Diabetes-Depression Care-management Adoption Trial (DCAT)

December 3, 2014 updated by: Shinyi Wu, University of Southern California

Care Management Technology to Facilitate Depression Care in Safety Net Diabetes Clinics

The specific aims of the proposed study are to:

  1. 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;
  2. Conduct the quasi-experiment in eight Los Angeles County Department of Health Services (LAC-DHS) clinics to test the interventions;
  3. 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
  4. 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:

  1. 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).

  2. 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.

  3. 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.

  4. 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.
  5. Of the three groups compared, the TC group will be the most cost-effective approach for accelerating adoption of the CER depression care results.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

In addition, the study will aim to answer the secondary research questions listed below:

  1. What is medical provider satisfaction with the technology used in the TC (Technology Care) group?
  2. What is patient acceptance with the technology used in the TC group?
  3. What factors are identified by medical providers and clinic administrators as related to satisfaction, barriers, and sustaining the intervention post-trial?
  4. What are patients' reported satisfaction and facilitating factors and barriers to receipt and acceptance of depression care?

Study Type

Interventional

Enrollment (Actual)

1485

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • El Monte, California, United States, 91731
        • El Monte Comprehensive Health Center
      • Lancaster, California, United States, 93536
        • High Desert Comprehensive Health Center
      • Long Beach, California, United States, 90813
        • Long Beach Comprehensive Health Center
      • Los Angeles, California, United States, 90007
        • H. Claude Hudson Comprehensive Health Center
      • Los Angeles, California, United States, 90022
        • Roybal Comprehensive Health Center
      • Sylmar, California, United States, 91342
        • Olive View-UCLA Medical Center Diabetes Clinic
      • Van Nuys, California, United States, 91405
        • Mid-Valley Comprehensive Health Center
      • Wilmington, California, United States, 90744
        • Harbor Comprehensive Health Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: HEALTH_SERVICES_RESEARCH
  • Allocation: NON_RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Technology-supported care
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.
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)..
NO_INTERVENTION: Supported-Care
This arm consists of CRM (Clinic Resource Management) clinics and serves as one of the two control arms in the study.
NO_INTERVENTION: Usual Care
This arm consists of non-CRM (Clinic Resource Management) clinics and serves as one of the two control arms in the study.

What is the study measuring?

Primary Outcome Measures

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

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in diabetes self-care score in 6 months
Time Frame: 6 months from enrollment
Diabetes self-care is measured using the Toolbert diabetes self-care scale.
6 months from enrollment

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in physical functional status in 6 months
Time Frame: 6 months from enrollment
Physical functional status is measured using the physical component score of the SF-12 scale
6 months from enrollment
Change from baseline in mental functional status in 6 months
Time Frame: 6 months from enrollment
Mental functional status is measured using the mental component score of the SF-12 scale
6 months from enrollment
Change from baseline in physical functional status in 12 months
Time Frame: 12 months from enrollment
Physical functional status is measured using the physical component score of the SF-12 scale
12 months from enrollment
Change from baseline in mental functional status in 12 months
Time Frame: 12 months after enrollment
Mental functional status is measured using the mental component score of the SF-12 scale
12 months after enrollment
Change from baseline of mental health-related functional impairment in 12 months
Time Frame: 12 months from enrollment
Assessed using the Sheehan disability scale
12 months from enrollment
Change from baseline of mental health-related functional impairment in 6 months
Time Frame: 6 months from enrollment
Assessed using the Sheehan disability scale
6 months from enrollment
Change from baseline in depression outcome in 12 months
Time Frame: 12 months from enrollment
Depression is measured using depression scales Patient Health Questionnaire (PHQ)-9. Major depression is classified as PHQ-9>=10.
12 months from enrollment
Change from baseline in diabetes self-care score in 12 months
Time Frame: 12 months after enrollment
Diabetes self-care is measured using Toolbert diabetes self-care scale.
12 months after enrollment
Change from baseline of diabetes symptoms in 12 months
Time Frame: 12 months from enrollment
Assessed using the Whitty-9 diabetes symptoms scale
12 months from enrollment
Change from baseline of diabetes symptoms in 6 months
Time Frame: 6 months from enrollment
Assessed using the Whitty-9 diabetes symptoms scale
6 months from enrollment
Change from baseline in percentage of patients who receive HbA1C lab test in 12 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline in percentage of patients who receive the lipid panel lab test in 12 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline in percentage of patients who receive microalbumin lab test in 12 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline in percentage of patients who receive HbA1C lab test in 6 months
Time Frame: 6 months from enrollment
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.
6 months from enrollment
Change from baseline in percentage of patients who receive the lipid panel lab test in 6 months
Time Frame: 6 months from enrollment
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
6 months from enrollment
Change from baseline in percentage of patients who receive microalbumin lab test in 6 months
Time Frame: 6 months from enrollment
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.
6 months from enrollment
Change from baseline in percentage of patients whose HbA1C is in control in 12 months
Time Frame: 12 months from enrollment
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%.
12 months from enrollment
Change from baseline in percentage of patients whose microalbumin is in control in 12 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline in percentage of patients whose total cholesterol is in control in 12 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline in percentage of patients whose LDL cholesterol is in control in 12 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline in percentage of patients whose HDL cholesterol is in control in 12 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline in percentage of patients whose triglycerides is in control in 12 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline in percentage of patients whose HbA1C is in control in 6 months
Time Frame: 6 months from enrollment
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%.
6 months from enrollment
Change from baseline in percentage of patients whose microalbumin is in control in 6 months
Time Frame: 6 months from enrollment
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.
6 months from enrollment
Change from baseline in percentage of patients whose total cholesterol is in control in 6 months
Time Frame: 6 months from enrollment
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
6 months from enrollment
Change from baseline in percentage of patients whose LDL cholesterol is in control in 6 months
Time Frame: 6 months from enrollment
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.
6 months from enrollment
Change from baseline in percentage of patients whose HDL cholesterol is in control in 6 months
Time Frame: 6 months from enrollment
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.
6 months from enrollment
Change from baseline in percentage of patients whose triglycerides is in control in 6 months
Time Frame: 6 months from enrollment
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
6 months from enrollment
Change from baseline to 12 months in number of outpatient visits during the past 6 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline to 6 months in number of outpatient visits during the past 6 months
Time Frame: 6 months from enrollment
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.
6 months from enrollment
Change from baseline to 12 months in percentage of patients who were hospitalized during the past 6 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline to 6 months in percentage of hospitalized patients during the past 6 months
Time Frame: 6 months from enrollment
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.
6 months from enrollment
Change from baseline to 12 months in percentage of patients with ER visits during the past 6 months
Time Frame: 12 months from enrollment
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.
12 months from enrollment
Change from baseline to 6 months in percentage of patients with ER visits during the past 6 months
Time Frame: 6 months from enrollment
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.
6 months from enrollment
Difference between cost of care management in the intervention group and the control groups over a 12-month period per patient
Time Frame: 12 months
Cost of care management includes automated phone calls, provider time, costs associated with reviewing tasks and follow-ups.
12 months
Change from baseline to 12 months in percentage of patients satisfied with care received for diabetes
Time Frame: 12 months from enrollment
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)
12 months from enrollment
Change from baseline to 6 months in percentage of patients satisfied with care received for diabetes
Time Frame: 6 months from enrollment
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)
6 months from enrollment
Change from baseline to 12 months in percentage of patients satisfied with care received for depression
Time Frame: 12 months from enrollment
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)
12 months from enrollment
Change from baseline to 6 months in percentage of patients satisfied with care received for depression
Time Frame: 6 months from enrollment
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)
6 months from enrollment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2010

Primary Completion (ACTUAL)

September 1, 2013

Study Completion (ACTUAL)

September 1, 2013

Study Registration Dates

First Submitted

January 29, 2013

First Submitted That Met QC Criteria

January 29, 2013

First Posted (ESTIMATE)

January 31, 2013

Study Record Updates

Last Update Posted (ESTIMATE)

December 5, 2014

Last Update Submitted That Met QC Criteria

December 3, 2014

Last Verified

December 1, 2014

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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