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Resilience Against Depression Disparities (Also Known as Resilience Education to Reduce Depression Disparities) (RADD)

Primary Purpose

Depressive Symptoms

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Resiliency Class
Resource for Services (RS)
Sponsored by
Bowen Chung, MD, MSHS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Depressive Symptoms focused on measuring Depression, Resilience, Minority health, Community-based participatory research, Lesbian, gay, bisexual, transgender, and intersex (LGBTI) health, Racial / ethnic health disparities, Patient-centered outcomes research, Comparative-effectiveness research

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age 18 or older
  2. moderately to severely depressed (PHQ-8≥10)
  3. Able to be contacted by phone (voice or text message), e-mail, or Facebook.
  4. English or Spanish speaker

Exclusion Criteria:

  1. Under age 18 years
  2. Not moderately to severely depressed (PHQ-8≤10)
  3. Does not currently have a phone, an email address, or a Facebook profile

Sites / Locations

  • R.O.A.D.S. Clinic
  • The ADAM Project - YMSM Program
  • The LGBTQ Center - Long Beach
  • AMAAD
  • AIDS Health Foundation Healthcare Center - Downtown Los Angeles
  • AIDS Health Foundation Healthcare Center - Hollywood
  • AIDS Health Foundation Public Health Division
  • Metropolitan Community Church
  • OASIS Clinic
  • Southern Transmasculine Alliance
  • New Orleans Musicians Clinic
  • St. Anna's Church
  • Crescent Care - The Community Awareness Network (CAN Office)
  • Crescent City Sanctuary
  • Metropolitan Community Church of New Orleans
  • NOAGE
  • Brotherhood
  • Crescent Care - The Movement
  • Crescent Care
  • Odyssey Home
  • Sisters of Perpetual Indulgence - The Big Easy Sisters
  • Women with a Vision

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Resources for Services

Resiliency Class +

Arm Description

Resources for Services (RS) is an evidence-based depression QI toolkit developed for primary care, but adapted for health- and community-based programs. Protocols support training licensed providers in clinical assessment, medication management, and CBT; all staff in team management; and non-clinical staff in addressing patient safety, screening, behavioral management skills (behavioral activation, problem solving) to enable education, coordination, and referral. RS is offered as an initial 1-day / 8-hour training with follow-up through 12 webinars, 3 each on team management, medication management, psychotherapy, and case management. Programs will be invited to have a staff lead per training component, with no limit on number of staff at trainings. Training experts include a psychiatrist, psychologist/CBT trainer, case manager, support staff, and patient / community advocate liaison. All enrolled study participants will be nested within programs participating in RS.

Resiliency Classes (RC) are a manualized, 7-session, CBT, psychoeducation class, lead by community health workers, that teaches skills to enhance mood. The RC manual covers: Session 1 - "What Affects Your Mood and Resilience;" Session 2 - "Pleasant Activities Can Help Improve Your Mood and Make You Resilient;" Session 3 - "What Gets In The Way of Pleasant Activities: Harmful Thoughts and How to Change Them;" Session 4 - "How to Increase Your Resilience Through Support from Others;" Session 5 - "My Personal Resiliency Plan: Goal Setting;" Session 6 - "Celebrate Your Resiliency: Graduation" Each RC will be 90-120 minutes in duration; once a week in community settings with up to 10 participants. RC will be supplemented with automated mobile text reminders about basic concepts and follow-up for care. Half of enrolled participants will be randomized to the Resiliency Class +. As of July 12, 2018, we will be offering bus tokens and $5 for completion of a satisfaction survey.

Outcomes

Primary Outcome Measures

Depressive symptom count as measured by the Patient Health Questionnaire 8
The 8-item Patient Health Questionnaire (PHQ-8) is a standard measure of depressive symptoms.

Secondary Outcome Measures

Poor Mental Health-Related Quality of Life
12-item mental composite score (MCS-12) ≤ 40
Resilience
Brief Resilience Scale
Physical health-related quality of life
12-item physical composite score (PCS-12)
Mental Wellness
3 items in last 4 weeks: some feeling of being calm or peaceful, having energy or being happy (from 36-item Short Form Health Survey)

Full Information

First Posted
December 2, 2016
Last Updated
August 13, 2018
Sponsor
Bowen Chung, MD, MSHS
Collaborators
Louisiana State University Health Sciences Center in New Orleans, Tulane University, Healthy African American Families II, University of California, San Francisco, Arming Minorities Against Addiction & Disease, Louisiana Community Health Outreach Network
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1. Study Identification

Unique Protocol Identification Number
NCT02986126
Brief Title
Resilience Against Depression Disparities (Also Known as Resilience Education to Reduce Depression Disparities)
Acronym
RADD
Official Title
Resilience Against Depression Disparities (Also Known as Resilience Education to Reduce Depression Disparities)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
May 4, 2017 (Actual)
Primary Completion Date
August 1, 2019 (Anticipated)
Study Completion Date
November 1, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Bowen Chung, MD, MSHS
Collaborators
Louisiana State University Health Sciences Center in New Orleans, Tulane University, Healthy African American Families II, University of California, San Francisco, Arming Minorities Against Addiction & Disease, Louisiana Community Health Outreach Network

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
Depressive symptoms and disorders are among the most common adult health conditions with a lifetime prevalence of 15-20% and are a leading cause of disability /morbidity worldwide. Although evidence-based approaches such as cognitive behavioral therapy (CBT), antidepressant medications, and depression collaborative care and quality improvement (QI) programs integrating depression care into primary health care can improve depression outcomes and disparities, racial / ethnic disparities continue to persist. Concurrently, according to a 2011 Institute of Medicine (IOM) report, little information exists on how to address the high rates of depression among sexual and gender minorities. Our study randomizes depressed, LGBTQ (lesbian, gay, bisexual, transgendered, queer), racial / ethnic minority adults to an evidence-based agency-level, depression quality improvement (QI) training [Resources for Services (RS)] and technical support alone or to a resiliency class (RC+), a 7-session resiliency, cognitive behavioral therapy class to enhance mood + automated mobile text reminders about basic reminders and care follow-up impact on improving adult patients' depressive symptoms. Depression QI (RS) training will be offered to three clusters of four to five LGBTQ-focused programs: two clusters in LA (Hollywood and South LA) and one cluster in NO. Clusters are comprised of one primary care, one mental health, and two to three community agencies (e.g., faith-based, social services/support, advocacy). All programs will receive depression QI training. Enrolled adult depressed patients (n=320) will be randomized individually to RC+ or RS (depression QI) alone to assess effects on primary outcomes: depressive symptoms [8-item patient health questionnaire (PHQ-8) score and secondary outcomes: mental health quality of life [12-item mental composite score (MCS-12) ≤ 40], Resilience (Brief Resilience Scale), mental wellness, and physical health quality of life [12-item physical composite (PCS-12)score] at 6- and 12-month follow-up.
Detailed Description
Depressive symptoms and disorders are among the most common adult health conditions and are a leading cause of disability /morbidity worldwide. Although evidence-based approaches such as cognitive behavioral therapy (CBT), antidepressant medications, and depression collaborative care and quality improvement (QI) programs integrating depression care into primary health care can improve depression outcomes and disparities, racial / ethnic disparities continue to persist. Concurrently, according to a 2011 Institute of Medicine (IOM) report notes little information exists on how to address the high rates of depression among sexual and gender minorities, largely composed of lesbian, gay, and bisexual (LGBTQ) individuals. Limited comparative effectiveness data exists to know what treatments and services options improve health disparities due to patient characteristics such as race / ethnicity, and sexual orientation. "Resilience Against Depression Disparities (RADD)" randomizes enrolled depressed, LGBTQ, racial / ethnic minority adults (n=320) to an agency-level, evidence-based depression quality improvement (QI) intervention [Resources for Services (RS)] training and technical support and then randomizes individuals to Resources for Services alone or to Resiliency Class+, a 7-session resiliency, depression cognitive behavioral therapy class + automated mobile text reminders about basic reminders and care follow-up impact on improving adult patients' depressive symptoms over 6- and 12-months. RS training will be offered to three clusters of four to five LGBTQ-focused programs: two clusters in LA (Hollywood and South LA) and one cluster in NO. Clusters are comprised of one primary care, one mental health, and two to three community agencies (e.g., faith-based, social services/support, advocacy). All programs will receive RS (depression QI training). All enrolled adult depressed patients will be within programs participating in RS (depression QI) trainings. Half of enrolled participants will be randomized to the Resilience Class +.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Symptoms
Keywords
Depression, Resilience, Minority health, Community-based participatory research, Lesbian, gay, bisexual, transgender, and intersex (LGBTI) health, Racial / ethnic health disparities, Patient-centered outcomes research, Comparative-effectiveness research

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Resources for Services
Arm Type
Active Comparator
Arm Description
Resources for Services (RS) is an evidence-based depression QI toolkit developed for primary care, but adapted for health- and community-based programs. Protocols support training licensed providers in clinical assessment, medication management, and CBT; all staff in team management; and non-clinical staff in addressing patient safety, screening, behavioral management skills (behavioral activation, problem solving) to enable education, coordination, and referral. RS is offered as an initial 1-day / 8-hour training with follow-up through 12 webinars, 3 each on team management, medication management, psychotherapy, and case management. Programs will be invited to have a staff lead per training component, with no limit on number of staff at trainings. Training experts include a psychiatrist, psychologist/CBT trainer, case manager, support staff, and patient / community advocate liaison. All enrolled study participants will be nested within programs participating in RS.
Arm Title
Resiliency Class +
Arm Type
Active Comparator
Arm Description
Resiliency Classes (RC) are a manualized, 7-session, CBT, psychoeducation class, lead by community health workers, that teaches skills to enhance mood. The RC manual covers: Session 1 - "What Affects Your Mood and Resilience;" Session 2 - "Pleasant Activities Can Help Improve Your Mood and Make You Resilient;" Session 3 - "What Gets In The Way of Pleasant Activities: Harmful Thoughts and How to Change Them;" Session 4 - "How to Increase Your Resilience Through Support from Others;" Session 5 - "My Personal Resiliency Plan: Goal Setting;" Session 6 - "Celebrate Your Resiliency: Graduation" Each RC will be 90-120 minutes in duration; once a week in community settings with up to 10 participants. RC will be supplemented with automated mobile text reminders about basic concepts and follow-up for care. Half of enrolled participants will be randomized to the Resiliency Class +. As of July 12, 2018, we will be offering bus tokens and $5 for completion of a satisfaction survey.
Intervention Type
Behavioral
Intervention Name(s)
Resiliency Class
Intervention Description
See Arm Description
Intervention Type
Other
Intervention Name(s)
Resource for Services (RS)
Other Intervention Name(s)
Active Comparator
Intervention Description
See Resource for Services (RS) Description
Primary Outcome Measure Information:
Title
Depressive symptom count as measured by the Patient Health Questionnaire 8
Description
The 8-item Patient Health Questionnaire (PHQ-8) is a standard measure of depressive symptoms.
Time Frame
Change from baseline at 6- and 12-month follow-up
Secondary Outcome Measure Information:
Title
Poor Mental Health-Related Quality of Life
Description
12-item mental composite score (MCS-12) ≤ 40
Time Frame
6- and 12-month follow-up
Title
Resilience
Description
Brief Resilience Scale
Time Frame
6- and 12-month follow-up
Title
Physical health-related quality of life
Description
12-item physical composite score (PCS-12)
Time Frame
6- and 12-month follow-up
Title
Mental Wellness
Description
3 items in last 4 weeks: some feeling of being calm or peaceful, having energy or being happy (from 36-item Short Form Health Survey)
Time Frame
6- and 12-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 18 or older moderately to severely depressed (PHQ-8≥10) Able to be contacted by phone (voice or text message), e-mail, or Facebook. English or Spanish speaker Exclusion Criteria: Under age 18 years Not moderately to severely depressed (PHQ-8≤10) Does not currently have a phone, an email address, or a Facebook profile
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bowen Chung, MD, MSHS
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
R.O.A.D.S. Clinic
City
Compton
State/Province
California
ZIP/Postal Code
90221
Country
United States
Facility Name
The ADAM Project - YMSM Program
City
Long Beach
State/Province
California
ZIP/Postal Code
90806
Country
United States
Facility Name
The LGBTQ Center - Long Beach
City
Long Beach
State/Province
California
ZIP/Postal Code
90814
Country
United States
Facility Name
AMAAD
City
Los Angeles
State/Province
California
ZIP/Postal Code
90002
Country
United States
Facility Name
AIDS Health Foundation Healthcare Center - Downtown Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90015
Country
United States
Facility Name
AIDS Health Foundation Healthcare Center - Hollywood
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
AIDS Health Foundation Public Health Division
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
Metropolitan Community Church
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
OASIS Clinic
City
Los Angeles
State/Province
California
ZIP/Postal Code
90059
Country
United States
Facility Name
Southern Transmasculine Alliance
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70006
Country
United States
Facility Name
New Orleans Musicians Clinic
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70115
Country
United States
Facility Name
St. Anna's Church
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70116
Country
United States
Facility Name
Crescent Care - The Community Awareness Network (CAN Office)
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70117
Country
United States
Facility Name
Crescent City Sanctuary
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70118
Country
United States
Facility Name
Metropolitan Community Church of New Orleans
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70118
Country
United States
Facility Name
NOAGE
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70118
Country
United States
Facility Name
Brotherhood
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70119
Country
United States
Facility Name
Crescent Care - The Movement
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70119
Country
United States
Facility Name
Crescent Care
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70119
Country
United States
Facility Name
Odyssey Home
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70119
Country
United States
Facility Name
Sisters of Perpetual Indulgence - The Big Easy Sisters
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70119
Country
United States
Facility Name
Women with a Vision
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70119
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
We will work with the Patient-Centered Outcomes Research Institute (PCORI) staff as the findings emerge to determine the potential value of some or all of the dataset being made publicly available, which would require additional funding from PCORI to complete. In general PCORI works with investigators to make a complete, cleaned, de-identified final data set with detailed descriptions contained within the study protocol available to PCORI for use as a publicly available dataset after study completion.
Citations:
PubMed Identifier
17826170
Citation
Moussavi S, Chatterji S, Verdes E, Tandon A, Patel V, Ustun B. Depression, chronic diseases, and decrements in health: results from the World Health Surveys. Lancet. 2007 Sep 8;370(9590):851-8. doi: 10.1016/S0140-6736(07)61415-9.
Results Reference
result
PubMed Identifier
12837712
Citation
Miranda J, Chung JY, Green BL, Krupnick J, Siddique J, Revicki DA, Belin T. Treating depression in predominantly low-income young minority women: a randomized controlled trial. JAMA. 2003 Jul 2;290(1):57-65. doi: 10.1001/jama.290.1.57.
Results Reference
result
PubMed Identifier
10634337
Citation
Wells KB, Sherbourne C, Schoenbaum M, Duan N, Meredith L, Unutzer J, Miranda J, Carney MF, Rubenstein LV. Impact of disseminating quality improvement programs for depression in managed primary care: a randomized controlled trial. JAMA. 2000 Jan 12;283(2):212-20. doi: 10.1001/jama.283.2.212. Erratum In: JAMA 2000 Jun 28;283(24):3204.
Results Reference
result
PubMed Identifier
18522664
Citation
Wells KB, Tang L, Miranda J, Benjamin B, Duan N, Sherbourne CD. The effects of quality improvement for depression in primary care at nine years: results from a randomized, controlled group-level trial. Health Serv Res. 2008 Dec;43(6):1952-74. doi: 10.1111/j.1475-6773.2008.00871.x. Epub 2008 Jun 3.
Results Reference
result
PubMed Identifier
17130383
Citation
Gilbody S, Bower P, Fletcher J, Richards D, Sutton AJ. Collaborative care for depression: a cumulative meta-analysis and review of longer-term outcomes. Arch Intern Med. 2006 Nov 27;166(21):2314-21. doi: 10.1001/archinte.166.21.2314.
Results Reference
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PubMed Identifier
12785564
Citation
Miranda J, Duan N, Sherbourne C, Schoenbaum M, Lagomasino I, Jackson-Triche M, Wells KB. Improving care for minorities: can quality improvement interventions improve care and outcomes for depressed minorities? Results of a randomized, controlled trial. Health Serv Res. 2003 Apr;38(2):613-30. doi: 10.1111/1475-6773.00136.
Results Reference
result
PubMed Identifier
22013611
Citation
Institute of Medicine (US) Committee on Lesbian, Gay, Bisexual, and Transgender Health Issues and Research Gaps and Opportunities. The Health of Lesbian, Gay, Bisexual, and Transgender People: Building a Foundation for Better Understanding. Washington (DC): National Academies Press (US); 2011. Available from http://www.ncbi.nlm.nih.gov/books/NBK64806/
Results Reference
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PubMed Identifier
22352077
Citation
Springgate BF, Wennerstrom A, Meyers D, Allen CE 3rd, Vannoy SD, Bentham W, Wells KB. Building community resilience through mental health infrastructure and training in post-Katrina New Orleans. Ethn Dis. 2011 Summer;21(3 Suppl 1):S1-20-9.
Results Reference
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PubMed Identifier
23649787
Citation
Wells KB, Jones L, Chung B, Dixon EL, Tang L, Gilmore J, Sherbourne C, Ngo VK, Ong MK, Stockdale S, Ramos E, Belin TR, Miranda J. Community-partnered cluster-randomized comparative effectiveness trial of community engagement and planning or resources for services to address depression disparities. J Gen Intern Med. 2013 Oct;28(10):1268-78. doi: 10.1007/s11606-013-2484-3. Epub 2013 May 7. Erratum In: J Gen Intern Med. 2013 Nov;28(11):1534.
Results Reference
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PubMed Identifier
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Citation
Chung B, Ong M, Ettner SL, Jones F, Gilmore J, McCreary M, Sherbourne C, Ngo V, Koegel P, Tang L, Dixon E, Miranda J, Belin TR, Wells KB. 12-month outcomes of community engagement versus technical assistance to implement depression collaborative care: a partnered, cluster, randomized, comparative effectiveness trial. Ann Intern Med. 2014 Nov 18;161(10 Suppl):S23-34. doi: 10.7326/M13-3011.
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PubMed Identifier
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Citation
Chung B, Ngo VK, Ong MK, Pulido E, Jones F, Gilmore J, Stoker-Mtume N, Johnson M, Tang L, Wells KB, Sherbourne C, Miranda J. Participation in Training for Depression Care Quality Improvement: A Randomized Trial of Community Engagement or Technical Support. Psychiatr Serv. 2015 Aug 1;66(8):831-9. doi: 10.1176/appi.ps.201400099. Epub 2015 May 1.
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Citation
Katon WJ, Lin EH, Von Korff M, Ciechanowski P, Ludman EJ, Young B, Peterson D, Rutter CM, McGregor M, McCulloch D. Collaborative care for patients with depression and chronic illnesses. N Engl J Med. 2010 Dec 30;363(27):2611-20. doi: 10.1056/NEJMoa1003955.
Results Reference
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Citation
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PubMed Identifier
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Citation
Vargas SM, Wennerstrom A, Alfaro N, Belin T, Griffith K, Haywood C, Jones F, Lunn MR, Meyers D, Miranda J, Obedin-Maliver J, Pollock M, Sherbourne CD, Springgate BF, Sugarman OK, Rey E, Williams C, Williams P, Chung B. Resilience Against Depression Disparities (RADD): a protocol for a randomised comparative effectiveness trial for depression among predominantly low-income, racial/ethnic, sexual and gender minorities. BMJ Open. 2019 Oct 22;9(10):e031099. doi: 10.1136/bmjopen-2019-031099.
Results Reference
derived
Links:
URL
http://www.pcori.org/research-results/2016/resiliency-education-reduce-depression-disparities
Description
Patient-Centered Outcomes Research Institute Project Summary

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Resilience Against Depression Disparities (Also Known as Resilience Education to Reduce Depression Disparities)

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