- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04806321
Project SOLVE: Trial of a Brief Digital Problem-solving Intervention
Project SOLVE: A School-based Trial of a Universal Single-session Digital Problem-solving Intervention for Adolescent Mental Health
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
More than 20% of adolescents will experience at least one mental health disorder or problem before adulthood that warrants treatment, yet 80% of these adolescents will never receive care. This need-to-access gap appears to be heightened during the current coronavirus disease pandemic and its resulting disruptions to healthcare and education systems. Both within and beyond the context of the pandemic, preventive mental health interventions are positioned to help adolescents build and strengthen coping strategies that can preclude the emergence of mental health difficulties that require more resource-intensive levels of clinical care. Preventive mental health interventions delivered via digital platforms and within school-based settings might be especially scalable.
The current school-based trial is designed to test one such strategy that harnesses technology to boost the scalability of adolescent mental health interventions: a brief (one 30 minute session) digital program designed to empower adolescents (10-14 years old) to solve, rather than be overwhelmed by, everyday problems (Project SOLVE). Single-session interventions designed to help adolescents cultivate adaptive mindsets have reduced anxiety and depression among adolescents with and without elevated symptoms of these disorders. Building on this strong foundation, Project SOLVE targets these mental health challenges with problem solving skills-one of the most versatile, commonly used, and potent therapeutic techniques for adolescents.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Massachusetts
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Cambridge, Massachusetts, United States, 02138
- Harvard University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adolescent is in grades 6-8 (inclusive) at partnering schools
- Adolescent is between the ages of 10-14 years (inclusive) at the time of study enrollment
- Adolescent and at least one guardian consent to adolescent participation in study
- Adolescent reads English well enough to effectively complete the digital programs
- Adolescent has access to a digital device
Exclusion Criteria:
- Adolescent is non-English speaking, as the programs are only available in English
- Adolescent does not have access to a digital device
- Adolescent has an intellectual disability that precludes comprehension of the program content
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: TRIPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Project SOLVE
This program is self-guided, digital, and approximately 30 minutes in length.
Content is designed to help adolescents solve, rather than be overwhelmed by, everyday problems.
The program includes: (1) An introduction to problem solving; (2) Testimonials from "valued others" (older adolescents; celebrities) describing their use of problem solving skills; (3) Evidence from studies that our brains are capable of problem solving and that problem solving can be helpful; and (4) Activities designed to enable adolescents to practice sequential problem solving using a few steps (SOLVE Steps).
|
This 30-minute, self-guided, digital program is designed to help adolescents solve, rather than be overwhelmed by, everyday problems.
|
|
ACTIVE_COMPARATOR: Project SUCCESS
This program is self-guided, digital, and approximately 30 minutes in length.
Content is designed to help adolescents improve their study skills.
This program includes: (1) An introduction to study skills; (2) Testimonials from "valued others" describing their use of study skills; (3) Description of helpful and commonly used study skills (e.g., note-taking); and (4) Activities designed to encourage adolescents to practice these skills in their daily lives.
|
This 30-minute, self-guided, digital program is designed to help adolescents develop study skills.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Behavior and Feelings Survey (Internalizing Subscale) From Baseline to 3-month Follow-Up
Time Frame: Baseline to 3-month follow-up
|
Trajectories of self-reported symptoms of anxiety and depression from the 6-item (each item rated on a 0-4 scale, with higher ratings indicating more symptoms) Internalizing subscale of the Behavior and Feelings Survey.
Total scores range from 0 to 24, with higher scores indicating more symptoms.
|
Baseline to 3-month follow-up
|
|
Change in Behavior and Feelings Survey (Internalizing Subscale) From Baseline to 12-month Follow-Up
Time Frame: Baseline to 12-month follow-up
|
Trajectories of self-reported symptoms of anxiety and depression from the 6-item (each item rated on a 0-4 scale, with higher ratings indicating more symptoms) Internalizing subscale of the Behavior and Feelings Survey.
Total scores range from 0 to 24, with higher scores indicating more symptoms.
|
Baseline to 12-month follow-up
|
|
Change in State Hope Scale Pathways Subscale From Immediately Pre-Intervention to Immediately Post-Intervention
Time Frame: Immediately pre-intervention to immediately post-intervention
|
Change in self-reported hopefulness, as measured via the 3-item "pathways" (planning of ways to meet goals) subscale of the State Hope Scale.
Each item is rated on a 1-8 scale and total scores range from 1 to 24, with higher scores indicating higher levels of hopefulness.
|
Immediately pre-intervention to immediately post-intervention
|
|
Change in Beck Hopelessness Scale From Immediately Pre-Intervention to Immediately Post-Intervention
Time Frame: Immediately pre-intervention to immediately post-intervention
|
The Beck Hopelessness Scale (BHS) asks adolescents to rate 4 statements based on their sense of hopelessness.
Participants rate the 4 statements on a 4 point scale ranging from 0 (Absolutely Disagree) to 3 (Absolutely Agree).
Total score ranges from 0 to 12, with higher scores indicating greater levels of hopelessness.
|
Immediately pre-intervention to immediately post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Program Acceptability and Helpfulness
Time Frame: Immediately post-intervention
|
Post-intervention feedback on the program's perceived acceptability and helpfulness as measured via a 7-item scale, with each item rated on a 1-5 scale, with higher scores indicating greater acceptability and helpfulness.
|
Immediately post-intervention
|
|
Change in Behavior and Feelings Survey (Externalizing Subscale) From Baseline to 3-month Follow-Up
Time Frame: Baseline to 3-month follow-up
|
Trajectories of self-reported misbehavior from the 6-item (each item rated on a 0-4 scale, with higher ratings indicating more symptoms) Externalizing subscale of the Behavior and Feelings Survey.
Total scores range from 0 to 24, with higher scores indicating more symptoms.
|
Baseline to 3-month follow-up
|
|
Change in Behavior and Feelings Survey (Externalizing Subscale) From Baseline to 12-month Follow-Up
Time Frame: Baseline to 12-month follow-up
|
Trajectories of self-reported misbehavior from the 6-item (each item rated on a 0-4 scale, with higher ratings indicating more symptoms) Externalizing subscale of the Behavior and Feelings Survey.
Total scores range from 0 to 24, with higher scores indicating more symptoms.
|
Baseline to 12-month follow-up
|
|
Change in State Hope Scale From Baseline to 3-Month Follow-Up
Time Frame: Baseline to 3-month follow-up
|
Change in self-reported total hopefulness from the 6-item (each item rated on a 1-8 scale, with higher scores indicating greater hopefulness) State Hope Scale, as well as self-reported scores on the 3-item "agency" (goal-directed determination) and 3-item "pathways" (planning of ways to meet goals) subscales of this measure.
|
Baseline to 3-month follow-up
|
|
Change in State Hope Scale From Baseline to 12-Month Follow-Up
Time Frame: Baseline to 12-month follow-up
|
Change in self-reported total hopefulness from the 6-item (each item rated on a 1-8 scale, with higher scores indicating greater hopefulness) State Hope Scale, as well as self-reported scores on the 3-item "agency" (goal-directed determination) and 3-item "pathways" (planning of ways to meet goals) subscales of this measure.
|
Baseline to 12-month follow-up
|
|
Change in Beck Hopelessness Scale From Baseline to 3-Month Follow-Up
Time Frame: Baseline to 3-month follow-up
|
The Beck Hopelessness Scale (BHS) asks adolescents to rate 4 statements based on their sense of hopelessness.
Participants rate the 4 statements on a 4 point scale ranging from 0 (Absolutely Disagree) to 3 (Absolutely Agree).
Total score ranges from 0 to 12, with higher scores indicating greater levels of hopelessness.
|
Baseline to 3-month follow-up
|
|
Change in Beck Hopelessness Scale From Baseline to 12-Month Follow-Up
Time Frame: Baseline to 12-month follow-up
|
The Beck Hopelessness Scale (BHS) asks adolescents to rate 4 statements based on their sense of hopelessness.
Participants rate the 4 statements on a 4 point scale ranging from 0 (Absolutely Disagree) to 3 (Absolutely Agree).
Total score ranges from 0 to 12, with higher scores indicating greater levels of hopelessness.
|
Baseline to 12-month follow-up
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
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
- IRB20-1791
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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