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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 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).
This trial's timeline: 3 weeks for screening, Varies for treatment, and 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). for reporting.

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 more

Trial 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.

Find a Location

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

Frequently Asked Questions

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~18 spots leftby Apr 2025