RecruitingRecruiting
Study Comparing Acceptance and Commitment Therapy to Supportive Diabetes Counseling and a Waitlist Control for Eating Disorders in Type 1 Diabetes
NCT05540704 · Duke University
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
Official title
Changing the T1DE (Type 1 Diabetes Eating Disorders): A Randomized Controlled Trial Comparing Acceptance and Commitment Therapy (ACT) to Supportive Diabetes Counseling and a Waitlist Control
About this study
This is a randomized controlled trial comparing an Acceptance and Commitment Therapy (ACT) protocol to supportive diabetes counseling (SDC) and a Waitlist Control (WLC) for individuals with type 1 diabetes and disordered eating (or T1DE). Both active conditions are tailored to the needs of individuals living with T1D and the unique conditions under which the eating disorder developed and is maintained. Participants will be 161 individuals with T1D, between the ages of 16-50, with binge-purge eating disorders (EDs), including threshold and subthreshold bulimia nervosa, binge eating disorder and purging disorder. Purging includes restriction of insulin for weight loss. An expansion cohort of 74 persons with T1D and elevated Diabetes Eating Problems Survey-Revised scores (DEPS-R=\>20) will also be recruited to assess the utility of the treatments for a broader array of eating and weight control problems in T1D. Participants will be randomized to either ACT, SDC, or a WLC and complete assessments at baseline, mid-treatment, end-of-treatment, and at 1 month, 3 months, and 6 months post-treatment. The primary outcome of interest for power and sample size calculation is blood glucose levels (mean and % time in target glycemic range) as assessed by continuous glucose monitoring. Other outcomes include change in hemoglobin A1c (HbA1c), eating disorder symptoms, diabetes self-management and, secondary, diabetes distress. In addition to examining clinical outcomes, this study tests biobehavioral mechanisms of change and predictors of treatment response. Process of change assessments focus on flexible responding to pathology-relevant stimuli and early improvement in glycemic control affecting executive function. The primary site is Duke University Medical Center. The Miriam Hospital is a secondary site.
Eligibility criteria
Primary Cohort
Inclusion Criteria:
* 16-50 years of age
* Diagnosis of Type 1 diabetes
* Eating disorder characterized by binge eating and/or problematic weight control behaviors, including withholding insulin (Bulimia Nervosa, Binge Eating and Purging Disorder spectrum diagnoses)
* Independently manages diabetes (not reliant on a caregiver)
Expansion Cohort
Inclusion Criteria:
* 16-50 years of age
* Diagnosis of Type 1 diabetes
* DEPR-R score \>=20 but does not meet criteria for the primary cohort
Primary and Expansion Cohort
Exclusion Criteria:
* Active suicidal ideation
* Diagnosis of Avoidant Restrictive Food Intake Disorder or Anorexia Nervosa spectrum diagnoses
* Hypoglycemic unawareness as assessed by the Gold Method and multiple severe episodes of hypoglycemia requiring 3rd party assistance in the last 2 years
* Current substance abuse disorder or current or past psychotic disorder
* NonEnglish speaking
Study design
Enrollment target: 235 participants
Allocation: randomized
Masking: single
Age groups: child, adult
Timeline
Starts: 2023-04-04
Estimated completion: 2027-09
Last updated: 2026-09-08
Interventions
Behavioral: ACTBehavioral: Supportive Diabetes Counseling
Primary outcomes
- • Change in glycemic control as indexed by continuous glucose monitoring (CGM) (baseline, 6 weeks, 12 weeks, 36 weeks)
- • Change in eating disorder symptoms as indexed by the Diabetes Eating Problems Survey-Revised (DEPS-R) (baseline, 12 weeks, 16 weeks, 24 weeks, 36 weeks)
- • Change in diabetes self-management as indexed by the Diabetes Self-Management Questionnaire (baseline, 12 weeks, 16 weeks, 24 weeks, 36 weeks)
Sponsor
Duke University · other
With: The Miriam Hospital, Breakthrough T1D
Contacts & investigators
ContactDottie R Mayo, BA · contact · drm72@duke.edu · (919) 668-1935
ContactRhonda Merwin, PhD · contact · rhonda.merwin@duke.edu · (919) 681-7231
InvestigatorRhonda Merwin, PhD · principal_investigator, Duke University faculty
All locations (2)
Duke UniversityRecruiting
Durham, North Carolina, United States
Brown UniversityRecruiting
Providence, Rhode Island, United States