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Diabetes-Depression Care-management Adoption Trial (DCAT)

Primary Purpose

Depression, Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Technology-supported care
Sponsored by
University of Southern California
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Depression focused on measuring Depression screening, Depression monitoring, Chronic illness, Behavioral health, Care management, Automatic telephone assessment, Clinical decision support, Suicide alert

Eligibility Criteria

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

Inclusion Criteria:

  • age equal to or greater than 18 years
  • receiving primary care at DHS safety net clinics
  • having a current diagnosis of type 2 diabetes mellitus (non-gestational).
  • have a working telephone or cellular phone.

Exclusion Criteria:

  • current suicidal ideation;
  • inability to speak either English or Spanish;
  • a score of 2 or greater on the CAGE (4M) alcohol assessment;
  • having schizophrenia, schizoaffective disorder, manic-depressive, or needing lithium;
  • and cognitive impairment precluding ability to give informed consent or participating in the intervention, i.e., Short Portable Mental Status Questionnaire(SPMSQ) score of 6 or more errors.

Provider and administrator inclusion criteria are: practicing or managing at one of the eight study sites; involved with diabetes or depression care

No specific exclusion criteria will be applied to providers and administrators.

Sites / Locations

  • El Monte Comprehensive Health Center
  • High Desert Comprehensive Health Center
  • Long Beach Comprehensive Health Center
  • H. Claude Hudson Comprehensive Health Center
  • Roybal Comprehensive Health Center
  • Olive View-UCLA Medical Center Diabetes Clinic
  • Mid-Valley Comprehensive Health Center
  • Harbor Comprehensive Health Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

No Intervention

No Intervention

Arm Label

Technology-supported care

Supported-Care

Usual Care

Arm Description

This arm consists of Clinic Resource Management (CRM) clinics and serves as our intervention arm where the tested technology is implemented. Our overarching aim in these comparisons is to assess the potential effects of technology-facilitated depression symptom monitoring, relapse prevention, and medication adjustments and to examine depression care receipt and symptom improvement, patient/provider acceptance, and cost.

This arm consists of CRM (Clinic Resource Management) clinics and serves as one of the two control arms in the study.

This arm consists of non-CRM (Clinic Resource Management) clinics and serves as one of the two control arms in the study.

Outcomes

Primary Outcome Measures

Change from baseline in depression outcome at 6-months
Depression is measured using depression scales Patient Health Questionnaire (PHQ)-9. Major depression is classified as PHQ-9>=10.

Secondary Outcome Measures

Change from baseline in diabetes self-care score in 6 months
Diabetes self-care is measured using the Toolbert diabetes self-care scale.

Full Information

First Posted
January 29, 2013
Last Updated
December 3, 2014
Sponsor
University of Southern California
Collaborators
Department of Health and Human Services
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1. Study Identification

Unique Protocol Identification Number
NCT01781013
Brief Title
Diabetes-Depression Care-management Adoption Trial
Acronym
DCAT
Official Title
Care Management Technology to Facilitate Depression Care in Safety Net Diabetes Clinics
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern California
Collaborators
Department of Health and Human Services

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The specific aims of the proposed study are to: Develop the innovative depression care management technology, including the speech recognition technology for automated monitoring and patient prompts over time, automatic integration of the responses into the patient registry, and evidence-based decision-support algorithms for care actions; Conduct the quasi-experiment in eight Los Angeles County Department of Health Services (LAC-DHS) clinics to test the interventions; Use mixed-method evaluation to assess the extent of the implementation of the interventions, the acceptance to the providers and to the patients, and the impact on adoption of depression screening and treatment management over time, utilization, and cost of healthcare services, and patient health outcomes; and Conduct a cost-effectiveness analysis of the three study arms. Successful completion of the study will demonstrate which Comparative Effectiveness Research (CER) adoption strategies are successful and why, their comparative cost-effectiveness, as well as which strategies are successful under which circumstances to inform system-wide implementation of same. Hypotheses of the Proposed Study The following are the main hypotheses of the study: There will be statistically significant difference in the adoption of depression care screening and management over time among the three study groups. 1.1. The adoption rate will be Technology-supported care (TC) > Supported Care (SC) > Usual Care (UC). There will be statistically significant difference in the depression symptom reduction, and better functional status, and quality of life among the three study groups. 2.1. The difference between the TC and the SC will not be statistically significant, but both will be greater than the UC group. There will be statistically significant difference in the diabetes care process and outcomes among the three study groups. 3.1. The difference between the TC and the SC will not be statistically significant, but both will be greater than the UC group. There will also be statistically significant differences in healthcare utilization among the three study groups, with least utilization in the TC group where the greatest level of technology is applied. Of the three groups compared, the TC group will be the most cost-effective approach for accelerating adoption of the CER depression care results.
Detailed Description
In addition, the study will aim to answer the secondary research questions listed below: What is medical provider satisfaction with the technology used in the TC (Technology Care) group? What is patient acceptance with the technology used in the TC group? What factors are identified by medical providers and clinic administrators as related to satisfaction, barriers, and sustaining the intervention post-trial? What are patients' reported satisfaction and facilitating factors and barriers to receipt and acceptance of depression care?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Diabetes Mellitus
Keywords
Depression screening, Depression monitoring, Chronic illness, Behavioral health, Care management, Automatic telephone assessment, Clinical decision support, Suicide alert

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1485 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Technology-supported care
Arm Type
Experimental
Arm Description
This arm consists of Clinic Resource Management (CRM) clinics and serves as our intervention arm where the tested technology is implemented. Our overarching aim in these comparisons is to assess the potential effects of technology-facilitated depression symptom monitoring, relapse prevention, and medication adjustments and to examine depression care receipt and symptom improvement, patient/provider acceptance, and cost.
Arm Title
Supported-Care
Arm Type
No Intervention
Arm Description
This arm consists of CRM (Clinic Resource Management) clinics and serves as one of the two control arms in the study.
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
This arm consists of non-CRM (Clinic Resource Management) clinics and serves as one of the two control arms in the study.
Intervention Type
Other
Intervention Name(s)
Technology-supported care
Intervention Description
The depression care-management technology that will interact with patients is the Automated Speech Recognition (ASR) for remote monitoring data collection. The ASR will use automated telephone calls to reach out to patients to repeat depression screening using PHQ-9, triggered either by calendar date or upcoming appointments, and to remind patients of their appointments in pre-determined time. In addition, the ASR will apply a structured script to conduct automatic follow-up with patients regarding their depression treatment adherence and side effects in order to provide data to help primary medical providers promptly and optimally adapt treatment. The ASR script will also include structured relapse prevention prompts. For providers and administrators, the depression care-management technology aimed to improve their workflow regarding depression care is Enhanced Disease Registry (EDR)..
Primary Outcome Measure Information:
Title
Change from baseline in depression outcome at 6-months
Description
Depression is measured using depression scales Patient Health Questionnaire (PHQ)-9. Major depression is classified as PHQ-9>=10.
Time Frame
6-months from enrollment
Secondary Outcome Measure Information:
Title
Change from baseline in diabetes self-care score in 6 months
Description
Diabetes self-care is measured using the Toolbert diabetes self-care scale.
Time Frame
6 months from enrollment
Other Pre-specified Outcome Measures:
Title
Change from baseline in physical functional status in 6 months
Description
Physical functional status is measured using the physical component score of the SF-12 scale
Time Frame
6 months from enrollment
Title
Change from baseline in mental functional status in 6 months
Description
Mental functional status is measured using the mental component score of the SF-12 scale
Time Frame
6 months from enrollment
Title
Change from baseline in physical functional status in 12 months
Description
Physical functional status is measured using the physical component score of the SF-12 scale
Time Frame
12 months from enrollment
Title
Change from baseline in mental functional status in 12 months
Description
Mental functional status is measured using the mental component score of the SF-12 scale
Time Frame
12 months after enrollment
Title
Change from baseline of mental health-related functional impairment in 12 months
Description
Assessed using the Sheehan disability scale
Time Frame
12 months from enrollment
Title
Change from baseline of mental health-related functional impairment in 6 months
Description
Assessed using the Sheehan disability scale
Time Frame
6 months from enrollment
Title
Change from baseline in depression outcome in 12 months
Description
Depression is measured using depression scales Patient Health Questionnaire (PHQ)-9. Major depression is classified as PHQ-9>=10.
Time Frame
12 months from enrollment
Title
Change from baseline in diabetes self-care score in 12 months
Description
Diabetes self-care is measured using Toolbert diabetes self-care scale.
Time Frame
12 months after enrollment
Title
Change from baseline of diabetes symptoms in 12 months
Description
Assessed using the Whitty-9 diabetes symptoms scale
Time Frame
12 months from enrollment
Title
Change from baseline of diabetes symptoms in 6 months
Description
Assessed using the Whitty-9 diabetes symptoms scale
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients who receive HbA1C lab test in 12 months
Description
This is one of our diabetes care processes measure. We are going to analyze the percentage of patients who receive the requisite lab tests, including HbA1C, microalbumin, and lipid panel.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients who receive the lipid panel lab test in 12 months
Description
This is one of our diabetes care processes measure. We are going to analyze the percentage of patients who receive the requisite lab tests, including HbA1C, microalbumin, and lipid panel.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients who receive microalbumin lab test in 12 months
Description
This is one of our diabetes care processes measure. We are going to analyze the percentage of patients who receive the requisite lab tests, including HbA1C, microalbumin, and lipid panel.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients who receive HbA1C lab test in 6 months
Description
This is one of our diabetes care processes measure. We are going to analyze the percentage of patients who receive the requisite lab tests, including HbA1C, microalbumin, and lipid panel.
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients who receive the lipid panel lab test in 6 months
Description
This is one of our diabetes care processes measure. We are going to analyze the percentage of patients who receive the requisite lab tests, including HbA1C, microalbumin, and lipid panel
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients who receive microalbumin lab test in 6 months
Description
This is one of our diabetes care processes measure. We are going to analyze the percentage of patients who receive the requisite lab tests, including HbA1C, microalbumin, and lipid panel.
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients whose HbA1C is in control in 12 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose HbA1C is in control pre- and post-intervention. HbA1C is considered controlled if it is <7%.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients whose microalbumin is in control in 12 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose microalbumin is in control pre- and post-intervention. Microalbumin is considered controlled if it is <30 microg/mg.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients whose total cholesterol is in control in 12 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose total cholesterol is in control pre- and post-intervention. Total cholesterol is considered controlled if it is <200mg/dL.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients whose LDL cholesterol is in control in 12 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose LDL cholesterol is in control pre- and post-intervention. LDL cholesterol is considered controlled if it is <100mg/dL.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients whose HDL cholesterol is in control in 12 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose HDL cholesterol is in control pre- and post-intervention. HDL cholesterol is considered controlled if it is <40mg/dL.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients whose triglycerides is in control in 12 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose triglycerides is in control pre- and post-intervention. Triglycerides is considered controlled if it is >200mg/dL.
Time Frame
12 months from enrollment
Title
Change from baseline in percentage of patients whose HbA1C is in control in 6 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose HbA1C is in control pre- and post-intervention. HbA1C is considered controlled if it is <7%.
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients whose microalbumin is in control in 6 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose microalbumin is in control pre- and post-intervention. Microalbumin is considered controlled if it is <20mg/L.
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients whose total cholesterol is in control in 6 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose total cholesterol is in control pre- and post-intervention. Total cholesterol is considered controlled if it is >240mg/dL
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients whose LDL cholesterol is in control in 6 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose LDL cholesterol is in control pre- and post-intervention. LDL cholesterol is considered controlled if it is >160mg/dL.
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients whose HDL cholesterol is in control in 6 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose HDL cholesterol is in control pre- and post-intervention. HDL cholesterol is considered controlled if it is >60mg/dL.
Time Frame
6 months from enrollment
Title
Change from baseline in percentage of patients whose triglycerides is in control in 6 months
Description
This is part of our diabetes outcome measure. We would like to know the percentage of patients whose triglycerides is in control pre- and post-intervention. Triglycerides is considered controlled if it is <150mg/dL
Time Frame
6 months from enrollment
Title
Change from baseline to 12 months in number of outpatient visits during the past 6 months
Description
This is part of our utilization measure. We would like to know the number of outpatient visits during 6-months before baseline and between 6- and 12-months after enrollment.
Time Frame
12 months from enrollment
Title
Change from baseline to 6 months in number of outpatient visits during the past 6 months
Description
This is part of our utilization measure. We would like to know the number of outpatient visits during 6-months before baseline and during the 6-months after enrollment.
Time Frame
6 months from enrollment
Title
Change from baseline to 12 months in percentage of patients who were hospitalized during the past 6 months
Description
This is part of our utilization measure. We would like to know the percentage of hospitalized patients during 6-months before baseline and between 6- and 12-months after enrollment.
Time Frame
12 months from enrollment
Title
Change from baseline to 6 months in percentage of hospitalized patients during the past 6 months
Description
This is part of our utilization measure. We would like to know the percentage of hospitalized patients during 6-months before baseline and during the 6-months after enrollment.
Time Frame
6 months from enrollment
Title
Change from baseline to 12 months in percentage of patients with ER visits during the past 6 months
Description
This is part of our utilization measure. We would like to know the percentage of patients with ER visits during 6-months before baseline and between 6- and 12-months after enrollment.
Time Frame
12 months from enrollment
Title
Change from baseline to 6 months in percentage of patients with ER visits during the past 6 months
Description
This is part of our utilization measure. We would like to know the percentage of patients with ER visits during 6-months before baseline and during the 6-months after enrollment.
Time Frame
6 months from enrollment
Title
Difference between cost of care management in the intervention group and the control groups over a 12-month period per patient
Description
Cost of care management includes automated phone calls, provider time, costs associated with reviewing tasks and follow-ups.
Time Frame
12 months
Title
Change from baseline to 12 months in percentage of patients satisfied with care received for diabetes
Description
Measured by the percentage of patients who answered "satisfied" or "very satisfied" to the question "How satisfied / dissatisfied are you with the overall health care available to you for your diabetes?" (with a 5-point Likert scale response option)
Time Frame
12 months from enrollment
Title
Change from baseline to 6 months in percentage of patients satisfied with care received for diabetes
Description
Measured by the percentage of patients who answered "satisfied" or "very satisfied" to the question "How satisfied / dissatisfied are you with the overall health care available to you for your diabetes?" (with a 5-point Likert scale response option)
Time Frame
6 months from enrollment
Title
Change from baseline to 12 months in percentage of patients satisfied with care received for depression
Description
Measured by the percentage of patients who answered "satisfied" or "very satisfied" to the question "How satisfied / dissatisfied are you with the clinical help received with your emotional problem?" (with a 5-point Likert scale response option)
Time Frame
12 months from enrollment
Title
Change from baseline to 6 months in percentage of patients satisfied with care received for depression
Description
Measured by the percentage of patients who answered "satisfied" or "very satisfied" to the question "How satisfied / dissatisfied are you with the clinical help received with your emotional problem?" (with a 5-point Likert scale response option)
Time Frame
6 months from enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age equal to or greater than 18 years receiving primary care at DHS safety net clinics having a current diagnosis of type 2 diabetes mellitus (non-gestational). have a working telephone or cellular phone. Exclusion Criteria: current suicidal ideation; inability to speak either English or Spanish; a score of 2 or greater on the CAGE (4M) alcohol assessment; having schizophrenia, schizoaffective disorder, manic-depressive, or needing lithium; and cognitive impairment precluding ability to give informed consent or participating in the intervention, i.e., Short Portable Mental Status Questionnaire(SPMSQ) score of 6 or more errors. Provider and administrator inclusion criteria are: practicing or managing at one of the eight study sites; involved with diabetes or depression care No specific exclusion criteria will be applied to providers and administrators.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shinyi Wu, PhD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
El Monte Comprehensive Health Center
City
El Monte
State/Province
California
ZIP/Postal Code
91731
Country
United States
Facility Name
High Desert Comprehensive Health Center
City
Lancaster
State/Province
California
ZIP/Postal Code
93536
Country
United States
Facility Name
Long Beach Comprehensive Health Center
City
Long Beach
State/Province
California
ZIP/Postal Code
90813
Country
United States
Facility Name
H. Claude Hudson Comprehensive Health Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90007
Country
United States
Facility Name
Roybal Comprehensive Health Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90022
Country
United States
Facility Name
Olive View-UCLA Medical Center Diabetes Clinic
City
Sylmar
State/Province
California
ZIP/Postal Code
91342
Country
United States
Facility Name
Mid-Valley Comprehensive Health Center
City
Van Nuys
State/Province
California
ZIP/Postal Code
91405
Country
United States
Facility Name
Harbor Comprehensive Health Center
City
Wilmington
State/Province
California
ZIP/Postal Code
90744
Country
United States

12. IPD Sharing Statement

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Diabetes-Depression Care-management Adoption Trial

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