete future study components.
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Who is running the clinical trial?
Texas A&M UniversityLead Sponsor
139 Previous Clinical Trials
23,865 Total Patients Enrolled
U.S. National Science FoundationFED
34 Previous Clinical Trials
8,824 Total Patients Enrolled
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