EMA Baseline Screening System for Therapists Who Treat Youths With Depressive Symptoms
NCT ID: NCT04830527
Last Updated: 2022-05-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
60 participants
INTERVENTIONAL
2020-11-24
2021-11-30
Brief Summary
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The hypotheses for this trial are:
1. Applying an EMA baseline screening application one week before the beginning of treatment for youth depression will significantly improve the TA.
2. Applying an EMA baseline screening application one week before the beginning of treatment for youth depression will significantly improve initial adherence.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SCREENING
DOUBLE
Study Groups
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Intervention group
Patients in experimental group will receive EMA prompts. Therapists in this group will receive a summarized PDF report before the beginning of the first psychotherapy session. The report will include graphic summarized data from the EMA prompts.
EMA prompting for patients
EMA prompting will consist of the delivery of the PHQ-4 and PANAS questionnaires, as well as basic identification, therapy motivations and expectations, location, current activity and social interactions.
These prompts will be presented to patients during a 7 day period, 5 times per day.
PDF Reports for therapists
After the patients' EMA data is collected, a previously designed R script will summarize and transform the data into a brief and graphic report for therapists in the experimental arm of the study. These reports are intended to provide detailed information about the patients' mood, anxiety levels, positive and negative affects, as well as crossed data such as mood according to location, anxiety according to activity, etc.
Control group
Patients in control group will receive the EMA prompts in the same manner as patients in the experimental group.
Therapists in this group will not receive the PDF reports, and instead will get raw scores from a screening evaluation conducted with patients in the recruitment phase of the study.
EMA prompting for patients
EMA prompting will consist of the delivery of the PHQ-4 and PANAS questionnaires, as well as basic identification, therapy motivations and expectations, location, current activity and social interactions.
These prompts will be presented to patients during a 7 day period, 5 times per day.
Interventions
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EMA prompting for patients
EMA prompting will consist of the delivery of the PHQ-4 and PANAS questionnaires, as well as basic identification, therapy motivations and expectations, location, current activity and social interactions.
These prompts will be presented to patients during a 7 day period, 5 times per day.
PDF Reports for therapists
After the patients' EMA data is collected, a previously designed R script will summarize and transform the data into a brief and graphic report for therapists in the experimental arm of the study. These reports are intended to provide detailed information about the patients' mood, anxiety levels, positive and negative affects, as well as crossed data such as mood according to location, anxiety according to activity, etc.
Eligibility Criteria
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Inclusion Criteria
* Scoring from eleven to nineteen points in the PHQ-9 questionnaire.
* Having completed the eighth grade of basic education.
\- Having 1 or more years of clinical experience.
Exclusion Criteria
* Having a depressive episode as part of a bipolar disorder diagnosis
* Having suicidal thoughts and/or behaviour as measured by the PHQ-9 and evaluated by the physician.
* Alcohol and/or substance abuse.
* Having less than 1 year of clinical experience.
* Having participated in the design of PDF reports.
18 Years
24 Years
ALL
No
Sponsors
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ANID - Millennium Science Initiative Program - NCS17_03 Millennium Nucleus to Improve the Mental Health of Adolescents and Youths (Imhay), Santiago, Chile
UNKNOWN
Millennium Institute on Immunology and Immunotherapy
OTHER
Center for Psychotherapy Research, University Hospital Heidelberg, Heidelberg, Germany
UNKNOWN
Vania Martínez-Nahuel
OTHER
Responsible Party
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Vania Martínez-Nahuel
Dr.
Locations
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CEMERA, Faculty of Medicine, Universidad de Chile
Santiago, Santiago Metropolitan, Chile
Countries
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References
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Other Identifiers
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030-2020
Identifier Type: -
Identifier Source: org_study_id
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