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NCT Number: NCT05543083

Cognitive-Behavioral Therapy and Exercise Training in Adolescents At-Risk for Type 2 Diabetes

The investigators are doing this study to learn more about how to prevent type 2 diabetes in teenage girls. The purpose of this study is to find out if taking part in a cognitive-behavioral therapy group, exercise training group, or a combination of cognitive-behavioral therapy and exercise training groups, decreases stress, improves mood, increases physical activity and physical fitness, and decreases insulin resistance among teenagers at risk for diabetes.

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Key information

Age range

12 year–17 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Children's Hospital Colorado, Aurora, Colorado, United States

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About this study

There has been rapid escalation in adolescent-onset type 2 diabetes (T2D), particularly in females from historically disadvantaged racial/ethnic groups. Prevention is critical because adolescent-onset T2D often shows a more aggressive disease course than adult-onset, and effective treatment options remain elusive. Standard-of-care for T2D prevention includes exercise training to ameliorate insulin resistance, a key physiological precursor to T2D. Despite short-term benefits, exercise training shows insufficient effectiveness in adolescents at-risk for T2D. Depression may be explanatory in a considerable subset of teenagers. Adolescence is notable for increases in depression and decreases in physical activity, especially in females with obesity. Youths' depression symptoms contribute to worsening insulin resistance over time, independent of BMI (kg/m2), likely through stress-mediated pathways such as reduced physical activity and fitness. Also, adolescent depression is associated with decreased physical activity and cardiorespiratory fitness, even after accounting for adiposity, and depression predicts greater non-adherence to exercise training. The central theme of this proposal is that an intervention sequence of delivering cognitive-behavioral therapy (CBT) first, followed by intervening with exercise training second, will offer a targeted, efficacious strategy for improving insulin resistance and consequently, lowering T2D risk in adolescent females at-risk for T2D with depression symptoms. In a prior National Institute of Health (NIH) /National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) K99/R00 randomized controlled trial (RCT), the investigators found that 6-week group CBT decreased depression at 6-week follow-up in adolescent females at-risk for T2D with moderately elevated depression, compared to a 6-week didactic health education control group. Adolescents with elevated depression who were randomized to CBT had lower fasting and 2-hour insulin at 1-year vs. controls. Our preliminary data suggest that CBT's focus on enhancing frequency/enjoyment of physical activity to combat depressed mood partially explained why decreasing depression lowered T2D risk. It is not known if CBT is just as efficacious as standard-of-care exercise training, or whether CBT followed by exercise training results in a maximally potent alleviation of T2D risk in adolescent females at-risk for T2D with depression symptoms. To address these gaps and directly build on our prior work, the investigators propose a four-arm RCT to: (1) Compare the efficacy of four 6-week-->6-week sequences for improving insulin resistance in N=300 adolescent females at-risk for T2D with elevated depression symptoms: (i) CBT-->exercise, (ii) exercise-->CBT, (iii) CBT only (CBT-->continue CBT), and (iv) exercise only (exercise-->continue exercise); (2) Evaluate physical activity/fitness as mediators underlying the depression-insulin resistance association; and (3) Evaluate underlying mechanisms by which decreasing depression increases physical activity and improves fitness and insulin resistance using a mixed-methods process evaluation. Findings will support our long-term goal to identify feasible, cost-effective intervention strategies with high potential for effective dissemination to adolescents at-risk for T2D with elevated depression symptoms.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female
  • Age 12-17 years
  • Body Mass Index (BMI)>= 85 for age and sex
  • Type 2 Diabetes (T2D) first-or second-degree relative
  • Center for Epidemiologic Studies Depression Scale (CES-D) total score >=21

Exclusion criteria

  • T2D/ Type 1 Diabetes (T1D) or any major medical condition (e.g. cardiovascular, renal) that would prohibit the ability to participate in exercise training
  • Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) conduct disorder, substance abuse/ dependence, obsessive compulsive disorder, panic attacks, post-traumatic stress disorder, anorexia/bulimia, & schizophrenia
  • Insulin sensitizers, weight loss medications & chronic steroids
  • Structured weight loss treatment or bariatric surgery
  • Pregnancy, nursing

Treatment and study plan

Cognitive-Behavioral Therapy followed by Exercise Training

Behavioral

6-week group CBT (cognitive-behavioral therapy; 1 hour/week for 6 weeks) followed by 6-week group exercise training (1 hour/week for 6 weeks). Home practice is assigned throughout the 12-week intervention period.

Other names: CBT->Exercise Training

Exercise Training followed by Cognitive-Behavioral Therapy

Behavioral

6-week group exercise training (1 hour/week for 6 weeks) followed by 6-week group CBT (1 hour/week for 6 weeks). Home practice is assigned throughout the 12-week intervention period.

Other names: Exercise Training -> CBT

Cognitive-Behavioral Therapy Only

Behavioral

6-week group CBT (1 hour/week for 6 weeks), with continuation of group CBT for a second 6-week period (1 hour/week for 6 weeks). Home practice is assigned throughout the 12-week intervention period.

Other names: CBT Only

Exercise Training Only

Behavioral

6-week group exercise training (1 hour/week for 6 weeks), with continuation of group exercise for a second 6-week period (1 hour/week for 6 weeks). Home practice is assigned throughout the 12-week intervention period.

Primary outcomes

  1. Insulin Resistance

    Time frame: 1-year

    Homeostatic model assessment of insulin resistance (HOMA-IR) estimated from fasting insulin and glucose as part of oral glucose tolerance testing

Secondary outcomes

  1. Insulin sensitivity

    Time frame: 1-year

    Insulin sensitivity index (ISI) derived from fasting and two-hour insulin and glucose as part of oral glucose tolerance testing

  2. Cardiorespiratory fitness

    Time frame: 1-year

    Maximum volume of oxygen (VO2 peak) during cycle ergometry testing using a graded protocol to exertion

  3. Rate Perceived Exertion

    Time frame: 1-year

    Adolescent report on the Borg Scale during cycle ergometry testing

  4. Exercise enjoyment

    Time frame: 1-year

    Adolescent report on the Physical Activity Enjoyment Scale (PACES), total score

  5. Exercise self-efficacy

    Time frame: 1-year

    Adolescent report on the Exercise Self-Confidence Survey, total score

  6. Exercise perceived capability

    Time frame: 1-year

    Adolescent report on the Physical Activity, Patient-Reported outcome Measurement Information System (PROMIS) Short Form

  7. Depression symptoms

    Time frame: 1-year

    Adolescent report on the 20-item Center for Epidemiologic Studies-Depression Scale (CES-D), total score

  8. Depressive disorder

    Time frame: 1-year

    Schedule for Affective Disorders and Schizophrenia for School-Aged Youth - Computerized Version (KSADS-COMP) interview with adolescent

  9. Eating behavior

    Time frame: 1-year

    Habitual macronutrient/food group intake reported 3 days (2 weekdays, 1 weekend) on the Automated Self-Administered 24-Hour Dietary Assessment Tool (ASA24)

  10. Sleep quality

    Time frame: 1-year

    Adolescent report on the Pittsburgh Sleep Quality Index, total score

  11. Sleep disturbance

    Time frame: 1-year

    Adolescent report on the Insomnia Severity Index, total score

  12. BMI

    Time frame: 1-year

    Derived from height in triplicate by stadiometer and fasting weight by calibrated scale; raw (kg/m2) and z-score/percentile based upon Centers for Disease Control and Prevention (CDC) growth charts

  13. Adiposity

    Time frame: 1-year

    Fat/fat-free mass measured via air displacement plethysmography in a fasted state (BodPod)

Other outcomes

  1. Dispositional mindfulness

    Time frame: 1-year

    Adolescent report on the Mindful Attention Awareness Scale - Adolescent Version (MAAS-A), total score

  2. Weight bias internalization

    Time frame: 1-year

    Adolescent report on the Weight Bias Internalization Scale for Youth (WBIS-Y), total score

  3. Body image

    Time frame: 1-year

    Multidimensional Body Self-Relations Questionnaire Measure composed of 10 subscales: appearance evaluation, fitness evaluation, fitness orientation, health evaluation, health orientation, illness orientation, body areas satisfaction, overweight preoccupation, and self-classified weight.

  4. Automatic thoughts

    Time frame: 1-year

    Adolescent report of frequency of negative and positive thoughts on the Automatic Thoughts Questionnaire (ATQ), negative and positive scale scores

  5. Pleasant activities

    Time frame: 1-year

    Adolescent report on the frequency and perceived pleasantness of physical and social activities on the Pleasant Events Schedule (PES), frequency and pleasantness scales for physical activities and for social activities

  6. Intervention Acceptability

    Time frame: 1-year

    Equal or greater than 80% adolescent liking/credibility ratings (equal or greater than 4 on a scale of 1=not at all to 5=extremely) on a Program Acceptability Questionnaire and themes indicative of liking/perceived benefit on standardized interviews for qualitative coding

Study contacts

Contact information is provided by the study sponsor or research team.

Lauren B Shomaker, PhD

CONTACT

[email protected]

970-491-3217

Madison Bristol

CONTACT

[email protected]

720-777-6128

Sponsors and collaborators

Lead sponsor

Colorado State University

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  • University of Colorado, Denver

Registry information

Acronym: CBTeX

Important dates

Study start
2023
Primary completion
2028
Study completion
2029
First posted
Sep 16, 2022
Registry last updated
Apr 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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