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

Primary Purpose

Insulin Resistance, Depression, Depressive Disorder

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cognitive-Behavioral Therapy followed by Exercise Training
Exercise Training followed by Cognitive-Behavioral Therapy
Cognitive-Behavioral Therapy Only
Exercise Training Only
Sponsored by
Colorado State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Insulin Resistance focused on measuring Adolescent Type 2 Diabetes Prevention, Exercise Training

Eligibility Criteria

12 Years - 17 Years (Child)FemaleAccepts Healthy Volunteers

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
  • Regular medication use affecting mood, insulin, or weight, including stimulants, anti-depressants, anti-psychotics, insulin sensitizers, weight loss medications & chronic steroids
  • Regular psychotherapy, structured weight loss treatment, or bariatric surgery
  • Pregnancy, nursing

Sites / Locations

  • Children's Hospital ColoradoRecruiting
  • Colorado State UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Active Comparator

Active Comparator

Arm Label

Cognitive-Behavioral Therapy followed by Exercise Training

Exercise Training followed by Cognitive-Behavioral Therapy

Exercise Training Only

Cognitive-Behavioral Therapy Only

Arm Description

6-week cognitive-behavioral therapy intervention of 6 weekly 1-hour group sessions followed by a 6-week exercise training intervention of 6 weekly 1-hour group sessions

6-week exercise training intervention of 6 weekly 1-hour group sessions followed by a 6-week cognitive-behavioral therapy intervention of 6 weekly 1-hour group sessions

6-week exercise training intervention of 6 weekly 1-hour group sessions followed by an additional 6-week exercise training intervention of 6 weekly 1-hour group sessions

6-week cognitive-behavioral therapy intervention of 6 weekly 1-hour group sessions followed by an additional 6-week cognitive-behavioral therapy intervention of 6 weekly 1-hour group sessions

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Insulin sensitivity
Insulin sensitivity index (ISI) derived from fasting and two-hour insulin and glucose as part of oral glucose tolerance testing
Cardiorespiratory fitness
Maximum volume of oxygen (VO2 peak) during cycle ergometry testing using a graded protocol to exertion
Rate Perceived Exertion
Adolescent report on the Borg Scale during cycle ergometry testing
Exercise enjoyment
Adolescent report on the Physical Activity Enjoyment Scale (PACES), total score
Exercise self-efficacy
Adolescent report on the Exercise Self-Confidence Survey, total score
Exercise perceived capability
Adolescent report on the Physical Activity, Patient-Reported outcome Measurement Information System (PROMIS) Short Form
Depression symptoms
Adolescent report on the 20-item Center for Epidemiologic Studies-Depression Scale (CES-D), total score
Depressive disorder
Schedule for Affective Disorders and Schizophrenia for School-Aged Youth - Computerized Version (KSADS-COMP) interview with adolescent
Eating behavior
Habitual macronutrient/food group intake reported 3 days (2 weekdays, 1 weekend) on the Automated Self-Administered 24-Hour Dietary Assessment Tool (ASA24)
Sleep quality
Adolescent report on the Pittsburgh Sleep Quality Index, total score
Sleep disturbance
Adolescent report on the Insomnia Severity Index, total score
BMI
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
Adiposity
Fat/fat-free mass measured via air displacement plethysmography in a fasted state (BodPod)

Full Information

First Posted
August 24, 2022
Last Updated
June 15, 2023
Sponsor
Colorado State University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), University of Colorado, Denver
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1. Study Identification

Unique Protocol Identification Number
NCT05543083
Brief Title
Cognitive-Behavioral Therapy and Exercise Training in Adolescents At-Risk for Type 2 Diabetes
Acronym
CBTeX
Official Title
Cognitive-Behavioral Therapy and Exercise Training in Adolescents At-Risk for Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 2, 2023 (Actual)
Primary Completion Date
January 31, 2027 (Anticipated)
Study Completion Date
April 30, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Colorado State University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), University of Colorado, Denver

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Resistance, Depression, Depressive Disorder, Mood Disorders, Mental Disorder in Adolescence, Hyperinsulinism, Glucose Metabolism Disorders, Metabolic Disease
Keywords
Adolescent Type 2 Diabetes Prevention, Exercise Training

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cognitive-Behavioral Therapy followed by Exercise Training
Arm Type
Experimental
Arm Description
6-week cognitive-behavioral therapy intervention of 6 weekly 1-hour group sessions followed by a 6-week exercise training intervention of 6 weekly 1-hour group sessions
Arm Title
Exercise Training followed by Cognitive-Behavioral Therapy
Arm Type
Active Comparator
Arm Description
6-week exercise training intervention of 6 weekly 1-hour group sessions followed by a 6-week cognitive-behavioral therapy intervention of 6 weekly 1-hour group sessions
Arm Title
Exercise Training Only
Arm Type
Active Comparator
Arm Description
6-week exercise training intervention of 6 weekly 1-hour group sessions followed by an additional 6-week exercise training intervention of 6 weekly 1-hour group sessions
Arm Title
Cognitive-Behavioral Therapy Only
Arm Type
Active Comparator
Arm Description
6-week cognitive-behavioral therapy intervention of 6 weekly 1-hour group sessions followed by an additional 6-week cognitive-behavioral therapy intervention of 6 weekly 1-hour group sessions
Intervention Type
Behavioral
Intervention Name(s)
Cognitive-Behavioral Therapy followed by Exercise Training
Other Intervention Name(s)
CBT->Exercise Training
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Exercise Training followed by Cognitive-Behavioral Therapy
Other Intervention Name(s)
Exercise Training -> CBT
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive-Behavioral Therapy Only
Other Intervention Name(s)
CBT Only
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Exercise Training Only
Intervention Description
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 Outcome Measure Information:
Title
Insulin Resistance
Description
Homeostatic model assessment of insulin resistance (HOMA-IR) estimated from fasting insulin and glucose as part of oral glucose tolerance testing
Time Frame
1-year
Secondary Outcome Measure Information:
Title
Insulin sensitivity
Description
Insulin sensitivity index (ISI) derived from fasting and two-hour insulin and glucose as part of oral glucose tolerance testing
Time Frame
1-year
Title
Cardiorespiratory fitness
Description
Maximum volume of oxygen (VO2 peak) during cycle ergometry testing using a graded protocol to exertion
Time Frame
1-year
Title
Rate Perceived Exertion
Description
Adolescent report on the Borg Scale during cycle ergometry testing
Time Frame
1-year
Title
Exercise enjoyment
Description
Adolescent report on the Physical Activity Enjoyment Scale (PACES), total score
Time Frame
1-year
Title
Exercise self-efficacy
Description
Adolescent report on the Exercise Self-Confidence Survey, total score
Time Frame
1-year
Title
Exercise perceived capability
Description
Adolescent report on the Physical Activity, Patient-Reported outcome Measurement Information System (PROMIS) Short Form
Time Frame
1-year
Title
Depression symptoms
Description
Adolescent report on the 20-item Center for Epidemiologic Studies-Depression Scale (CES-D), total score
Time Frame
1-year
Title
Depressive disorder
Description
Schedule for Affective Disorders and Schizophrenia for School-Aged Youth - Computerized Version (KSADS-COMP) interview with adolescent
Time Frame
1-year
Title
Eating behavior
Description
Habitual macronutrient/food group intake reported 3 days (2 weekdays, 1 weekend) on the Automated Self-Administered 24-Hour Dietary Assessment Tool (ASA24)
Time Frame
1-year
Title
Sleep quality
Description
Adolescent report on the Pittsburgh Sleep Quality Index, total score
Time Frame
1-year
Title
Sleep disturbance
Description
Adolescent report on the Insomnia Severity Index, total score
Time Frame
1-year
Title
BMI
Description
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
Time Frame
1-year
Title
Adiposity
Description
Fat/fat-free mass measured via air displacement plethysmography in a fasted state (BodPod)
Time Frame
1-year
Other Pre-specified Outcome Measures:
Title
Dispositional mindfulness
Description
Adolescent report on the Mindful Attention Awareness Scale - Adolescent Version (MAAS-A), total score
Time Frame
1-year
Title
Weight bias internalization
Description
Adolescent report on the Weight Bias Internalization Scale for Youth (WBIS-Y), total score
Time Frame
1-year
Title
Body image
Description
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.
Time Frame
1-year
Title
Automatic thoughts
Description
Adolescent report of frequency of negative and positive thoughts on the Automatic Thoughts Questionnaire (ATQ), negative and positive scale scores
Time Frame
1-year
Title
Pleasant activities
Description
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
Time Frame
1-year
Title
Intervention Acceptability
Description
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
Time Frame
1-year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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 Regular medication use affecting mood, insulin, or weight, including stimulants, anti-depressants, anti-psychotics, insulin sensitizers, weight loss medications & chronic steroids Regular psychotherapy, structured weight loss treatment, or bariatric surgery Pregnancy, nursing
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lauren B Shomaker, PhD
Phone
970-491-3217
Email
lauren.shomaker@colostate.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Madison Bristol
Phone
720-777-6128
Email
madison.bristol@childrenscolorado.org
Facility Information:
Facility Name
Children's Hospital Colorado
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80011
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Madison Bristol, MPH
Phone
720-777-6607
Email
madison.bristol@childrenscolorado.org
Facility Name
Colorado State University
City
Fort Collins
State/Province
Colorado
ZIP/Postal Code
80523
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Natalia Sanchez, MPH
Phone
970-491-1120
Email
natalia.sanchez@colostate.edu

12. IPD Sharing Statement

Learn more about this trial

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

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