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Critical Time Intervention-Task Shifting: Randomized Controlled Trial (CTI-TS RCT)

Primary Purpose

Schizophrenia, Psychotic Disorder

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
CTI-TS
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Schizophrenia focused on measuring Schizophrenia and Disorders with Psychotic Features, Community Psychiatry

Eligibility Criteria

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

Inclusion Criteria:

  • 21-65 years of age.
  • No longer than 6 months since the first visit to the MHS (excluding visits that took place more than one year ago).
  • Any psychotic disorder (chart diagnosis) from the following groups (ICD-10 criteria):

F20-29 including schizophrenia, delusional disorders, schizotypal disorders, acute polymorph psychotic disorders, schizoaffective disorders

F30-39 the following mood [affective] disorders with psychoses:

F30.2 Mania with psychotic symptoms F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms F31.5 Bipolar affective disorder, current episode severe depression with psychotic symptoms F32.3 Severe depressive episode with psychotic symptoms F33.3 Recurrent depressive disorder, current episode severe with psychotic symptom

Exclusion Criteria:

  • Under age 21 or over age 65.
  • Active suicidal ideation.
  • Substance Abuse or Dependence alone (may have psychotic symptoms but does not meet criteria for diagnoses included).
  • Serious cognitive or other sensorial impairment which is likely to preclude reliable assessment via our interview procedures.

Sites / Locations

  • Federal University of Rio de Janeiro
  • University of Chile

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

CTI-TS

Usual Care

Arm Description

CTI-TS is a time-limited, 9-month long intervention, provided at the critical time when a person is first offered services at a mental health clinic, or, at the similarly critical time when a person first seeks to reconnect with a mental health clinic after a long lapse.

The Usual Care group will receive mental health services as provided by the local mental health services clinic.

Outcomes

Primary Outcome Measures

Camberwell Assessment of Need (CAN)
Used to assess the needs of people with severe mental illness.
World Health Organization Quality of Life, Short Form (WHOQOL-BREF)
Used to provide a quality of life measurement.

Secondary Outcome Measures

World Health Organization Disability Assessment Schedule II (WHODAS 2.0)
Measures level of disability
Recovery Assessment Scale (RAS)
Assessment tool to measure factors important to recovery
Continuity of care and course of illness
CONNECT, a measure of continuity of care, and the Life Chart Schedule are used.
Perceived stigma
Perceived Discrimination and Devaluation Scale (PDD) is used for this outcome
Self-stigma
Internalized stigma of mental illness (ISMI) is the measure used.
Substance use
ASSIST, the WHO Alcohol, Smoking and Substance Involvement Screening Test is used for this measure.

Full Information

First Posted
November 18, 2013
Last Updated
June 23, 2020
Sponsor
Columbia University
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT01995864
Brief Title
Critical Time Intervention-Task Shifting: Randomized Controlled Trial
Acronym
CTI-TS RCT
Official Title
A Pilot Multi-center Randomized Controlled Trial of Critical Time Intervention - Task Shifting (CTI-TS) Versus Usual Care for People With Psychotic Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
February 2014 (Actual)
Primary Completion Date
June 1, 2020 (Actual)
Study Completion Date
June 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
Collaborators
National Institute of Mental Health (NIMH)

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
The study represents the research component of a broader initiative entitled "RedeAmericas". RedeAmericas (RA) is a collaborative effort of investigators from six cities across Latin America (Buenos Aires, Cordoba, Medellin, Neuquen, Rio de Janeiro, and Santiago) and Columbia University in New York. This is a pilot Randomized Controlled Trial (RCT) of Critical Time Intervention-Task Shifting (CTI-TS). It is designed to address a fundamental gap in the services offered by mental health clinics. These clinics are the primary locale for outpatient treatment of individuals with severe mental disorders in the urban areas of Latin America, and they offer some basic and important clinical care such as pharmacologic treatment onsite. Generally these clinics also have a major limitation; they have inadequate resources and training for the provision of in vivo community-based services, that is, services delivered outside of the clinic facility in homes or elsewhere in the community. In most urban areas, they also have weak links to primary health care and are not easily accessible to much of the population. CTI-TS, is a task shifting intervention that at the service user level provides support for better community living and promotes social integration, and at the system level strengthens the connections between mental health and primary care clinics. CTI-TS is a time-limited 9-month intervention provided at the critical time when a person is first offered services at a mental health clinic. During this period CTI-TS workers forge relationships that will shape the continuing use of services and enhance the potential for recovery over the subsequent course of time. The overall goal of CTI-TS is to improve the lives of those with severe mental disorders who receive community-based mental health care.
Detailed Description
Critical Time Intervention-Task Shifting (CTI-TS)is delivered by lay Community Mental Health Workers (CMHWs) and Peer Support Workers (PSWs) based in mental health outpatient service programs (MHS) and supervised by mental health professionals. These workers provide community outreach and support to engage service users, their families, primary care practitioners, peers and other community members in the recovery process. The CTI-TS program is concerned with improving supports for people recovering from episodes of mental illness. Examples of areas where extra support may be provided include medication management, housing or crisis management, help with the family, help obtaining good services from mental health centers and primary health centers, and help developing social relationships in the community. The program is provided by a CTI-TS team, including a community mental health worker and a peer support worker (someone who has used mental health services in the past, and has recovered). All of the CTI-TS activities will last 9 months. The evaluation of how people fare will last 18 months. The activities of CTI-TS will be in addition to the usual care provided by the subject's local health service. Usual care might include meeting with a mental health professional, meeting with a social worker, and/or obtaining prescriptions for medicine. This study will compare how people fare who have participated in the CTI-TS activities against the group of people who received only the regular services of this community mental health center. As part of the study, a trained researcher will meet with each subject for an interview at the beginning of the project, again 9 months later, and again after 18 months. These interviews will ask questions about how the subject is doing with his/her health and quality of life, and if the subject is getting help or support with problems.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Psychotic Disorder
Keywords
Schizophrenia and Disorders with Psychotic Features, Community Psychiatry

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CTI-TS
Arm Type
Experimental
Arm Description
CTI-TS is a time-limited, 9-month long intervention, provided at the critical time when a person is first offered services at a mental health clinic, or, at the similarly critical time when a person first seeks to reconnect with a mental health clinic after a long lapse.
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
The Usual Care group will receive mental health services as provided by the local mental health services clinic.
Intervention Type
Behavioral
Intervention Name(s)
CTI-TS
Other Intervention Name(s)
CTI-TS (Critical Time Intervention-Task Shifting)
Intervention Description
The following briefly describes the three phases of CTI-TS: Phase 1: Initiation: The client and CTI-TS team formulate a treatment plan that focuses on selected areas identified as crucial for strengthening stability and facilitating the assimilation of the individual into community living. Phase 2: The Try-Out phase is devoted to testing and adjusting the support systems that have been established in the community. Phase 3: The final phase, Transfer of Care, is devoted to making any necessary improvements in the network of supports of the individual.
Primary Outcome Measure Information:
Title
Camberwell Assessment of Need (CAN)
Description
Used to assess the needs of people with severe mental illness.
Time Frame
18 months
Title
World Health Organization Quality of Life, Short Form (WHOQOL-BREF)
Description
Used to provide a quality of life measurement.
Time Frame
18 months
Secondary Outcome Measure Information:
Title
World Health Organization Disability Assessment Schedule II (WHODAS 2.0)
Description
Measures level of disability
Time Frame
18 months
Title
Recovery Assessment Scale (RAS)
Description
Assessment tool to measure factors important to recovery
Time Frame
18 months
Title
Continuity of care and course of illness
Description
CONNECT, a measure of continuity of care, and the Life Chart Schedule are used.
Time Frame
18 months
Title
Perceived stigma
Description
Perceived Discrimination and Devaluation Scale (PDD) is used for this outcome
Time Frame
18 months
Title
Self-stigma
Description
Internalized stigma of mental illness (ISMI) is the measure used.
Time Frame
18 months
Title
Substance use
Description
ASSIST, the WHO Alcohol, Smoking and Substance Involvement Screening Test is used for this measure.
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 21-65 years of age. No longer than 6 months since the first visit to the MHS (excluding visits that took place more than one year ago). Any psychotic disorder (chart diagnosis) from the following groups (ICD-10 criteria): F20-29 including schizophrenia, delusional disorders, schizotypal disorders, acute polymorph psychotic disorders, schizoaffective disorders F30-39 the following mood [affective] disorders with psychoses: F30.2 Mania with psychotic symptoms F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms F31.5 Bipolar affective disorder, current episode severe depression with psychotic symptoms F32.3 Severe depressive episode with psychotic symptoms F33.3 Recurrent depressive disorder, current episode severe with psychotic symptom Exclusion Criteria: Under age 21 or over age 65. Active suicidal ideation. Substance Abuse or Dependence alone (may have psychotic symptoms but does not meet criteria for diagnoses included). Serious cognitive or other sensorial impairment which is likely to preclude reliable assessment via our interview procedures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ezra Susser, MD, DrPH
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Graciela Rojas, MD
Organizational Affiliation
University of Chile
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sandro Galea, MD DrPH
Organizational Affiliation
Boston University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ruben Alvarado, MD PhD
Organizational Affiliation
University of Chile
Official's Role
Principal Investigator
Facility Information:
Facility Name
Federal University of Rio de Janeiro
City
Rio de Janeiro
Country
Brazil
Facility Name
University of Chile
City
Santiago
Country
Chile

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23990755
Citation
Yang LH, Valencia E, Alvarado R, Link B, Huynh N, Nguyen K, Morita K, Saavedra M, Wong C, Galea S, Susser E. A theoretical and empirical framework for constructing culture-specific stigma instruments for Chile. Cad Saude Colet. 2013;21(1):71-79. doi: 10.1590/s1414-462x2013000100011.
Results Reference
background
PubMed Identifier
22794167
Citation
Baumgartner JN, Susser E. Social integration in global mental health: what is it and how can it be measured? Epidemiol Psychiatr Sci. 2013 Mar;22(1):29-37. doi: 10.1017/S2045796012000303. Epub 2012 May 25.
Results Reference
background
PubMed Identifier
25339792
Citation
Minoletti A, Galea S, Susser E. Community Mental Health Services in Latin America for People with Severe Mental Disorders. Public Health Rev. 2012;34(2):http://www.publichealthreviews.eu/show/a/116. doi: 10.1007/BF03391681.
Results Reference
background
PubMed Identifier
10749277
Citation
Herman D, Opler L, Felix A, Valencia E, Wyatt RJ, Susser E. A critical time intervention with mentally ill homeless men: impact on psychiatric symptoms. J Nerv Ment Dis. 2000 Mar;188(3):135-40. doi: 10.1097/00005053-200003000-00002.
Results Reference
background
PubMed Identifier
12773605
Citation
Jones K, Colson PW, Holter MC, Lin S, Valencia E, Susser E, Wyatt RJ. Cost-effectiveness of critical time intervention to reduce homelessness among persons with mental illness. Psychiatr Serv. 2003 Jun;54(6):884-90. doi: 10.1176/appi.ps.54.6.884.
Results Reference
background
PubMed Identifier
21724782
Citation
Herman DB, Conover S, Gorroochurn P, Hinterland K, Hoepner L, Susser ES. Randomized trial of critical time intervention to prevent homelessness after hospital discharge. Psychiatr Serv. 2011 Jul;62(7):713-9. doi: 10.1176/ps.62.7.pss6207_0713.
Results Reference
background
PubMed Identifier
9103106
Citation
Susser E, Valencia E, Conover S, Felix A, Tsai WY, Wyatt RJ. Preventing recurrent homelessness among mentally ill men: a "critical time" intervention after discharge from a shelter. Am J Public Health. 1997 Feb;87(2):256-62. doi: 10.2105/ajph.87.2.256.
Results Reference
background
PubMed Identifier
30791796
Citation
Agrest M, Le PD, Yang LH, Mascayano F, Alves-Nishioka S, Dev S, Kankan T, Tapia-Munoz T, Sawyer S, Toso-Salman J, Dishy GA, Jorquera MJ, Schilling S, Pratt C, Price L, Valencia E, Conover S, Alvarado R, Susser ES. Implementing a community-based task-shifting psychosocial intervention for individuals with psychosis in Chile: Perspectives from users. Int J Soc Psychiatry. 2019 Feb;65(1):38-45. doi: 10.1177/0020764018815204.
Results Reference
background
PubMed Identifier
24288454
Citation
Baumgartner JN, da Silva TF, Valencia E, Susser E. Measuring social integration in a pilot randomized controlled trial of critical time: intervention-task shifting in Latin America. Cad Saude Colet. 2012 Jan;20(4):10.1590/S1414-462X2012000400005. doi: 10.1590/S1414-462X2012000400005.
Results Reference
background
PubMed Identifier
28596904
Citation
Yang L, Pratt C, Valencia E, Conover S, Fernandez R, Burrone MS, Cavalcanti MT, Lovisi G, Rojas G, Alvarado R, Galea S, Price LN, Susser E. RedeAmericas: building research capacity in young leaders for sustainable growth in community mental health services in Latin America. Glob Ment Health (Camb). 2017 Feb 14;4:e3. doi: 10.1017/gmh.2017.2. eCollection 2017.
Results Reference
background
PubMed Identifier
31066775
Citation
Mascayano F, Alvarado R, Andrews HF, Jorquera MJ, Lovisi GM, Souza FM, Pratt C, Rojas G, Restrepo-Toro ME, Fader K, Gorroochurn P, Galea S, Dahl CM, Cintra J, Conover S, Burrone MS, Baumgartner JN, Rosenheck R, Schilling S, Sarucao KR, Stastny P, Tapia E, Cavalcanti MT, Valencia E, Yang LH, Susser E. Implementing the protocol of a pilot randomized controlled trial for the recovery-oriented intervention to people with psychoses in two Latin American cities. Cad Saude Publica. 2019 May 2;35(4):e00108018. doi: 10.1590/0102-311X00108018.
Results Reference
background
PubMed Identifier
35678081
Citation
Mascayano F, Alvarado R, Andrews HF, Baumgartner JN, Burrone MS, Cintra J, Conover S, Dahl CM, Fader KM, Gorroochurn P, Galea S, Jorquera MJ, Lovisi GM, Mitkiewicz de Souza F, Pratt C, Restrepo-Toro ME, Rojas G, Rodrigues Sarucao K, Rosenheck R, Schilling S, Shriver T, Stastny P, Tapia E, Cavalcanti MT, Valencia E, Yang LH, Restrepo Henao A, Martinez-Ales G, Romero Pardo V, Gomez Alemany T, Susser E. A Recovery-Oriented Intervention for People With Psychosis: A Pilot Randomized Controlled Trial. Psychiatr Serv. 2022 Nov 1;73(11):1225-1231. doi: 10.1176/appi.ps.202000843. Epub 2022 Jun 9.
Results Reference
derived
Links:
URL
http://www.cugmhp.org/research/redeamericas/
Description
RedeAmericas is a National Institute of Mental Health (NIMH)-funded regional network or 'hub' for public mental health research in Latin America.

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Critical Time Intervention-Task Shifting: Randomized Controlled Trial

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