- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02038855
International Latino Research Partnership (ILRP)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Our study aims to conduct behavioral health services research focused on rapid screening and referral; as well as testing the feasibility, acceptability and efficacy of integrated behavioral health services in primary care clinics for migrant Latinos with co-occurring substance use and mental health problems, and increased risk of HIV.
A key activity for the first phase, the screening project, is administering a screener to at least 450 Latino migrant patients across the 3 sites (n=150 each in Boston, Madrid, and Barcelona) from primary care and behavioral health (substance abuse and mental health) services. We intend to test the referral process for screened participants in need of treatment to identify barriers and streamline the process. We will analyze data to optimize the screening battery and protocol to use in Phase 2, the IIDEA intervention.
In Phase 2, we intend to enroll, randomize and collect data on 360 total patients across the 3 sites - 180 in the intervention condition and 180 in the control condition (120 in each site, 60 in the intervention condition and 60 in the control condition). The 10 session IIDEA intervention will be offered to Latino patients by trained clinicians with at least a Masters level of training. The intervention is designed to help patients to address and prevent mental health and substance use problems and will be culturally adapted to Latino populations in Boston, Madrid and Barcelona. Usual care - the control group - receives treatment as usual, for patients in primary care identified with a mental health or substance use problem. 5 Research interviews will be conducted to assess outcomes, for patients in both the intervention and usual care arms.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Madrid, Spain
- Universidad Autonoma de Madrid Medical School
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Catalonia
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Barcelona, Catalonia, Spain
- Vall d'Hebron University Hospital
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Massachusetts
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Somerville, Massachusetts, United States, 02143
- Cambridge Health Alliance
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Latino migrants
- Must speak English or Spanish
- 18-70 years of age
- Screen positive to at least one substance use and one mental health problem
Exclusion Criteria:
- Current or recent (last 3 months) substance use treatment (more than 1 visit with a provider at a behavioral health clinic)
- Planning to receive behavioral health services (i.e., have an appointment scheduled in the next 2 months)
- Evidence that the patient lacks capacity to consent to the study
- Evidence of current suicidal risk or harm to others (affirmative responses to questions 4 and/or 5 on Paykel suicide questionnaire)- patient can be rescreened in 30 days
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: IIDEA
Patients in the Integrated Intervention for Dual Problems and Early Action (IIDEA) arm will receive the 10 session intervention administered in person and via telephone.
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Integrated Intervention for Dual Problems and Early Action (IIDEA) includes psycho-education, Cognitive Behavioral Therapy and mindfulness; identifies triggers and challenging thoughts; provides motivational techniques for reducing substance use and/or smoking cravings; incorporates cognitive restructuring to identify and correct negative thinking patterns influenced by depression, anxiety and/or trauma; and includes self-monitoring of thoughts and risk behaviors that contribute to substance use, smoking and increased HIV risk.
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No Intervention: Usual Care
Patients in this arm receive usual care for dual-diagnosis symptoms of mental health and substance use.
They receive 5 check-in calls from a care manager to assess safety.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Addiction Severity Index (ASI) - Alcohol (change)
Time Frame: Baseline, 2 months, 4 months, 6 months, 12 months
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The ASI is a semi-structured interview designed to address seven potential problem areas in substance-abusing patients; this outcome measure refers to the Alcohol problem area.
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Baseline, 2 months, 4 months, 6 months, 12 months
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Addiction Severity Index (ASI) - Drugs (change)
Time Frame: Baseline, 2 months, 4 months, 6 months, 12 months
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The ASI is a semi-structured interview designed to address seven potential problem areas in substance-abusing patients; this outcome measure refers to the Drug problem area.
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Baseline, 2 months, 4 months, 6 months, 12 months
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Change on Urine Drug Test (change)
Time Frame: Baseline, 2 months, 4 months, 6 months, 12 months
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Technical analysis of a biological specimen (urine) to determine the presence or absence of specified parent drugs or their metabolites.
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Baseline, 2 months, 4 months, 6 months, 12 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Generalized Anxiety Disorder 7-item (GAD-7) Scale (change)
Time Frame: Baseline, 2 months, 4 months, 6 months, 12 months
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The GAD-7 is a questionnaire for screening and severity measuring of generalized anxiety disorder (GAD).
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Baseline, 2 months, 4 months, 6 months, 12 months
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PTSD Checklist for DSM-V (PCL-5)
Time Frame: Baseline, 2 months, 4 months, 6 months, 12 months
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The PCL-5 is is a 20-item self-report measure that assesses the 20 DSM-5 symptoms of PTSD.
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Baseline, 2 months, 4 months, 6 months, 12 months
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Patient Health Questionnaire (PHQ-9) (change)
Time Frame: Baseline, 2 months, 4 months, 6 months, 12 months
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The PHQ-9 is a 9-item screening questionnaire to determine level of depressive disorder.
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Baseline, 2 months, 4 months, 6 months, 12 months
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Hopkins Symptom Checklist-20
Time Frame: Baseline, 2 months, 4 months, 6 months, 12 months
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The HSCL-20 is a symptom inventory for depression that indicates severity of psychological distress.
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Baseline, 2 months, 4 months, 6 months, 12 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Margarita Alegria, Ph.D., CMMHR, Cambridge Health Alliance and Harvard Medical School
- Principal Investigator: Enrique Baca-Garcia, Ph.D., Universidad Autonoma de Madrid
- Principal Investigator: Francisco Collazos, MD, Vall d'Hebron University Hospital
Publications and helpful links
General Publications
- Levison JH, Alegria M, Wang Y, Markle SL, Fuentes L, Mejia DL, Tarbox A, Albarracin Garcia L, Cellerino L, El-Bassel N. High HIV/STI Test Acceptance Through a Behavioral Health Encounter in Latino Immigrants with Substance Use and Mental Health Problems. AIDS Behav. 2019 Apr;23(4):835-846. doi: 10.1007/s10461-019-02413-y.
- Alegria M, Falgas-Bague I, Collazos F, Carmona Camacho R, Lapatin Markle S, Wang Y, Baca-Garcia E, Le Cook B, Chavez LM, Fortuna L, Herrera L, Qureshi A, Ramos Z, Gonzalez C, Aroca P, Albarracin Garcia L, Cellerino L, Villar A, Ali N, Mueser KT, Shrout PE. Evaluation of the Integrated Intervention for Dual Problems and Early Action Among Latino Immigrants With Co-occurring Mental Health and Substance Misuse Symptoms: A Randomized Clinical Trial. JAMA Netw Open. 2019 Jan 4;2(1):e186927. doi: 10.1001/jamanetworkopen.2018.6927.
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHA-IRB-0910/06/12
- R01DA034952-01A1 (U.S. NIH Grant/Contract)
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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