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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04507360
Other study ID # STUDY00010958
Secondary ID 1R01MH125179-01
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 15, 2021
Est. completion date November 30, 2024

Study information

Verified date May 2024
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This proposal is a partnership between Mental Health America (MHA), a nonprofit mental health advocacy and resource organization, Talkspace (TS), a for-profit, online digital psychotherapy organization, and the University of Washington's Schools of Medicine and Computer Science Engineering (UW). The purpose of this partnership is to create a digital mental health research platform leveraging MHA and TS's marketing platforms and consumer base to describe the characteristics of optimal engagement with digital mental health treatment, and to identify effective, personalized methods to enhance motivation to engage in digital mental health treatment in order to improve mental health outcomes. These aims will be met by identifying and following at least 100,000 MHA and TS consumers over the next 4 years, apply machine learning approaches to characterizing client engagement subtypes, and apply micro-randomized trials to study the effectiveness of motivational enhancement strategies and response to digital mental health treatment.


Description:

Digital mental health (DMH) is the use of technology to improve population well-being through rapid disease detection, outcome measurement, and care. Although several randomized clinical trials have demonstrated that digital mental health tools are highly effective, most consumers do not sustain their use of these tools. The field currently lacks an understanding of DMH tool engagement, how engagement is associated with well-being, and what practices are effective at sustaining engagement. In this partnership between Mental Health America (MHA), Talkspace (TS) and the University of Washington (UW), the investigators propose a naturalistic and experimental, theory-driven program of research, with the aim of understanding 1) how consumer engagement in self-help and clinician assisted DMH varies and what engagement patterns exist, 2) the association between patterns of engagement and important consumer outcomes, and 3) the effectiveness of personalized strategies for optimal engagement with DMH treatment. This study will prospectively follow a large, naturalistic sample of MHA and TS consumers, and will apply machine learning, user-centered design strategies, and micro randomized and sequential multiple assignment randomized (SMART) trials to address these aims. As is usual practice for both platforms, consumers will complete online mental health screening and assessment, and the investigators will be able to classify participants by disease status and symptom severity. The sample that the investigators will be working with will not be limited by diagnosis or co-morbidities. Participants will be 10 years old and older and enter the MHA and TS platforms prospectively over 4 years. For aim 1, participant data will be analyzed statistically to reveal differences in engagement and dropout across groups based on demographics, symptoms and platform activity. For aim 2, the investigators will use supervised machine learning techniques to identify subtypes based on consumer demographics, engagement patterns with DMH, reasons for disengagement, success of existing MHA and TS engagement strategies, and satisfaction with the DMH tools, that are predictive of future engagement patterns. Finally, based on the outcomes from aim 2, in aim 3a the investigators will conduct focus groups applying user centered design strategies to identify and co-build potentially effective engagement strategies for particular client subtypes. The investigators will then conduct a series of micro-randomized and SMART trials to determine which theory-driven engagement strategies, co-designed with users, have the greatest fit with subtypes developed under aim 2. The investigators will test the effectiveness of these strategies to 1) prevent disengagement from those who are more likely to have poor outcomes after disengagement, 2) improve movement from motivation to volition and, 3) enhance optimal dose of DMH engagement and consequently improve mental health outcomes. These data will be analyzed using longitudinal mixed effects models with effect coding to estimate the effectiveness of each strategy on client engagement behavior and mental health outcomes. The purpose of aim 3b is to identify effective engagement strategies tailored to client needs and demographics to increase MHA website engagement, and to better understand how self-help mental health resources can help people overcome negative thinking and support healthier thought processes. The investigators will compare effective engagement strategies tailored to subtypes developed under aim 2 to study the mediated impact of engagement strategies on consumer mental health outcomes. The study team will determine if engagement strategies targeted to consumer engagement subtype will enhance engagement and in turn result in improved clinical outcomes. These will be compared to generic strategies that are not subtype targeted. All aim 3b activities will occur with MHA, broken down into two parts: (Study 1) a sequential multiple assignment randomized trial (SMART) and (Study 2) a Do-It-Yourself (DIY) tool longitudinal randomized control trial (RCT). Study 1 will use a SMART to examine methods to optimize engagement with MHA's website, and Study 2 will recruit participants for a longitudinal monthlong study where they are randomly assigned to a control group, the use of a DIY tool without Artificial Intelligence (AI), or the use of a DIY tool with AI to examine the efficacy of using a digital tool to improve mental health functioning. An AI tool that uses machine learning/Natural Language Processing (NLP)/AI methods was developed to personalize and tailor an intervention to improve engagement and completion outcomes. The study focuses on a specific, popular DIY tool that teaches cognitive restructuring. Pilot work showed that (1) engagement and completion rates on DIY tools can be low, and (2) a pilot AI tool had significantly higher engagement and completion rates. These differences may arise due to AI support, User Interface/User Experience/design differences, other factors, or a combination thereof. Additionally, the efficacy of the digital tool to improve mental health functioning is unknown. Study 2 will recruit participants who will be randomly assigned to one of three groups for a longitudinal month-long study: thrice-weekly DIY tool use with AI, without AI, or a control group.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 570
Est. completion date November 30, 2024
Est. primary completion date August 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Phase 3b Study 1 (SMART): Users of MHA website, engaging from Internet Protocol (IP) addresses in the US, who have chosen to start the PHQ-9 depression screener in English. Must be those who can read English. - Phase 3b Study 2 (DIY): PHQ-9 or GAD score of 10 or greater, users of MHA website, 18 years of age or older. Exclusion Criteria: - Phase 3b Study 1 (SMART): None - Phase 3b Study 2 (DIY): Younger than 18 years old, Non-English or Non-Spanish speaking, PHQ-9 less than 10, outside of US, have more than a little familiarity with the concept of cognitive reframing.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Study 1, Generic Response
Participants will be provided with the generic/current response to screening.
Study 1, Tailored Response
Participants will be provided with a response to screening that is tailored to the match between screening score (above or below depression criteria) and expressed need for mental health support (yes or no).
Study 1, Top Resources
Participants will be provided with links to the top list of 4 MHA resources.
Study 1, Tailored Resources by Desired Resources
Participants will be provided with links to MHA resources aligned with their expressed interest (e.g., additional screening, self help tools).
Study 1, Embedded single-question DIY
A single DIY question will be embedded within the content page.
Study 1, Embedded full DIY within content page
The full DIY tool will be embedded within the content page.
Study 1, Single question plus full DIY
A single question plus the full DIY tool will be embedded within the content page.
Study 1, Content-as-usual
The content page will not include any embedded DIY tool.
Study 2, Control
Participants in the DIY control group will receive psychoeducation materials in W0. They will view content as usual (no DIY).
Study 2, DIY tool without AI
Participants in the DIY tool without AI group will be instructed to use the DIY tool 3 times a week.
Study 2, DIY tool with AI
Participants in the DIY tool with AI group will be instructed to use the DIY tool with AI 3 times a week.
Study 1, Tailored Resources by Demographics
Participants will be provided with links to MHA resources tailored to sexuality (Lesbian, Gay, Bisexual, Transgender, or Queer) status and age range.

Locations

Country Name City State
United States Mental Health America Alexandria Virginia
United States Groop Internet Platform DBA Talkspace New York New York
United States University of Washington Seattle Washington

Sponsors (4)

Lead Sponsor Collaborator
University of Washington Mental Health America, National Institute of Mental Health (NIMH), Talkspace

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Study 1: Mental Health America Engagement Time spent on webpages after screening results provided Through active web session, an average of 10 minutes
Primary Study 1: Mental Health America Engagement Number of article(s) read after screening results provided Through active web session, an average of 10 minutes
Primary Study 1: Mental Health America Disengagement Proportion of users leaving website after shown assigned intervention Through active web session, an average of 10 minutes
Primary Study 1: DIY Completion Rate Percent of completion of the DIY tool Week 1, Week 2, Week 3, Week 4
Primary Study 2: Engagement (Dosage) Number of times using the DIY tool Week 1, Week 2, Week 3, Week 4
Primary Study 2: Tool Use Helpfulness Measured using one item (Using the tool has been helpful to me in dealing with my negative thoughts and emotions) on a scale of 1 (strongly agree) to 4 (strongly disagree). Note: includes 5 qualitative questions, not included here. Week 1, Week 2, Week 3, Week 4, Week 8
Primary Study 2: Emotion Mechanisms Emotion mechanisms are measured using a 16-item scale for the control group and a 17-item scale for the DIY, no AI and DIY, with AI groups on a scale of 1-10, with higher scores meaning more intensity for each specific emotion. At W8, Emotion Mechanisms are measured using 22 items on a scale of 1-10. Scores will be assessed using mean item-level scores. Participants are asked about their emotions (e.g., confidence, anxiety, comfort, hopefulness, motivation) about their ability to address negative thoughts. These include, for example, identifying thinking traps, reframing negative thoughts, commitment to regularly engaging in the reframing practice, and motivation to keep improving their reframing skills. For the four items that ask about feeling anxious or intimidated, higher scores indicate greater anxiety and intimidation. For the remaining items, higher scores indicate better emotion mechanisms. Week 1, Week 2, Week 3, Week 4, Week 8
Primary Study 2: Tool Mechanisms Tool Mechanisms is measured using 4 items about reframing. The items measure relatability/believability, helpfulness, memorability, and learnability on a scale of 1( strongly agree) to 4 (Strongly disagree). Scores will be assessed using mean item-level scores, with higher scores indicating better outcomes after using a DIY tool. Week 1, Week 2, Week 3, Week 4
Primary Study 2: Tool Mechanisms (Part 2) Tool Mechanisms (Part 2) is measured using 2 items about belief change and emotion change on a scale of 1 to 10. Scores will be assessed using mean item-level scores, with higher scores indicating stronger beliefs and emotions after completing a DIY tool. Note: this also includes 1 qualitative question; not included here. Week 1, Week 2, Week 3, Week 4
Primary Study 2: Hopefulness Hopefulness is measured using a single item (How hopeful do you feel about the future?) on a scale of 1 to 10. Week 1, Week 2, Week 3, Week 4, Week 8
Primary Study 2: DIY Skill Use: Competencies of Cognitive Therapy Scale - Self-Report The Competencies of Cognitive Therapy Scale will be used to ask participants about how much they have used specific strategies to cope with negative moods, primarily negative automatic thoughts, in the last 4 weeks. The current study will use items 20, 28, 21, 6, 24, and 11; all items are rated on a scale of 1 (not at all) to 7 (completely). Higher scores indicate better outcomes. Scores will be assessed using mean item-level scores. These items ask participants about the following strategies: re-evaluating the situation, taking time to step back from a situation and considering that their negative thoughts might be inaccurate, actively working to develop more rational views, having a specific action plan of things they could do to cope, taking time to consider other factors that may have been involved, and taking note of what they were thinking and working to develop a more balanced view. Note: this also includes 3 qualitative questions; not included here. Week 1, Week 2, Week 3, Week 4, Week 8
Secondary Study 2: Patient Health Questionnaire (PHQ-9) The Patient Health Questionnaire (PHQ-9) consists of 9 depression items. Each item is associated with a Diagnostic and Statistical Manual (DSM) symptom of depression. Participants rate whether or not they have experienced the symptom over the last two weeks, with severity ratings of 0 to 3. Total scores range from 0 to 27, with higher scores indicating greater severity of depression symptoms. It is one of the few measures that is brief (it takes less than one minute to give) and has been found to have excellent sensitivity to change over time. Used for screening and will be used as a moderator. Baseline, Week 1, Week 2, Week 3, Week 4, Week 8
Secondary Study 2: Generalized Anxiety Disorder (GAD-7) A 7- item screener for generalized anxiety. It consists of items related to Generalized Anxiety Disorder (GAD). Participants rate how much anxiety they have experienced in the last two weeks on a scale of 0 to 3. Total scores range from 0 to 21, with higher scores indicating greater severity of anxiety symptoms. The scale is a valid screener for GAD. Used for screening and will be used as a moderator. Baseline, Week 1, Week 2, Week 3, Week 4, Week 8
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