Feasibility and Efficacy of a Digital Mental Health Intervention for Teen Wildfire Survivors
NCT ID: NCT03868761
Last Updated: 2020-11-24
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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COMPLETED
NA
7 participants
INTERVENTIONAL
2019-04-01
2020-11-22
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Single Arm
21 male and female teenage participants will be randomized to one of three varying baseline assessment periods of two, four, or six weeks. Multiple baseline is a type of single-case experimental design (SCED) that is a time- and cost-effective method for evaluating efficacy of a new treatment, Sonoma Rises. The randomization of participants to baseline periods of varying lengths enables assessment of whether symptom changes occur when, and only when, the intervention is applied.
Sonoma Rises
All participants will receive the intervention, Sonoma Rises, a mobile app designed by psychologists at the National Center for PTSD for wildfire survivors to facilitate recovery from disaster. Users can access evidence-informed tools to help cope with stress, heal from loss, prioritize self-care, connect with others, manage anger, and track their mood using validated assessments. There are also tools designed just for teens and users are linked to psychoeducation on disaster and health and other mental health resources and services.
Interventions
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Sonoma Rises
All participants will receive the intervention, Sonoma Rises, a mobile app designed by psychologists at the National Center for PTSD for wildfire survivors to facilitate recovery from disaster. Users can access evidence-informed tools to help cope with stress, heal from loss, prioritize self-care, connect with others, manage anger, and track their mood using validated assessments. There are also tools designed just for teens and users are linked to psychoeducation on disaster and health and other mental health resources and services.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Screen positive for PTSD (Child Trauma Screening Questionnaire = 5 or higher)
3. Have regular access to a smart phone and a computer
4. Have a personal email address
5. Speak and read English fluently
6. Have parental consent
Exclusion Criteria
2. Serious self-reported physical health concerns necessitating surgery or with prognosis \<6 months
3. A positive screen for a current Substance User Disorder (CRAFFT = 2 or higher)
4. Current self-reported suicidal ideation
5. Self-reported pregnancy
6. Self-reported less than four weeks of stable prescription medication for anxiety, anti-depressant, and sleep promoting medications prior to the screening assessment
13 Years
17 Years
ALL
Yes
Sponsors
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Stanford University
OTHER
Responsible Party
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Adrienne Julie Heinz
Research Health Scientist
Principal Investigators
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Adrienne Heinz, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Stanford University
Locations
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Stanford University
Palo Alto, California, United States
Countries
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Other Identifiers
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IRB-49196
Identifier Type: -
Identifier Source: org_study_id