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Trial record 26 of 66 for:    Behaviors and Mental Disorders[CONDITION-BROWSE-BRANCH] | Recruiting, Not yet recruiting, Available Studies | ( Map: Illinois, United States ) | NIH, U.S. Fed

Engaging Self-regulation Targets to Improve Mood and Weight and Understand Mechanism in Depressed and Obese Adults

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ClinicalTrials.gov Identifier: NCT03841682
Recruitment Status : Recruiting
First Posted : February 15, 2019
Last Update Posted : June 27, 2019
Sponsor:
Collaborators:
Stanford University
University of Washington
National Heart, Lung, and Blood Institute (NHLBI)
Information provided by (Responsible Party):
Jun Ma, University of Illinois at Chicago

Brief Summary:

Multimorbidity (i.e., the coexistence of 2 or more chronic conditions in an individual) is increasingly recognized as a pressing public health problem. Effective interventions targeting coexisting depression and obesity are critical given the high prevalence and worsened outcomes for patients with both conditions.

ENGAGE-2 is a pilot randomized controlled trial (RCT). The objective is to investigate the outcomes and mechanisms of an integrated depression and obesity intervention that combines collaborative stepped depression treatment and evidence-based behavioral weight loss treatment. The Integrated Coaching for Better Mood and Weight-2 (I-CARE2) intervention synergistically integrates 2 proven national programs: the Program to Encourage Active and Rewarding Lives (PEARLS) for depression care and the Group Lifestyle Balance (GLB) program for weight loss and cardiometabolic risk reduction.

In Phase 1 of the ENGAGE project, investigators developed a new protocol to quantify activation and connectivity of the Affective, Cognitive Control, and Default Mode brain circuits from functional magnetic resonance imaging (fMRI) among 108 depressed obese patients. Investigators implement the same fMRI protocol in this second phase of the project to examine the mechanistic role of these brain circuits as potential neural targets in treatment engagement and response in the I-CARE2 intervention. A new sample of 105 depressed obese patients are randomized in a 2:1 ratio to receive the I-CARE2 intervention (n=70) or usual care (n=35). Study assessments occur at 0 (baseline), 2 and 6 months. Investigators hypothesize that 1 or more of the neural targets under study will moderate (baseline state) and/or mediate (change at follow-up) the effect of the I-CARE2 intervention versus usual care on health behaviors (problem-solving ability, dietary intakes, physical activity) and clinical outcomes (weight loss, depression, anxiety).


Condition or disease Intervention/treatment Phase
Obesity Depression Behavioral: I-CARE2 Phase 2 Phase 3

Detailed Description:

Participants in this study are adult patients with comorbid depression and obesity from outpatient clinics in the University of Illinois Hospital and Health Sciences System (UI Health). Participants will be randomly assigned to receive intervention or usual care control.

The I-CARE2 intervention synergistically integrates the PEARLS program for depression care the GLB program for weight loss. The PEARLS program provides problem-solving therapy (PST) as first-line for treating depression, with as-needed antidepressant medication intensification. Adapted from the original Diabetes Prevention Program, the GLB program promotes healthy lifestyle change for weight loss and increased physical activity. For combination treatment, the I-CARE2 intervention provides 9 individual counseling sessions (4 weekly, 2 biweekly, and then 3 monthly; 1 hour each) and participant self-study materials (GLB videos, handouts, weight and activity tracking) over 6 months.

In response to the funding mechanism for this project, the specific aim of the ENGAGE-2 pilot study is to test the degree to which engaging the validated self-regulation target(s) produces desired behavior change important for weight management and mood.


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 105 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Engaging Self-Regulation Targets to Understand the Mechanism of Behavior Change and Improve Mood and Weight Outcomes- Second Phase (ENGAGE-2)
Actual Study Start Date : April 4, 2019
Estimated Primary Completion Date : December 31, 2020
Estimated Study Completion Date : August 31, 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Body Weight

Arm Intervention/treatment
Experimental: I-CARE2 Intervention

Participants should continue with their usual medical care. Additionally, participant receive the I-CARE2 intervention.

Trained health coaches deliver the I-CARE2 intervention over 6 months. The intervention provides 9 individual counseling sessions on problem solving treatment and behavior counselling to manage mood and lose weight (4 weekly, 2 biweekly, and then 3 monthly; 1 hour each), 11 home-viewed GLB videos (weekly; 20-30 minutes each), and self-study and self-monitoring activities. Throughout the intervention, participants are asked to wear and sync a study-provided Fitbit pedometer, and to log their weight, minutes of physical activity, and dietary intake using the Fitbit website or mobile app.

Behavioral: I-CARE2

I-CARE2 intervention synergistically integrates 2 proven national programs: the Program to Encourage Active and Rewarding Lives (PEARLS) for depression care and the Group Lifestyle Balance (GLB) program for weight loss and cardiometabolic risk reduction.

The PEARLS program provides problem-solving therapy (PST) as first-line for treating depression, with as-needed antidepressant medication intensification. Adapted from the original Diabetes Prevention Program, the GLB program promotes healthy lifestyle change for weight loss and increased physical activity.


No Intervention: Usual Care
Participants should continue with their Usual Medical Care. Additionally, participants receive information on wellness and behavioral health promotion at UI Health and a Fitbit pedometer.



Primary Outcome Measures :
  1. Change in Boby Mass Index (BMI) at 6 months [ Time Frame: Baseline, 6 months ]
    BMI will be calculated based on height and weight measured per standard protocols

  2. Change in Depression Symptom Checklist 20 items (SCL-20) at 6 months [ Time Frame: Baseline, 6 months ]
    The SCL-20 is a valid, reliable measure of depression severity, scores ranging from 0 (best) to 4 (worst). SCL-20 cutoff points of 1.5 and 2.0 correspond to moderate and severe depression, respectively. It has been used in numerous depression treatment trials in primary care and community settings, making it particularly useful for cross-study comparisons and data synthesis in meta-analyses.


Secondary Outcome Measures :
  1. Dietary Intake [ Time Frame: Baseline, 2 months, 6 months ]
    Dietary intake will be recorded using 24-hours dietary recalls

  2. Fruit, vegetable, fat and fiber intake [ Time Frame: Baseline, 2 months, 6 months ]
    17-item fruit, vegetable, fat, and fiber screener will be used.

  3. Physical activity (PA) [ Time Frame: Baseline, 2 months, 6 months ]
    PA will be measured using 7-day Physical Activity Recall

  4. Steps [ Time Frame: Baseline, 2 months, 6 months ]
    Steps will be calculated using Fitbit

  5. Problem solving [ Time Frame: Baseline, 2 months, 6 months ]
    Problem Solving will be evaluated using Social Problem-Solving Inventory-Revised: Short Form

  6. Self-regulation of emotion, cognition, and self-reflection [ Time Frame: Baseline, 2 months, 6 months ]
    fMRI scan will be used to evaluate self-regulation of emotion, cognition, and self-reflection

  7. Weight (kg) [ Time Frame: Baseline, 2 months, 6 months ]
    Measured using a weight scale. Missing study-measured weight may be replaced with weight from electronic health records or self-reported weight.

  8. Clinically significant weight change from baseline [ Time Frame: 2 months, 6 months ]
    Dichotomous variable based on if participants reaching 5% weight loss from baseline.

  9. Self-regulation of emotion, cognition, & self-reflection [ Time Frame: Baseline, 2 months, 6 months ]
    BiAffect (Smart phone passive data collection) will be used, as an alternative, to evaluate self-regulation of emotion, cognition, and self-reflection

  10. Depression Response [ Time Frame: 2 months, 6 months ]
    This will be evaluated using depression symptom checklist SCL-20 (50% decline in SCL-20 scores from baseline)

  11. Complete Depression Remission [ Time Frame: 2 monts, 6 months ]
    Evaluated using depression symptom checklist SCL-20 (SCL-20 <0.5)

  12. Change in Body Mass Index (BMI) at 2 months [ Time Frame: Baseline, 2 months ]
    BMI will be calculated based on height and weight measured per standard protocols

  13. Change in Depression Symptom Checklist 20 items (SCL-20) at 2 months [ Time Frame: Baseline, 2 months ]
    The SCL-20 is a valid, reliable measure of depression severity, scores ranging from 0 (best) to 4 (worst). SCL-20 cutoff points of 1.5 and 2.0 correspond to moderate and severe depression, respectively. It has been used in numerous depression treatment trials in primary care and community settings, making it particularly useful for cross-study comparisons and data synthesis in meta-analyses.

  14. Blood pressure [ Time Frame: Baseline, 2 months, 6 months ]
    The American Heart Association recommendations for BP measurement will be followed. BP will be measured in the seated position after at least a 5-minute rest in a separate, quiet room where no other activity is taking place and where temperature fluctuations are minimal. At baseline, both arms will be measured once and 2 more times on the arm with higher systolic reading using standard equipment. This same arm will be measured 3 times at each follow-up assessment. Wait 1 minute between each measurement.

  15. Waist circumference [ Time Frame: Baseline, 2 months, 6 months ]
    Waist circumference will be measured using a study-provided body tape measure placed on bare skin in a horizontal plane around the abdomen at the uppermost lateral border of the right iliac crest. Waist circumference will be measured to the nearest 0.1 centimeters. Two measurements will be taken, and if the measurements differ by 1.0 cm or more, then take a third.

  16. Sleep and wake function [ Time Frame: Baseline, 2 months, 6 months ]
    Sleep quality will be assessed on the 8-item PROMIS sleep disturbance (SD) and sleep-related impairment (SRI) scales short forms. The former measures symptoms of insomnia and the latter measures symptoms of daytime sleepiness. Each item is scaled from 1 (not at all) to 5 (very much). Correlation between the SD short form and the Pittsburgh Sleep Quality Index (PSQI, hypothesized to measure similar attributes) is 0.83 and correlation between the SRI short form and the Epworth Sleepiness Scale (ESS, hypothesized to measure a related but slightly different construct, the propensity to doze during activities) is 0.46, similar to the correlations between the SD full banks and PSQI (0.85) and between SRI full banks and the ESS (0.45).

  17. Anxiety [ Time Frame: Baseline, 2 months, 6 months ]
    Anxiety is measured using Generalized Anxiety Disorder Scale (GAD-7).

  18. Anxiety [ Time Frame: Baseline, 6 months ]
    Anxiety is measured using Panic Disorder module of the Mini-International Neuropsychiatric Interview (MINI).

  19. Perceived stress [ Time Frame: Baseline, 6 months ]
    Perceived stress is measured using Perceived stress scale (PSS). PSS measures the perception of stress (i.e., the degree to which situations in one's life are appraised as stressful). PSS contains 14 items, rated on a 5-point scale ranging from "never" to "very often." After reversing the scores on 7 positive items, a sum of score is calculated with higher score indicating higher perceived stress. Cronbach's alpha ranged from 0.84 to 0.86.

  20. Disability [ Time Frame: Baseline, 6 months ]
    Disability is measured using Sheehan Disability Scale. The Sheehan Disability Scale is a validated questionnaire that measures functional disability and is sensitive to treatment effects in clinical trials. Patients rate the extent to which their symptoms impair work/school, social, and family life on a visual analog scale from0 to 10 and answer the number of days when their symptoms cause them to miss work/school and be unproductive at work/school.

  21. Generic health related quality of life [ Time Frame: Baseline, 6 months ]
    Generic health related quality of life is measured using SF-8 Health Survey. The SF-8 is an 8-item version of the SF-36 that measures overall health-related quality of life. Physical and mental health composite scores are computed using the scores of 8 questions and range from 0 to 100, with 0 indicating the lowest level of health and 100 indicating the highest level of health. Correlation between the SF-8 and the SF-36 is 0.825 for physical health component and 0.881 for mental health component.

  22. Obesity-specific health related questions [ Time Frame: Baseline, 6 months ]
    The Obesity-Related Problem Scale specifically measures the impact of obesity on psychosocial functioning. The 8-item scale has high internal reliability and sound test-retest reliability, correlates strongly with a wide range of theoretically related constructs, and is responsive to weight loss intervention.

  23. Posttraumatic stress disorder [ Time Frame: Baseline, 6 months ]
    Posttraumatic stress disorder is measured using the 17-item PTSD checklist - Civilian Version (PCL-C) that has high reliability and validity.

  24. Pain [ Time Frame: Baseline, 6 months ]
    Pain is measured using PROMIS SF - Pain Interference 4a and Numeric Rating Scale - Pain Intensity 1a.

  25. Binge eating severity [ Time Frame: Baseline, 6 months ]
    Binge eating severity is measured using the Binge eating severity scale.

  26. Medication adherence [ Time Frame: Baseline, 2 months, 6 months ]
    Medication adherence is measured using the 8-Item Morisky Medication Adherence Scale (MMAS-8).



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Age: ≥18 years
  • Body mass index based on study measurements at baseline group orientation: ≥30.0 kg/m2 (≥27.0 if Asian), and weight <350 pounds (due to fMRI scanner size limitations)
  • Elevated depressive symptoms as per 9-item Patient Health Questionnaire (PHQ-9) scores ≥10 on study screening
  • UI Health patient seen in primary care at least once in the preceding 18 months
  • Able and willing to enroll and provide written informed consent

Exclusion Criteria:

  • Active suicidal ideation based on PHQ-9 or the 20-item depression symptom checklist (SCL-20) that includes active plan and/or intent
  • Any other psychiatric disorder other than persistent depressive disorder and/or major depressive disorder, with the exception of any comorbid anxiety disorder
  • Active Bulimia Nervosa within the past 3 months (however Binge Eating Disorder without purging is not an exclusionary condition)
  • Active alcohol or substance use disorder (including prescription drugs)
  • Currently under the care of a psychiatrist or licensed mental health therapist outside of UI Health
  • Had bariatric surgery (e.g., bypass, banding, sleeve, or biliopancreatic diversion with duodenal switch) within the past 12 months or plan to undergo bariatric surgery during the study period
  • Pre-existing diabetes (other than during pregnancy)
  • Pre-existing cardiovascular disease: e.g., coronary heart disease (myocardial infarction, angina pectoris, percutaneous coronary intervention, and coronary artery bypass graft surgery), cerebrovascular disease (stroke, transient ischemic attack), peripheral vascular disease, heart failure, or aortic aneurysm.
  • Diagnosis of cancer (other than non-melanoma skin cancer) that is/was active or treated with radiation or chemotherapy within the past year
  • Severe medical comorbidities that require aggressive treatment, e.g., stage 4 or greater renal disease, and liver failure
  • Diagnosis of a terminal illness and/or residence in a long-term care facility
  • Cognitive impairment based on the Callahan 6-item screener
  • MRI is contraindicated (weight over 350 pounds, traumatic brain injury, tumor or any other known structural abnormality in brain, bullet, shrapnel, or other projectile above the shoulder, not being able to lie down in an fMRI scanner for about an hour due to claustrophobia, personal history of epilepsy, convulsions, or seizures, have piercings that cannot be removed)
  • Traumatic brain injury; Tumor or any other known structural abnormality in brain
  • Inability to speak, read or understand English
  • No reliable telephone service, or no regular Internet access via a computer and/or mobile device (e.g., smartphone)
  • Plan to move out of the area or transfer care outside UI Health during the study period
  • Currently pregnant, lactating, or planning to become pregnant during the study period
  • Already enrolled, or planning to enroll, in another medical or behavioral intervention research study
  • Family/household member of another participant or of a staff member
  • Investigator discretion for clinical safety or protocol adherence reasons

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03841682


Contacts
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Contact: Jun Ma, MD, PhD 312-413-9830 maj2015@uic.edu
Contact: Justine Kessler, MPH 312-413-9831 jkessl4@uic.edu

Locations
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United States, Illinois
Institute for Health Research and Policy (IHRP), Center for Health Behavior Research Recruiting
Chicago, Illinois, United States, 60608
Contact: Jun Ma, MD, PhD         
UIMC Advanced Imaging Center Recruiting
Chicago, Illinois, United States, 60612
Contact: Jun Ma         
Sponsors and Collaborators
University of Illinois at Chicago
Stanford University
University of Washington
National Heart, Lung, and Blood Institute (NHLBI)
Investigators
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Principal Investigator: Jun Ma, MD,PhD University of Illinois at Chicago

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Responsible Party: Jun Ma, Professor of Medicine, Director of Center for Health Behavior Research, MD, PhD, FAHA, FABMR, University of Illinois at Chicago
ClinicalTrials.gov Identifier: NCT03841682     History of Changes
Other Study ID Numbers: 2018-1174
UH3HL132368 ( U.S. NIH Grant/Contract )
First Posted: February 15, 2019    Key Record Dates
Last Update Posted: June 27, 2019
Last Verified: June 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No