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Preventing Depression in Late Life: A Model for Low and Middle Income Countries

Primary Purpose

Depression, Anxiety Disorder

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Problem Solving therapy and Brief Behavioral Treatment of Insomnia
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Depression focused on measuring Prevention of depression and anxiety disorder, Depression Prevention

Eligibility Criteria

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

Inclusion Criteria:

  • Patient at the participating primary care centers
  • age 60 and older
  • GHQ scores 4 or above
  • Hindi MMSE scores 24 or higher
  • no episodes of major depression or anxiety disorder within the past 12 months
  • no current antidepressant pharmacotherapy

Exclusion Criteria:

  • episode of major depression or anxiety disorder within the past 12 months
  • current antidepressant pharmacotherapy
  • younger than age 60
  • Hindi MMSE scores less than 24
  • GHQ scores less than 4

Sites / Locations

  • Goa Medical College

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

problem solving therapy + Behavioral Treatment of Insomnia

Enhanced Usual Care

Arm Description

Problem Solving Therapy + Brief Behavioral Treatment of Insomnia as needed

Care as usual with scheduled assessments of clinical status

Outcomes

Primary Outcome Measures

Percent of Participants Who Develop Major Depression and Anxiety Disorders
Cumulative incidence of episodes of major depression and anxiety disorders over a 12-month period measured by MINI
General Health Questionnaire (GHQ) Scores
Levels of depressive and anxiety symptoms. Scores on the General Health Questionnaire (GHQ-12) range from 0 to 12; a higher score indicated greater symptoms for depression and anxiety

Secondary Outcome Measures

World Health Organization Disability Assessment Schedule (WHODAS-II) Scores
Assessment instrument for health and disability or functional status. Scores on the World Health Organization Disability Assessment Schedule (WHODAS 2.0) range from 12 to 60; a higher score indicated greater disability.

Full Information

First Posted
May 20, 2014
Last Updated
January 18, 2019
Sponsor
University of Pittsburgh
Collaborators
National Institutes of Health (NIH), Goa Medical College, Sangath
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1. Study Identification

Unique Protocol Identification Number
NCT02145429
Brief Title
Preventing Depression in Late Life: A Model for Low and Middle Income Countries
Official Title
Preventing Depression in Late Life: A Model for Low and Middle Income Countries
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
September 2013 (Actual)
Primary Completion Date
November 7, 2018 (Actual)
Study Completion Date
November 7, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
National Institutes of Health (NIH), Goa Medical College, Sangath

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is being conducted in GOA India. The study addresses specific issues of depression prevention in older adults living in low- and middle income countries (LMICs), by developing risk-reduction strategies through the use of lay health counselors. We will be training Lay Health Counselors (LHC's) to deliver simple behaviorally oriented interventions, designed to enhance the ability to relax, to improve active coping via better problem solving, and to increase protective factors such as good quality sleep. Lay Health Counselors are inhabitants of Goa. The aim of phase 1 is to create a depression and anxiety prevention intervention for use by lay health counselors. We will test the feasibility and acceptability of Problem Solving Therapy for Primary Care (PST-PC) and Brief Behavioral Treatment for Insomnia (BBTI). The products of phase 1 will be a prevention and counseling manual to standardize the implementation of the interventions for further testing in a randomized prevention trial (Specific Aim 2) and the adaptation of PST-PC and BBTI for the Indian population. In Phase 2, we will: gather data on the feasibility of identifying, enrolling, randomizing and retaining participants; implement the experimental intervention and enhanced usual care; identify "real world", barriers and develop strategies for addressing them; and assess the fidelity of the interventions.
Detailed Description
Prevention of common mental disorders in older adults (major depression and anxiety disorders) in Low and Middle Income Countries (LMICs) is a major challenge in global mental health research. The public health imperative for devising strategies to prevent late life depression and anxiety in LMICs includes the rapid demographic transition and aging in countries like India, increased exposure of older adults to risk factors for depression (disability, depletion of economic and social resources, bereavement, care giving, and chronic insomnia), and workforce issues (such as a dearth of mental health specialists). The dearth of specialist resources, together with the limited ability of current depression treatments to avert years lived with disability, underscores the need for preventive interventions that can be delivered by lay health workers in non-health care or primary care settings. Such development could also benefit policy and practice in the US by clarifying appropriate roles for lay and non-specialist workers in depression and anxiety prevention for populations with few mental health resources. We propose to build upon the MANAS trial conducted in Goa, India. Given the shortage of mental health specialists in Low and Middle Income Countries (LMICs), MANAS (which means "project to promote mental health" in the Konkani language) employed the strategy of task-shifting, that is, the rational redistribution of tasks among health workforce teams to make more efficient use of lay human resources for health. MANAS demonstrated that the use of lay health counselors (LHCs), as part of a collaborative stepped care intervention, increases rates of recovery from common mental disorders (depression and anxiety) in public primary care facilities. In addition, preliminary evidence indicated that the MANAS model of using Lay Health Counselors in a stepped-care collaborative intervention may also reduce the incidence of common mental disorders in those who initially present with subthreshold (subsyndromal) depressive and anxiety symptoms. We propose to investigate translation of depression and anxiety prevention strategies to LMICs through non-specialist delivery systems. The goal of this study is to develop and pilot test in Goa, India a Lay Health Counselor-led depression and anxiety disorder prevention strategy, building upon the experience of the MANAS treatment trial called the DIL (Depression in Late Life) intervention. Specific Aim (1) formative research (months 1 - 12): following Medical Research Council Guidelines for the development of complex interventions, we will create and standardize a MANAS-derived depression and anxiety prevention intervention (DIL Intervention) for use by lay health counselors (LHCs) in primary care clinics in Goa. We will develop an intervention manual based on the original MANAS trial and best practices for depression and anxiety prevention from the global literature. Via systematic study of an uncontrolled case series (enrolling 20 subjects), we will test the feasibility and acceptability of DIL Intervention. The DIL Intervention will comprise psychoeducational interventions delivered by Lay Health Counselors and previously shown to have prevention, such as Problem Solving Therapy for Primary Care (PST-PC) and Brief Behavioral Treatment for Insomnia (BBTI). The products of Specific Aim (1) will be a prevention manual to standardize the implementation of DIL Intervention for further testing in a pilot randomized prevention trial (Specific Aim 2), together with recruitment and assessment protocols and a randomization procedure. Specific Aim (2) pilot randomized prevention trial (months 13 - 36): Via the use of a pilot randomized prevention trial (DIL Intervention) we will: gather data on the feasibility of identifying, enrolling, randomizing and retaining participants; implement the experimental intervention and enhanced usual care; identify "real world", barriers and develop strategies for addressing them; and assess the fidelity of the DIL implementation. As recommended in the R34 program announcement (PAR-09-173), we will collect measures of feasibility, acceptability, tolerability, and safety, rather than conducting formal tests of outcome or attempting to obtain an estimate of an effect size (because estimates are likely to be inflated and unstable.) These data will be critical to a subsequent confirmatory randomized depression prevention trial based in Goa and to our long-term goal of scalable depression prevention in Low and Middle Income Countries (LMICs).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Anxiety Disorder
Keywords
Prevention of depression and anxiety disorder, Depression Prevention

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
problem solving therapy + Behavioral Treatment of Insomnia
Arm Type
Experimental
Arm Description
Problem Solving Therapy + Brief Behavioral Treatment of Insomnia as needed
Arm Title
Enhanced Usual Care
Arm Type
No Intervention
Arm Description
Care as usual with scheduled assessments of clinical status
Intervention Type
Behavioral
Intervention Name(s)
Problem Solving therapy and Brief Behavioral Treatment of Insomnia
Intervention Description
Problem Solving therapy teaches problem solving skills that participants can use in their everyday life. A problem is identified, various solutions identified and explored with the underlying focus to learn behavioral and self management strategies.Social casework and management of chronic disease is also included as per the participant's need. Brief Behavioral Treatment of Insomnia focuses on improving sleep by promoting sleep hygiene such as time spent in bed and decreasing night time stimuli. The therapy has been suitably modified to suit the needs of the participants to be recruited in the Low and Middle income countries keeping in mind the low level of literacy and the local social and health care services.
Primary Outcome Measure Information:
Title
Percent of Participants Who Develop Major Depression and Anxiety Disorders
Description
Cumulative incidence of episodes of major depression and anxiety disorders over a 12-month period measured by MINI
Time Frame
One year
Title
General Health Questionnaire (GHQ) Scores
Description
Levels of depressive and anxiety symptoms. Scores on the General Health Questionnaire (GHQ-12) range from 0 to 12; a higher score indicated greater symptoms for depression and anxiety
Time Frame
One year
Secondary Outcome Measure Information:
Title
World Health Organization Disability Assessment Schedule (WHODAS-II) Scores
Description
Assessment instrument for health and disability or functional status. Scores on the World Health Organization Disability Assessment Schedule (WHODAS 2.0) range from 12 to 60; a higher score indicated greater disability.
Time Frame
One year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient at the participating primary care centers age 60 and older GHQ scores 4 or above Hindi MMSE scores 24 or higher no episodes of major depression or anxiety disorder within the past 12 months no current antidepressant pharmacotherapy Exclusion Criteria: episode of major depression or anxiety disorder within the past 12 months current antidepressant pharmacotherapy younger than age 60 Hindi MMSE scores less than 24 GHQ scores less than 4
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles F Reynolds, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Amit Dias, MD
Organizational Affiliation
Sangath and Goa College of Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Vikram Patel, MD, PHD
Organizational Affiliation
Sangath
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alex Cohen, PhD
Organizational Affiliation
London School of Hygiene and Tropical Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Goa Medical College
City
Bambolim
State/Province
Goa
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
30422259
Citation
Dias A, Azariah F, Anderson SJ, Sequeira M, Cohen A, Morse JQ, Cuijpers P, Patel V, Reynolds CF 3rd. Effect of a Lay Counselor Intervention on Prevention of Major Depression in Older Adults Living in Low- and Middle-Income Countries: A Randomized Clinical Trial. JAMA Psychiatry. 2019 Jan 1;76(1):13-20. doi: 10.1001/jamapsychiatry.2018.3048.
Results Reference
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Preventing Depression in Late Life: A Model for Low and Middle Income Countries

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