Depressive SymptomsNCT06138730
Evaluating a Virtual Mentoring Program Plus Mental Health Videos for Teens
A study testing Appa Complete and Appa Lite in people with Depressive Symptoms and Anxiety Disorders and Symptoms, run by Appa Health at 1 site in United States.
Trial summary
This clinical trial evaluates Appa Health, a mental health smartphone and computer app for teenagers. Appa is built from two components. Component #1 shares short TikTok-style videos with teens to cover techniques from a science-backed mental health treatment, Cognitive Behavioral Therapy. Read more about this study
- Who is it for?
- Ages 13 to 18 yearsHealthy volunteers can take part
- Conditions the study is for
- Depressive Symptoms, Anxiety Disorders and Symptoms
- What is being tested?
- Appa Complete and Appa Lite
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 475 participants
- Where
- 1 siteUnited States
- Study dates
- 12 Feb 2024to 1 Nov 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 13 to 18 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- 13 to 18 years old
- Generalized Anxiety Disorder screen or Patient Health Questionnaire screen scores of 10 or higher
- Living in the United States
- Speak English
- Read/comprehend English at a 5th grade level or higher (treatment delivery is in English)
- Able to appropriately and independently engage with study intervention (i.e., without parental support)
Show all 9Show fewer
- Must be a caregiver (e.g., parent, grandparent, custodian) of a youth participant in the study
- Must be a mentor with a youth mentee in the study
- Must supervise a mentor with a mentee in the study
Who cannot join
- Psychotic disorders
- Substance use disorders
- Active engagement in self-harm
- Active suicidal ideation (intent or plan)
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Digital Delivery of Evidence-Based Mental Health Content and Mentoring to Adolescents
This clinical trial evaluates Appa Health, a mental health smartphone and computer app for teenagers. Appa is built from two components. Component #1 shares short TikTok-style videos with teens to cover techniques from a science-backed mental health treatment, Cognitive Behavioral Therapy. These videos are designed by mental health experts and delivered by mental health influencers. Component #2 pairs teens with peer mentors with similar life experiences, who help guide teens through each week's video content. All peer mentors are trained and supervised by licensed mental health experts. The researchers believe Appa Health improves teens' mental health and well-being through teens' strengthened relationships and support from their mentor, as well as through the skills they gain through watching the videos. This study hopes to understand: (1) whether these Appa Health components improve teens' mental health and well-being, (2) how these components might improve teen outcomes, and (3) costs associated with each of these components. To answer these questions, the researchers will compare two versions of Appa support: Appa Complete and Appa Lite. Appa Complete involves pairing teens with mentors and sharing videos. Appa Lite involves only sharing videos with teens. First, the researchers will conduct a small version of this study to test procedures. Seventy-five teenagers (13-18 years old) with high depression or anxiety scores will be randomly given either: Appa Complete (mentoring + videos), Appa Lite (videos only), or a Waiting List Control. Based on the results of this smaller study, the researchers will change study procedures to improve teens' experiences and engagement in this research. After completing this smaller study, the researchers will run a larger version of the same study with 400 more teens. After teens are randomly given Appa Complete, Appa Lite, or a Waiting List Control, the researchers will test whether Appa's two treatment components improve teens' depression, anxiety, well-being, and other related outcomes. The researchers expect both Appa Complete and Appa Lite will improve teens' outcomes more than the Waiting List Control. The researchers also expect Appa Complete will improve teens' outcomes more than Appa Lite. The researchers will also measure costs associated with giving teens both treatment components and use this information to improve Appa's services for future teens.
Read the detailed description
Pilot Study (1 year). Optimize Study Procedures and Participant Retention (6 months). In an initial pilot study with N=75 youth, the researchers will examine the adapted Appa Health and research study content, offering data for optimization and retention incentive decisions prior to larger scale RCT through the following research questions (RQs): RQ 1.1: Are research and incentive protocols sufficient for recruiting and retaining adolescents in the study, and how can they be optimized? RQ 1.2. Do Appa's modified engagement strategies developed in preliminary studies increase use of CBT video content? This pilot study will enable the research team to identify and address any problems in recruitment, study procedures, and retention prior to the effectiveness trial.
Setting. The study will be carried out within the Appa Health remote platform, which comprises over 20 trained youth mentors serving, on average, 400 youth every 3 months. Clients come primarily from school-based partnerships. Appa has several existing school partners who refer students to Appa either through a paid partnership from the school or through access to parents of students.
Recruitment and Randomization. Participants will be recruited from the Appa Health client population using email outreach. As described in the Commercialization Plan, the Appa client base from individual paying clients, school systems, and B2B customers is expected to be sufficient to meet this goal within the study timeframe. Screening of youth using the PHQ-8 and GAD is standard protocol for Appa; those who score above 10 on either instrument will be invited to participate in the study. Due to the relatively small sample size of the pilot trial, the research team will use stratified random sampling to ensure approximate balance to the three study conditions on baseline covariates (gender, age, baseline severity on GAD \& PHQ-8, race/ethnicity, and LGBTQ status), with stratification blocks created via nearest neighbor matching on all variables.
Interventions. Youth will be randomized to three conditions, which in the larger RCT will enable analyses of the main effect of the traditional Appa package as compared to a waiting list control group, as well as exploring the impact of a light touch version of Appa for commercial purposes. This will also permit examination of the impact of the two components on specific psychosocial mechanisms, as appropriate in an experimental therapeutics paradigm.
"Appa Lite": Unguided EBP videos and materials. Participants assigned to the Appa Lite condition will have unlimited access to the Appa website, including short form CBT-based videos and materials such as an emotions wheel pdf and thoughts, feelings, and behavior worksheets.
"Appa Complete": Weekly mentorship meetings \& guided CBT videos. Participants assigned to Appa Complete will have unlimited access to the Appa website and materials described in Appa Lite, along with weekly mentorship meetings with a trained and supervised near-peer mentor with whom they have been matched.
"Waiting List Control": Participants assigned to the waitlist control will receive a small pdf packet of psychoeducational materials and will be permitted to use Appa at the end of the 12 weeks of data collection. Families assigned to this condition will not pay for Appa's services while on the waitlist.
Data Collection. The REDCap electronic data collection application will be used to collect data from mentors, supervisors, and caregivers at enrollment (baseline) and at midpoint (6 weeks) and end (12 weeks).REDCap will also be used to collect survey data from adolescents at enrollment (baseline) and at midpoint (6 weeks) and end (12 weeks). Adolescent data collection will include quantitative and qualitative surveys and assessments focused on therapeutic interactions (mentorship fidelity, frequency of video watching and mentor interactions, supportive accountability), mechanisms of change (e.g., use of CBT, confidence in relationships, reduced isolation), clinical outcomes (depression, anxiety, top problems, quality of life/flourishing, self-esteem), possible moderators (demographics, alliance, mentor-adolescent match), and study-related measures (research burden, open-ended comments). To control for compensatory mental health service use by participants in any condition, the prohibition of which in the study would be unethical, the research team will collect data on non-Appa services received elsewhere, including mentorship. Adolescents will be incentivized with $25 per survey timepoint and non-monetary, low burden incentives such as humorous messaging and GIFs. Mentor data collection will focus on mentor fidelity to the supportive accountability model (coded audio recordings of mentor sessions and text communication), moderators (surveys of alliance, mentor-client match), and time diaries for the cost analysis. Mentor supervisors will also provide time diary data. Caregivers will provide data on caregiver strain and the financial burden of adolescent care due to mental health, and caregivers will be incentivized with $5 per administration. Fidelity to mentorship will be measured by coding three randomly selected audio recordings of mentorship sessions and 10 randomly selected text exchanges for each client. Cost assessments. Activity-based costing will estimate the incremental cost of Appa Complete and Appa Lite. The research team will estimate the direct cost of video production and mentoring including web hosting, payments to video creators, mentor salary, training, and supervision. Data collection using time diaries will occur via online surveys of mentors and supervisors. The research team will identify activities related to mentoring and associated labor and non-labor inputs such as time, supplies, travel, overhead, and costs associated with meetings. Activities will be categorized to facilitate understanding of cost allocation. The price of goods and services will be available via budget and expense reports.
Effectiveness Trial: Study Appa Costs and Effectiveness (2.5 years). A large randomized controlled trial with N=400 youth will replicate the pilot study, excluding measures collected on research burden and incentive satisfaction. If the research team does not make substantive changes to the product after the initial pilot trial, the main effectiveness trial analysis will include all 75 pilot participants (total N=up to 475 youth). The three-arm design will enable Appa to determine the cost and effectiveness of each Appa component and enable evidence-based decision making on the commercial viability of scaling these components. Appa will learn the degree to which users engage in components, the cost of those components, and the impact of those components on important mechanisms and outcomes. The research team will test the following hypotheses: H1a-j: At 12 week follow-up, teens in the Appa Complete condition will have significantly greater improvement than both other conditions on primary outcomes of a) youth top problem severity, b) use of CBT skills, c) self-efficacy for CBT; as well as secondary outcomes of youth d) depression, e) anxiety, f) quality of life, g) self-esteem, h) existential isolation, and caregiver i) strain, and h) financial burden. H2a-h: Clients in the Appa Lite condition will have superior outcomes than the control group on a) use of CBT skills, b) depression, c) anxiety, d) top problem severity, e) quality of life, f) self-esteem, g) caregiver strain and h) caregiver financial burden; H3a-d: Near peer mentoring will increase engagement in digital tools and mechanisms such that those who receive mentoring (Appa Complete), when compared to Appa Lite, will a) watch more videos, b) have greater efficacy for CBT skills, c) report greater use of CBT skills, and d) report greater meaning and purpose. Exploratory research questions: ERQ1: Do hypothesized mechanisms (meaning and purpose, identification with mentor, self-efficacy for using CBT, fidelity to practice and supportive accountability, and use of CBT skills) mediate the impact of Appa on depression, anxiety, and top problem severity? ERQ2: Is the impact of Appa on top problem severity, depression, and anxiety moderated by client demographics, mentor alliance, frequency of meetings, degree of demographic match between client and mentor, or dosage of video use? The research team is particularly interested in whether there are differential outcomes by race and social identity.
Cost-effectiveness. H4: Appa Complete will be more expensive but more cost-effective than Appa Lite.
Participants. Inclusion and exclusion criteria will replicate the pilot study.
Recruitment. Recruitment methods will replicate the pilot study. The research team will recruit approximately 400 adolescents, roughly 133 in each condition. The research team assumes 20% attrition for a final complete sample of 320; however, these analytic methods permit inclusion of all available data including dropouts. If the research team does not make substantive changes to the product after the initial pilot trial, the main effectiveness trial analysis will include all 75 pilot participants (total N=up to 475 youth).
Randomization. Random assignment to condition will occur using urn randomization at the client level to ensure roughly equal numbers in each condition based on key hypothesized moderators including gender, age, baseline severity on GAD \& PHQ-8, race/ethnicity, and LGBTQ status. Urn randomization is an adaptive biased-coin method that ensures balance on multiple covariates in rolling-enrollment designs but approaches complete randomization in larger sample sizes.
Data collection. Data collection will replicate the pilot study.
- Being tested
- Appa Complete, Appa Lite
- Keywords
- Depression, Anxiety, Adolescence, Digital Mental Health, Mentorship
- Medical subject headings
- Depression, Anxiety Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Appa CompleteBehavioural
Weekly mentorship meetings \& guided CBT videos. Participants assigned to Appa Complete will have unlimited access to the Appa website and materials described in Appa Lite, along with weekly mentorship meetings with a trained and supervised near-peer mentor with whom they have been matched. Matching is based on preference for mentor gender, racial/ethnic minority status, and LGBTQ status and is designed to increase the sense of identification with the mentor and peer-mentor alliance. Virtual meetings begin with a review and discussion of the video and other materials for the week. Mentors ask about how clients are incorporating their CBT learnings into their life, share ways they have used the focal skills in their own lives, illustrate skills use in popular culture, and provide problem solving strategies. Each week has a specific prompt to ensure that clients are applying the concepts and skills they are learning and can talk about any questions or reflections with their mentors.
Appa LiteBehavioural
Unguided EBP videos and materials. Participants assigned to the Appa Lite condition will have unlimited access to the Appa website, including short form CBT-based videos and materials such as an emotions wheel pdf and thoughts, feelings, and behavior worksheets. The website is structured so that the materials are presented in a developmentally appropriate manner consistent with evidence-based principles in a 12-week format, beginning with general psychoeducation to define mental health, proceeding to introducing CBT and basic CBT skills such as identifying thoughts, feelings, and behaviors, layering on applying specific CBT skills, and ending with reflective journal exercises. Client progress through the materials will be completely unguided.
| Study group | Role | What they receive |
|---|---|---|
| Appa Complete | Experimental | Participants in this arm will be granted access to Appa Complete (i.e., weekly mentorship + CBT videos). Receives: Behavioral: Appa Complete |
| Appa Lite | Active comparator | Participants in this arm will be granted access to Appa Lite (i.e., CBT videos without weekly mentorship). Receives: Behavioral: Appa Lite |
| Waiting List Control | No intervention | Participants in this arm will be given a mental health resources packet. In 12 weeks (after the study period), they will be granted access to Appa Lite. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Youth-Reported Psychosocial Functioning
Youth TOP Problems Scale
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Use of CBT
Skills of Cognitive Therapy Measure (SCT)
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Self-Efficacy for CBT
Self-Efficacy for CBT Scale
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Secondary outcomes (8)
Youth-Reported Depressive Symptoms
Patient Health Questionnaire (PHQ-8)
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Anxiety Symptoms
Generalized Anxiety Disorder (GAD-7)
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Quality of Life and Flourishing
Mental Health Continuum-Short Form (MHC-SF)
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Self-Esteem
Adolescent Self-Esteem Questionnaire
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Existential Isolation
Existential Isolation Scale
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Caregiver-Reported Youth Psychosocial Functioning
Caregiver Youth TOP Problems Scale
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Caregiver-Reported Strain
Caregiver Strain Questionnaire
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Caregiver-Reported Financial Burden
Caregiver Financial Burden Items
Measured: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Nov 2023
- Study start12 Feb 2024
- Primary completion1 Nov 2026 (estimated)
- Study completion1 Nov 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Depressive SymptomsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 475 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Appa Health
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Johns Hopkins University
- Responsible party
- Sponsor
- Investigators
- Michelle Kaufman, PhD, Principal investigator, Johns Hopkins UniversityRobert Miller, JD, Principal investigator, Appa Health
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06138730
- Sponsor's protocol ID
- STUDY00017822
- Status last verified
- Jun 2025
- First submitted
- 14 Nov 2023
- Last updated
- 20 Jun 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Jun 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Digital Delivery of Evidence-Based Mental Health Content and Mentoring to Adolescents
- ClinicalTrials.gov ID
- NCT06138730
- Acronym / sponsor ID
- STUDY00017822
- Keywords
- Depression, Anxiety, Adolescence, Digital Mental Health, Mentorship
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 475 participants (estimated)
- Lead sponsor
- Appa HealthIndustry (pharma, biotech, devices)
- Collaborators
- Johns Hopkins University
- Study start
- 12 Feb 2024 (actual)
- Primary completion
- 1 Nov 2026 (estimated)
- Study completion
- 1 Nov 2026 (estimated)
- First posted
- 18 Nov 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This clinical trial evaluates Appa Health, a mental health smartphone and computer app for teenagers. Appa is built from two components. Component #1 shares short TikTok-style videos with teens to cover techniques from a science-backed mental health treatment, Cognitive Behavioral Therapy. These videos are designed by mental health experts and delivered by mental health influencers. Component #2 pairs teens with peer mentors with similar life experiences, who help guide teens through each week's video content. All peer mentors are trained and supervised by licensed mental health experts. The researchers believe Appa Health improves teens' mental health and well-being through teens' strengthened relationships and support from their mentor, as well as through the skills they gain through watching the videos. This study hopes to understand: (1) whether these Appa Health components improve teens' mental health and well-being, (2) how these components might improve teen outcomes, and (3) costs associated with each of these components. To answer these questions, the researchers will compare two versions of Appa support: Appa Complete and Appa Lite. Appa Complete involves pairing teens with mentors and sharing videos. Appa Lite involves only sharing videos with teens. First, the researchers will conduct a small version of this study to test procedures. Seventy-five teenagers (13-18 years old) with high depression or anxiety scores will be randomly given either: Appa Complete (mentoring + videos), Appa Lite (videos only), or a Waiting List Control. Based on the results of this smaller study, the researchers will change study procedures to improve teens' experiences and engagement in this research. After completing this smaller study, the researchers will run a larger version of the same study with 400 more teens. After teens are randomly given Appa Complete, Appa Lite, or a Waiting List Control, the researchers will test whether Appa's two treatment components improve teens' depression, anxiety, well-being, and other related outcomes. The researchers expect both Appa Complete and Appa Lite will improve teens' outcomes more than the Waiting List Control. The researchers also expect Appa Complete will improve teens' outcomes more than Appa Lite. The researchers will also measure costs associated with giving teens both treatment components and use this information to improve Appa's services for future teens.
Detailed description
Pilot Study (1 year). Optimize Study Procedures and Participant Retention (6 months). In an initial pilot study with N=75 youth, the researchers will examine the adapted Appa Health and research study content, offering data for optimization and retention incentive decisions prior to larger scale RCT through the following research questions (RQs): RQ 1.1: Are research and incentive protocols sufficient for recruiting and retaining adolescents in the study, and how can they be optimized? RQ 1.2. Do Appa's modified engagement strategies developed in preliminary studies increase use of CBT video content? This pilot study will enable the research team to identify and address any problems in recruitment, study procedures, and retention prior to the effectiveness trial.
Setting. The study will be carried out within the Appa Health remote platform, which comprises over 20 trained youth mentors serving, on average, 400 youth every 3 months. Clients come primarily from school-based partnerships. Appa has several existing school partners who refer students to Appa either through a paid partnership from the school or through access to parents of students.
Recruitment and Randomization. Participants will be recruited from the Appa Health client population using email outreach. As described in the Commercialization Plan, the Appa client base from individual paying clients, school systems, and B2B customers is expected to be sufficient to meet this goal within the study timeframe. Screening of youth using the PHQ-8 and GAD is standard protocol for Appa; those who score above 10 on either instrument will be invited to participate in the study. Due to the relatively small sample size of the pilot trial, the research team will use stratified random sampling to ensure approximate balance to the three study conditions on baseline covariates (gender, age, baseline severity on GAD \& PHQ-8, race/ethnicity, and LGBTQ status), with stratification blocks created via nearest neighbor matching on all variables.
Interventions. Youth will be randomized to three conditions, which in the larger RCT will enable analyses of the main effect of the traditional Appa package as compared to a waiting list control group, as well as exploring the impact of a light touch version of Appa for commercial purposes. This will also permit examination of the impact of the two components on specific psychosocial mechanisms, as appropriate in an experimental therapeutics paradigm.
"Appa Lite": Unguided EBP videos and materials. Participants assigned to the Appa Lite condition will have unlimited access to the Appa website, including short form CBT-based videos and materials such as an emotions wheel pdf and thoughts, feelings, and behavior worksheets.
"Appa Complete": Weekly mentorship meetings \& guided CBT videos. Participants assigned to Appa Complete will have unlimited access to the Appa website and materials described in Appa Lite, along with weekly mentorship meetings with a trained and supervised near-peer mentor with whom they have been matched.
"Waiting List Control": Participants assigned to the waitlist control will receive a small pdf packet of psychoeducational materials and will be permitted to use Appa at the end of the 12 weeks of data collection. Families assigned to this condition will not pay for Appa's services while on the waitlist.
Data Collection. The REDCap electronic data collection application will be used to collect data from mentors, supervisors, and caregivers at enrollment (baseline) and at midpoint (6 weeks) and end (12 weeks).REDCap will also be used to collect survey data from adolescents at enrollment (baseline) and at midpoint (6 weeks) and end (12 weeks). Adolescent data collection will include quantitative and qualitative surveys and assessments focused on therapeutic interactions (mentorship fidelity, frequency of video watching and mentor interactions, supportive accountability), mechanisms of change (e.g., use of CBT, confidence in relationships, reduced isolation), clinical outcomes (depression, anxiety, top problems, quality of life/flourishing, self-esteem), possible moderators (demographics, alliance, mentor-adolescent match), and study-related measures (research burden, open-ended comments). To control for compensatory mental health service use by participants in any condition, the prohibition of which in the study would be unethical, the research team will collect data on non-Appa services received elsewhere, including mentorship. Adolescents will be incentivized with $25 per survey timepoint and non-monetary, low burden incentives such as humorous messaging and GIFs. Mentor data collection will focus on mentor fidelity to the supportive accountability model (coded audio recordings of mentor sessions and text communication), moderators (surveys of alliance, mentor-client match), and time diaries for the cost analysis. Mentor supervisors will also provide time diary data. Caregivers will provide data on caregiver strain and the financial burden of adolescent care due to mental health, and caregivers will be incentivized with $5 per administration. Fidelity to mentorship will be measured by coding three randomly selected audio recordings of mentorship sessions and 10 randomly selected text exchanges for each client. Cost assessments. Activity-based costing will estimate the incremental cost of Appa Complete and Appa Lite. The research team will estimate the direct cost of video production and mentoring including web hosting, payments to video creators, mentor salary, training, and supervision. Data collection using time diaries will occur via online surveys of mentors and supervisors. The research team will identify activities related to mentoring and associated labor and non-labor inputs such as time, supplies, travel, overhead, and costs associated with meetings. Activities will be categorized to facilitate understanding of cost allocation. The price of goods and services will be available via budget and expense reports.
Effectiveness Trial: Study Appa Costs and Effectiveness (2.5 years). A large randomized controlled trial with N=400 youth will replicate the pilot study, excluding measures collected on research burden and incentive satisfaction. If the research team does not make substantive changes to the product after the initial pilot trial, the main effectiveness trial analysis will include all 75 pilot participants (total N=up to 475 youth). The three-arm design will enable Appa to determine the cost and effectiveness of each Appa component and enable evidence-based decision making on the commercial viability of scaling these components. Appa will learn the degree to which users engage in components, the cost of those components, and the impact of those components on important mechanisms and outcomes. The research team will test the following hypotheses: H1a-j: At 12 week follow-up, teens in the Appa Complete condition will have significantly greater improvement than both other conditions on primary outcomes of a) youth top problem severity, b) use of CBT skills, c) self-efficacy for CBT; as well as secondary outcomes of youth d) depression, e) anxiety, f) quality of life, g) self-esteem, h) existential isolation, and caregiver i) strain, and h) financial burden. H2a-h: Clients in the Appa Lite condition will have superior outcomes than the control group on a) use of CBT skills, b) depression, c) anxiety, d) top problem severity, e) quality of life, f) self-esteem, g) caregiver strain and h) caregiver financial burden; H3a-d: Near peer mentoring will increase engagement in digital tools and mechanisms such that those who receive mentoring (Appa Complete), when compared to Appa Lite, will a) watch more videos, b) have greater efficacy for CBT skills, c) report greater use of CBT skills, and d) report greater meaning and purpose. Exploratory research questions: ERQ1: Do hypothesized mechanisms (meaning and purpose, identification with mentor, self-efficacy for using CBT, fidelity to practice and supportive accountability, and use of CBT skills) mediate the impact of Appa on depression, anxiety, and top problem severity? ERQ2: Is the impact of Appa on top problem severity, depression, and anxiety moderated by client demographics, mentor alliance, frequency of meetings, degree of demographic match between client and mentor, or dosage of video use? The research team is particularly interested in whether there are differential outcomes by race and social identity.
Cost-effectiveness. H4: Appa Complete will be more expensive but more cost-effective than Appa Lite.
Participants. Inclusion and exclusion criteria will replicate the pilot study.
Recruitment. Recruitment methods will replicate the pilot study. The research team will recruit approximately 400 adolescents, roughly 133 in each condition. The research team assumes 20% attrition for a final complete sample of 320; however, these analytic methods permit inclusion of all available data including dropouts. If the research team does not make substantive changes to the product after the initial pilot trial, the main effectiveness trial analysis will include all 75 pilot participants (total N=up to 475 youth).
Randomization. Random assignment to condition will occur using urn randomization at the client level to ensure roughly equal numbers in each condition based on key hypothesized moderators including gender, age, baseline severity on GAD \& PHQ-8, race/ethnicity, and LGBTQ status. Urn randomization is an adaptive biased-coin method that ensures balance on multiple covariates in rolling-enrollment designs but approaches complete randomization in larger sample sizes.
Data collection. Data collection will replicate the pilot study.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Appa Complete | Experimental | Behavioral: Appa CompleteParticipants in this arm will be granted access to Appa Complete (i.e., weekly mentorship + CBT videos). |
| Appa Lite | Active comparator | Behavioral: Appa LiteParticipants in this arm will be granted access to Appa Lite (i.e., CBT videos without weekly mentorship). |
| Waiting List Control | No intervention | –Participants in this arm will be given a mental health resources packet. In 12 weeks (after the study period), they will be granted access to Appa Lite. |
Who may qualify
- Ages
- 13 to 18 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (9 listed)
- 13 to 18 years old
- Generalized Anxiety Disorder screen or Patient Health Questionnaire screen scores of 10 or higher
- Living in the United States
- Speak English
- Read/comprehend English at a 5th grade level or higher (treatment delivery is in English)
Key exclusion criteria (4 listed)
- Psychotic disorders
- Substance use disorders
- Active engagement in self-harm
- Active suicidal ideation (intent or plan)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Appa CompleteWeekly mentorship meetings \& guided CBT videos. Participants assigned to Appa Complete will have unlimited access to the Appa website and materials described in Appa Lite, along with weekly mentorship meetings with a trained and supervised near-peer mentor with whom they have been matched. Matching is based on preference for mentor gender, racial/ethnic minority status, and LGBTQ status and is designed to increase the sense of identification with the mentor and peer-mentor alliance. Virtual meetings begin with a review and discussion of the video and other materials for the week. Mentors ask about how clients are incorporating their CBT learnings into their life, share ways they have used the focal skills in their own lives, illustrate skills use in popular culture, and provide problem solving strategies. Each week has a specific prompt to ensure that clients are applying the concepts and skills they are learning and can talk about any questions or reflections with their mentors. | Behavioural | Appa Complete |
| Appa LiteUnguided EBP videos and materials. Participants assigned to the Appa Lite condition will have unlimited access to the Appa website, including short form CBT-based videos and materials such as an emotions wheel pdf and thoughts, feelings, and behavior worksheets. The website is structured so that the materials are presented in a developmentally appropriate manner consistent with evidence-based principles in a 12-week format, beginning with general psychoeducation to define mental health, proceeding to introducing CBT and basic CBT skills such as identifying thoughts, feelings, and behaviors, layering on applying specific CBT skills, and ending with reflective journal exercises. Client progress through the materials will be completely unguided. | Behavioural | Appa Lite |
Primary outcome
Youth-Reported Psychosocial Functioning
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth TOP Problems Scale
Youth-Reported Use of CBT
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Skills of Cognitive Therapy Measure (SCT)
Youth-Reported Self-Efficacy for CBT
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Self-Efficacy for CBT Scale
8 secondary outcomes
Youth-Reported Depressive Symptoms
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Anxiety Symptoms
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Quality of Life and Flourishing
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Self-Esteem
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Youth-Reported Existential Isolation
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Caregiver-Reported Youth Psychosocial Functioning
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Caregiver-Reported Strain
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Caregiver-Reported Financial Burden
Time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Jun 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Michelle Kaufman, PhD principal investigator
Johns Hopkins University
Robert Miller, JD principal investigator
Appa Health
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Appa Complete and Appa Lite in people with Depressive Symptoms and Anxiety Disorders and Symptoms, run by Appa Health at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 20 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Youth-Reported Psychosocial Functioning (time frame: Baseline (T1) + 6 Weeks Survey (T2) + 12 Weeks Survey (T3)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jun 2025; AzTrials last refreshed its copy on 29 Oct 2026.