Thrive With Type 1 Diabetes 2026

Part of paid clinical trials in Atlanta, Georgia.

Sponsor
Emory University
Study ID
NCT07522866
Status
Recruiting
Apply to this trial

Conditions

  • Type1diabetes

Eligibility Criteria

Sex
ALL
Age
31 Years - 75 Years
Healthy Volunteers
Accepted

Interventions

  • TranS-C Intervention Arm — BEHAVIORAL
    This 12-week cognitive behavioral intervention uses motivational interviewing and behavior change principles, focusing on self-efficacy and action planning. Participants target 7-9 hours of sleep per night, ≥85% sleep efficiency, and \<60 minutes' variability in bed and wake times. Components include sleep education and hygiene, nightly routines, the management of competing activities, sleep environment optimization, lifestyle modifications (e.g., avoiding caffeine and vigorous exercise before bedtime), screen time reduction, basic stress management (e.g., progressive muscle relaxation), and self-monitoring. Following a baseline visit, a research assistant conducts a 60-minute telehealth session via HIPAA-compliant Zoom/Teams, with booster sessions at weeks 4, 8, and 12. Sleep time is adjusted weekly based on sleep efficiency criteria.
  • Attention Control Enhanced Usual Care (EUC) Arm — BEHAVIORAL
    This time- and attention-balanced 12-week condition will focus on enhancing usual care. After the initial baseline visit, the RA for this group will schedule a 60-minute telehealth appointment for the enhanced usual care. Follow-up sessions (weeks 4 and 8) will focus on health perceptions, care plans, and relationship-building rather than sleep promotion. The RA will encourage participants to share their progress and confidence in their self-set goals to foster engagement and retention. Participants may engage in self-initiated diabetes management, which will be tracked using a Diabetes Self-Management Tracking Form.

Study Details

This study aims to learn whether a cognitive behavioral intervention can improve lifestyle and glucose targets for adults with type 1 diabetes.

Key Dates

Start date
Jul 31, 2026
Status verified
Jun 2026
Primary completion
Apr 30, 2028
Completion
Apr 30, 2028

Study Design

Enrollment
48 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER

Arms

  • Experimental: Transdiagnostic Intervention for Sleep and Circadian (TranS-C) Dysfunction Intervention Arm
    Participants will work with a health coach to aim for 7-9 hours of sleep per night, at least 85% sleep efficiency, and less than 60 minutes' variation in bed and wake times.
  • Active Comparator: Enhanced Usual Care (EUC) Arm
    Participants will work with a health coach focused on enhanced usual care.

Primary Outcome Measure

Multidimensional sleep health composite score [ Time Frame: Baseline and post-intervention (14 weeks from baseline) ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Emory UniversityAtlantaGeorgia30329-
Emory University, Nell Hodgson Woodruff School of NursingAtlantaGeorgia30322-

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By research site
Emory University· Atlanta, GAEmory University, Nell Hodgson Woodruff School of Nursing· Atlanta, GA

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