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Multi-component Intervention for Diabetes in Adults With Serious Mental Illness (MIDAS)

Primary Purpose

Schizophrenia, Obesity, Diabetes

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Multi-component Intervention for Diabetes in Adults with Serious Mental Illness
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Schizophrenia focused on measuring Schizophrenia, Serious mental illness, Obesity, Diabetes, Lifestyle Risk Reduction

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Participants: A total of 12 RCFs (30 to 45 beds each), 210 resident participants, and 120 staff members (1 manager, 2 activity directors, 1 cook, and 6 other staff members per facility) will be enrolled.

Inclusion and Exclusion Criteria:

Residential Care Facilities (RCFs):

Inclusion Criteria:

  1. Licensed by California Division of Social Services' Community Care Licensing
  2. Serves only individuals with SMI
  3. Has >15 residents currently living in the facility
  4. Willing to participate

Staff Participants:

Inclusion Criteria:

  1. Age >21 years
  2. Fluent in English
  3. Written informed consent to participate

Exclusion Criteria:

(1) Plans to leave the RCF during the next year.

Resident Participants:

Inclusion Criteria:

  1. Age 18 - 65 years
  2. Chart diagnosis of an SMI, mainly schizophrenia, schizoaffective disorder, or bipolar disorder
  3. Current treatment with antipsychotics
  4. Fluent in English
  5. Written informed consent to participate in this study

Exclusion Criteria:

  1. Chart diagnosis of dementia or intellectual disability disorder
  2. Active substance abuse (non-tobacco)
  3. Medical problems that interfere with ability to complete assessments and intervention

Sites / Locations

  • University of California, San Diego Division of Geriatric PsychiatryRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control Phase

Intervention Phase

Arm Description

3-month initial control phase (no intervention, month 1-3)

6-month intervention phase - MIDAS Intervention Delivered. Followed by 6-month follow-up phase (no intervention, months 10-15).

Outcomes

Primary Outcome Measures

Body Mass Index (BMI in kg/m^2)
Change in Body Mass Index
Waist Circumference
Change in Waist Circumference
Fasting Glucose
Change in Fasting Glucose
Hemoglobin A1c or HbA1c
Change in Hemoglobin A1c or HbA1c

Secondary Outcome Measures

Diet/Nutrition - Plasma Carotenoid Levels
Plasma Carotenoid levels reflect changing dietary vegetable and fruit intake.Nutrition Data Systems for REsearch (NDS-R) Protocol
Diet/Nutrition - Serum Lipid Levels
Plasma Carotenoid levels reflect changing dietary vegetable and fruit intake.
Objective Measure of Physical Activity
For 7 days during each assessment period, participants will wear the GT3X+ Actigraph, which measures movement and intensity of activity, and has good validation with VO2max. It provides estimates of activity by seconds, that can be categorized into minutes spent in sedentary, light, moderate, and vigorous activity using calibration thresholds.
Smoking - Expired Breath Carbon Monoxide (CO) Levels
Change in Smoking - Objective Measure of Cigarette Use: Expired Breath Carbon Monoxide (CO) level (parts per million) is measured with a handheld device. CO monitoring is used primarily as a check on recent smoking, though it has also been used to indicate reductions in smoking.
Smoking - Change in Smoking through Recall
Change in Smoking - Quantity and frequency of cigarette use for the prior week using a timeline followback procedure. Smoking reduction calculated by % change in average cigarettes/day across assessments.

Full Information

First Posted
July 5, 2018
Last Updated
September 15, 2021
Sponsor
University of California, San Diego
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1. Study Identification

Unique Protocol Identification Number
NCT03627377
Brief Title
Multi-component Intervention for Diabetes in Adults With Serious Mental Illness
Acronym
MIDAS
Official Title
Multi-component Intervention for Diabetes in Adults With Serious Mental Illness (MIDAS)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 28, 2018 (Actual)
Primary Completion Date
May 31, 2022 (Anticipated)
Study Completion Date
May 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego

4. Oversight

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

5. Study Description

Brief Summary
Persons with schizophrenia and other serious mental illnesses have a high risk for type 2 diabetes and an increased risk of premature mortality compared to the general population. The goals of the proposed study are to implement a multimodal lifestyle intervention to reduce that risk in these individuals living in residential care facilities, a common housing modality for people with serious mental illnesses. If successful, this intervention will lead to reduction in excess medical comorbidity and mortality in persons with serious mental illnesses.
Detailed Description
Serious mental illnesses (SMI), including schizophrenia, bipolar disorder, and schizoaffective disorder, are associated with increased medical comorbidity and premature mortality from diabetes and cardiovascular disease. Unhealthy lifestyles, including energy-dense (obesogenic) diet, sedentary behavior, and cigarette smoking are important risk factors for diabetes and accelerated biological aging. All of these risk factors are potentially modifiable. There is considerable literature documenting the effectiveness of strategies to prevent and manage diabetes in the general population; yet, these interventions are rarely offered to people with SMI. Residential Care Facilities (RCFs), called Board-and-Care Homes in California, are a common housing modality for patients with SMI; they provide a venue that can maximize efficiency and sustainability of a lifestyle intervention. The goals of the proposed four-year study are to tailor a multi-component intervention to this high-risk group. The study will be a hybrid effectiveness-implementation (Hybrid Type 1) trial of a Multi-component Intervention for Diabetes risk reduction in Adults with SMI (MIDAS) in licensed RCFs in San Diego county. As a Hybrid Type 1 study, the primary emphasis will be on determining the effectiveness of the intervention to achieve desired health outcomes while also systematically collecting data on its implementation within RCFs that will inform implementation strategy refinement. Main components of MIDAS include: (1) Education about diabetes and lifestyle, (2) Dietary intervention at the facility and resident level, (3) Increased physical activity, and (4) Smoking cessation / reduction. The investigators will employ a modified cluster-randomized stepped wedge and adaptive trial design involving 210 residents with SMI and 120 staff members from 12 RCFs. The RCFs will be divided randomly into four cohorts of three RCFs each. Each cohort will be tested over a 15-month period that includes three phases: a three-month initial control phase (no intervention, from baseline month 0 to end of month 3), a six-month intervention phase (months 4 through 9), and a six-month follow-up phase (no intervention, months 10 through 15). All the study participants will be assessed quarterly during the 15-month period. Our investigators will train RCF staff (especially the Activity Director and cook) to increase physical activity and reduce smoking, and to implement healthful dietary modifications among the residents, using evidence-based interventions. During the intervention phase, the RCF Activity Director will conduct twice-weekly manualized group sessions on education about diabetes, nutrition, exercise, and smoking cessation/reduction, to deliver a multi-component group intervention. We will also explore if there are improvements in blood-based research biomarkers of insulin resistance and inflammation in the RCF residents with SMI. This project is responsive to RFA-MH-17-608, and related to NIMH Strategic Objective #3.3B: testing interventions for effectiveness in community practice settings. If successful, MIDAS will be sustained and disseminated, and would lead to reduction in excess medical comorbidity and mortality associated with SMI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Obesity, Diabetes, Lifestyle Risk Reduction, Serious Mental Illness
Keywords
Schizophrenia, Serious mental illness, Obesity, Diabetes, Lifestyle Risk Reduction

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
The investigators will employ a modified cluster-randomized stepped wedge and adaptive trial design involving 210 residents with SMI and 120 staff members from 12 RCFs. The RCFs will be divided randomly into four cohorts of three RCFs each. Each cohort will be tested over a 15-month period that includes three phases: a three-month initial control phase (no intervention, from baseline month 0 to end of month 3), a six-month intervention phase (months 4 through 9), and a six-month follow-up phase (no intervention, months 10 through 15). All the study participants will be assessed quarterly during the 15-month period.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
210 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control Phase
Arm Type
No Intervention
Arm Description
3-month initial control phase (no intervention, month 1-3)
Arm Title
Intervention Phase
Arm Type
Experimental
Arm Description
6-month intervention phase - MIDAS Intervention Delivered. Followed by 6-month follow-up phase (no intervention, months 10-15).
Intervention Type
Behavioral
Intervention Name(s)
Multi-component Intervention for Diabetes in Adults with Serious Mental Illness
Intervention Description
Main components of MIDAS include: (1) Education about diabetes and lifestyle, (2) Dietary intervention at the facility and resident level, (3) Increased physical activity, and (4) Smoking cessation / reduction.
Primary Outcome Measure Information:
Title
Body Mass Index (BMI in kg/m^2)
Description
Change in Body Mass Index
Time Frame
Baseline to 9 months and sustained at 15 months
Title
Waist Circumference
Description
Change in Waist Circumference
Time Frame
Baseline to 9 months and sustained at 15 months
Title
Fasting Glucose
Description
Change in Fasting Glucose
Time Frame
Baseline to 9 months and sustained at 15 months
Title
Hemoglobin A1c or HbA1c
Description
Change in Hemoglobin A1c or HbA1c
Time Frame
Baseline to 9 months and sustained at 15 months
Secondary Outcome Measure Information:
Title
Diet/Nutrition - Plasma Carotenoid Levels
Description
Plasma Carotenoid levels reflect changing dietary vegetable and fruit intake.Nutrition Data Systems for REsearch (NDS-R) Protocol
Time Frame
Baseline to 9 months and sustained at 15 months
Title
Diet/Nutrition - Serum Lipid Levels
Description
Plasma Carotenoid levels reflect changing dietary vegetable and fruit intake.
Time Frame
Baseline to 9 months and sustained at 15 months
Title
Objective Measure of Physical Activity
Description
For 7 days during each assessment period, participants will wear the GT3X+ Actigraph, which measures movement and intensity of activity, and has good validation with VO2max. It provides estimates of activity by seconds, that can be categorized into minutes spent in sedentary, light, moderate, and vigorous activity using calibration thresholds.
Time Frame
Baseline to 9 months and sustained at 15 months
Title
Smoking - Expired Breath Carbon Monoxide (CO) Levels
Description
Change in Smoking - Objective Measure of Cigarette Use: Expired Breath Carbon Monoxide (CO) level (parts per million) is measured with a handheld device. CO monitoring is used primarily as a check on recent smoking, though it has also been used to indicate reductions in smoking.
Time Frame
Baseline to 9 months and sustained at 15 months
Title
Smoking - Change in Smoking through Recall
Description
Change in Smoking - Quantity and frequency of cigarette use for the prior week using a timeline followback procedure. Smoking reduction calculated by % change in average cigarettes/day across assessments.
Time Frame
Baseline to 9 months and sustained at 15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Participants: A total of 12 RCFs (30 to 45 beds each), 210 resident participants, and 120 staff members (1 manager, 2 activity directors, 1 cook, and 6 other staff members per facility) will be enrolled. Inclusion and Exclusion Criteria: Residential Care Facilities (RCFs): Inclusion Criteria: Licensed by California Division of Social Services' Community Care Licensing Serves only individuals with SMI Has >15 residents currently living in the facility Willing to participate Staff Participants: Inclusion Criteria: Age >21 years Fluent in English Written informed consent to participate Exclusion Criteria: (1) Plans to leave the RCF during the next year. Resident Participants: Inclusion Criteria: Age 18 - 65 years Chart diagnosis of an SMI, mainly schizophrenia, schizoaffective disorder, or bipolar disorder Current treatment with antipsychotics Fluent in English Written informed consent to participate in this study Exclusion Criteria: Chart diagnosis of dementia or intellectual disability disorder Active substance abuse (non-tobacco) Medical problems that interfere with ability to complete assessments and intervention
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dilip V Jeste, MD
Phone
(858) 534-4020
Email
djeste@ucsd.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Danielle K Glorioso, LCSW
Phone
(858) 246-0767
Email
dglorioso@ucsd.edu
Facility Information:
Facility Name
University of California, San Diego Division of Geriatric Psychiatry
City
La Jolla
State/Province
California
ZIP/Postal Code
92093
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Danielle K Glorioso, LCSW
Phone
858-246-0767
Email
dglorioso@ucsd.edu
First Name & Middle Initial & Last Name & Degree
Cynthia Ibarra, MA
Phone
(858) 822-6005
Email
cyibarra@ucsd.edu
First Name & Middle Initial & Last Name & Degree
Dilip V Jeste, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Multi-component Intervention for Diabetes in Adults With Serious Mental Illness

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