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Internet-delivered Cognitive Behavioral Treatment of Depression and Anxiety in Latin American College Students

Primary Purpose

Major Depressive Disorder, Generalized Anxiety Disorder

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Yo Puedo Sentirme Bien- Clinician-Guided version
Yo Puedo Sentirme Bien- Self-Guided version
Sponsored by
Instituto Nacional de Psiquiatría Dr. Ramón de la Fuente
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder focused on measuring iCBT, Latin America, College Students, Depression, Anxiety

Eligibility Criteria

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

Inclusion Criteria:

At least 18 years of age, screens positive for major depressive disorder and/or generalized anxiety disorder, student enrolled in one of the participating universities

Exclusion Criteria:

Screens positive for bipolar disorder, screens positive for psychosis, active suicidality

Sites / Locations

  • Universidad Nacional de ColombiaRecruiting
  • Universidad Cooperativa de ColombiaRecruiting
  • Fundación Universitaria del Area AndinaRecruiting
  • Universidad Popular de CesarRecruiting
  • Universidad Autonoma MetropolitanaRecruiting
  • Universidad Autonoma de Baja CaliforniaRecruiting
  • Universidad la SalleRecruiting
  • Universidad Nacional Autonoma de MéxicoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Clinician-Guided iCBT

Self-guided iCBT

Arm Description

Both help-seeking students recruited from university clinics and non-help-seeking students recruited from needs assessment survey and outreach will receive internet delivered cognitive behavioral therapy guided by clinicians

Help-seeking students recruited from university clinics will receive self-guided internet delivered cognitive behavioral therapy while on waitlist. Non-help seeking students recruited from needs assessment survey and outreach will receive the self-guided version of internet delivered cognitive behavioral therapy.

Outcomes

Primary Outcome Measures

Patient Health Questionnaire-9 (PHQ-9)
Self-report measure of depressive symptoms in the prior 2 weeks. Scores range from 0 to 27 with higher scores representing greater depressive symptomatology.
Generalized Anxiety Disorder-7 (GAD-7)
Self-report measure of anxiety symptoms in the prior 2 weeks. Scores range from 0 to 21 with higher scores representing greater anxiety.
Patient Health Questionnaire-9 (PHQ-9)
Self-report measure of depressive symptoms in the prior 2 weeks. Scores range from 0 to 27 with higher scores representing greater depressive symptomatology.
Generalized Anxiety Disorder-7 (GAD-7)
Self-report measure of anxiety symptoms in the prior 2 weeks. Scores range from 0 to 21 with higher scores representing greater anxiety.

Secondary Outcome Measures

Sheehan Disability Scale (SDS)
Self-report measure of impairment due to mental health in four life areas in the prior 2 weeks. Scores in each area range from 0 to 10 with higher scores reflecting greater impairment.
Sheehan Disability Scale (SDS)
Self-report measure of impairment due to mental health in four life areas in the prior 2 weeks. Scores in each area range from 0 to 10 with higher scores reflecting greater impairment.

Full Information

First Posted
February 28, 2021
Last Updated
June 2, 2023
Sponsor
Instituto Nacional de Psiquiatría Dr. Ramón de la Fuente
Collaborators
National Institute of Mental Health (NIMH), Harvard Medical School (HMS and HSDM)
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1. Study Identification

Unique Protocol Identification Number
NCT04780542
Brief Title
Internet-delivered Cognitive Behavioral Treatment of Depression and Anxiety in Latin American College Students
Official Title
Computerized Detection and Internet-based Treatment of Common Mental Disorders Among College Students in Two Latin American LMICs
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
May 2025 (Anticipated)
Study Completion Date
June 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Nacional de Psiquiatría Dr. Ramón de la Fuente
Collaborators
National Institute of Mental Health (NIMH), Harvard Medical School (HMS and HSDM)

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 aim is to evaluate short term and longer term treatment effects of internet-delivered cognitive behavioral therapy compared to treatment as usual for college students with anxiety and/or depression in low-middle income countries of Latin America.
Detailed Description
This study is designed to detect, engage, and experimentally evaluate the effects of internet-based cognitive behavior therapy (e-CBT) to treat college students in two Latin American low-middle income countries (LMICs; Colombia and Mexico) with major depressive disorder and/or generalized anxiety disorder, with or without other comorbid common mental disorders (CMDs). Detection and engagement will be based on inexpensive internet-based recruitment and administration of self-report surveys. The intervention will be based on inexpensive e-CBT to address the low resources in LMICs. The study builds on prior research by collaborators in the WHO World Mental Health (WMH) survey consortium and WMH International College Study (WMH-ICS) initiative documenting high prevalence, impairment, and unmet need for treatment of CMDs among college students around the world and significant effects of e-CBT in treating these disorders in high income countries. First, the investigators will carry out a pragmatic clinical trial with students seeking treatment for CMDs at student clinics in universities in Colombia and Mexico. Students on waitlists for student clinic services will be offered a possibility of receiving guided or self-guided e-CBT immediately while staying on the list. 33% of the students with CMD who express interest will be randomized to guided e-CBT, another 33% to self-guided e-CBT, and the remaining 33% to treatment as usual (TAU), where the latter is defined as remaining on the waiting list. Short-term aggregate intervention effects will be assessed 90 days after randomization and longer-term effects 12 months after randomization. The investigators will then use ensemble machine learning methods to predict heterogeneity of treatment effects of e-CBT versus TAU and develop a precision treatment rule (PTR) to predict which students will respond best to which intervention. A SMART design will then be implemented in which 50% of a second cohort of students from the same sample frame (i.e., students seeking treatment for CMDs at student clinics in the participating universities) will be randomized to the treatment arm predicted to be optimal by the PTR and the other 50% to randomization across arms. Based on the findings from the first pragmatic trial, none of the students were optimized by TAU. Therefore for the next cohort of students they will be randomized only to two arms, guided and unguided. Additionally, the investigators will use outreach to recruit students into the trial who might not otherwise seek treatment from student clinics. Two procedures will be used here. In the first, students will be recruited from annual WMH-ICS internet-based mental health needs assessment surveys that will be carried out with a probability sample of students to estimate unmet need for treatment and barriers to treatment. Students who respond to these surveys and meet inclusion criteria and are not in treatment will be randomized to guided e-CBT, self-guided e-CBT, and treatment as usual (only in first pragmatic trial) in student clinics to determine if access to guided and self-guided e-CBT reduces the unmet need for treatment among students with CMDs who fail to seek treatment at student health clinics. The second will expand recruitment by sending emails to random subsamples of students notifying them of the availability of the internet-based interventions and inviting them to participate in a trial. Students that respond to this announcement will then be recruited and randomized into the same three arms as among students that participated in the annual WMH-ICS survey.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder, Generalized Anxiety Disorder
Keywords
iCBT, Latin America, College Students, Depression, Anxiety

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
Participant recruiters will be blinded to the participant's intended treatment arm.
Allocation
Randomized
Enrollment
1500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Clinician-Guided iCBT
Arm Type
Experimental
Arm Description
Both help-seeking students recruited from university clinics and non-help-seeking students recruited from needs assessment survey and outreach will receive internet delivered cognitive behavioral therapy guided by clinicians
Arm Title
Self-guided iCBT
Arm Type
Active Comparator
Arm Description
Help-seeking students recruited from university clinics will receive self-guided internet delivered cognitive behavioral therapy while on waitlist. Non-help seeking students recruited from needs assessment survey and outreach will receive the self-guided version of internet delivered cognitive behavioral therapy.
Intervention Type
Behavioral
Intervention Name(s)
Yo Puedo Sentirme Bien- Clinician-Guided version
Intervention Description
Internet delivered Cognitive Behavioral Therapy- Guided version
Intervention Type
Behavioral
Intervention Name(s)
Yo Puedo Sentirme Bien- Self-Guided version
Intervention Description
Internet delivered Cognitive Behavioral Therapy- Self-Guided version
Primary Outcome Measure Information:
Title
Patient Health Questionnaire-9 (PHQ-9)
Description
Self-report measure of depressive symptoms in the prior 2 weeks. Scores range from 0 to 27 with higher scores representing greater depressive symptomatology.
Time Frame
90 days
Title
Generalized Anxiety Disorder-7 (GAD-7)
Description
Self-report measure of anxiety symptoms in the prior 2 weeks. Scores range from 0 to 21 with higher scores representing greater anxiety.
Time Frame
90 days
Title
Patient Health Questionnaire-9 (PHQ-9)
Description
Self-report measure of depressive symptoms in the prior 2 weeks. Scores range from 0 to 27 with higher scores representing greater depressive symptomatology.
Time Frame
12 months
Title
Generalized Anxiety Disorder-7 (GAD-7)
Description
Self-report measure of anxiety symptoms in the prior 2 weeks. Scores range from 0 to 21 with higher scores representing greater anxiety.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Sheehan Disability Scale (SDS)
Description
Self-report measure of impairment due to mental health in four life areas in the prior 2 weeks. Scores in each area range from 0 to 10 with higher scores reflecting greater impairment.
Time Frame
90 days
Title
Sheehan Disability Scale (SDS)
Description
Self-report measure of impairment due to mental health in four life areas in the prior 2 weeks. Scores in each area range from 0 to 10 with higher scores reflecting greater impairment.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least 18 years of age, screens positive for major depressive disorder and/or generalized anxiety disorder, student enrolled in one of the participating universities Exclusion Criteria: Screens positive for bipolar disorder, screens positive for psychosis, active suicidality
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Corina Benjet, PhD
Phone
+525541605332
Email
cbenjet@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Corina Benjet, PhD
Organizational Affiliation
Instituto Nacional de Psiquiatría
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universidad Nacional de Colombia
City
Bogotá
Country
Colombia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jose Ignacio Ruiz Perez, PhD
Facility Name
Universidad Cooperativa de Colombia
City
Medellín
Country
Colombia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nayib Ester Carrasco Tapias, PhD
Email
nayib.carrasco@ucc.edu.co
Facility Name
Fundación Universitaria del Area Andina
City
Valledupar
Country
Colombia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lorena Cudris Torres, PhD
Facility Name
Universidad Popular de Cesar
City
Valledupar
Country
Colombia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Libia Alvis, PhD
Facility Name
Universidad Autonoma Metropolitana
City
Ciudad de Mexico
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carlos Contreras, PhD
Facility Name
Universidad Autonoma de Baja California
City
Ensenada
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eunice Vargas-Contreras, PhD
Email
eunice.vargas@uabc.edu.mx
Facility Name
Universidad la Salle
City
León
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Abigail Paz Pérez
Facility Name
Universidad Nacional Autonoma de México
City
Mexico City
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Benjamin Guerrero Lopez, MD
Email
jefaturadpsm.unam@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
First, we will document and make available all imputations, weights, and constructed variables used in our analyses. Second, we will host a project webinars to present an overview of the data and answer questions. The webinars will be widely advertised in list serves, including any such sites recommended by NIMH, as well as to NIH training programs. An English version of the webinars will be hosted by the US collaborators. A Spanish version will be hosted by the Mexican collaborators. Third, we will set up and man a project Q&A web site in which public users can ask questions and get answers about issues involved in working with the data. Again, the site will be both in English and Spanish. Fourth, we will gather up written versions of all questions asked by public users along with our written response (including any documentation or computer files sent along with these answers) and post these on the website in both English and Spanish as reference documents for future public users.
IPD Sharing Time Frame
Data will become available in Year 5, once trials are concluded
IPD Sharing Access Criteria
By written request
Citations:
PubMed Identifier
35658942
Citation
Benjet C, Kessler RC, Kazdin AE, Cuijpers P, Albor Y, Carrasco Tapias N, Contreras-Ibanez CC, Duran Gonzalez MS, Gildea SM, Gonzalez N, Guerrero Lopez JB, Luedtke A, Medina-Mora ME, Palacios J, Richards D, Salamanca-Sanabria A, Sampson NA. Study protocol for pragmatic trials of Internet-delivered guided and unguided cognitive behavior therapy for treating depression and anxiety in university students of two Latin American countries: the Yo Puedo Sentirme Bien study. Trials. 2022 Jun 2;23(1):450. doi: 10.1186/s13063-022-06255-3.
Results Reference
derived

Learn more about this trial

Internet-delivered Cognitive Behavioral Treatment of Depression and Anxiety in Latin American College Students

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