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NCT Number: NCT07051330

The Advancing Dynamic And Personalized Training Study

This study aims to enhance the Healthy Minds Program (HMP) app by developing and testing a personalized, data-driven approach to optimize long-term well-being. 1100 participants will be enrolled and on study for up to 4 months (4 week intervention plus 3 month follow-up).

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Center for Healthy Minds

Madison, Wisconsin, 53703, United States

Location status: Recruiting

Location contact

Wendy Lau

CONTACT

[email protected]

6088903073

About this study

Participants will be randomly assigned to various training conditions that vary across six factors. Each of the six factors is binary ("yes" vs. "no"), and for each factor there is a 50 percent probability of assignment to either level.

  • Introduction video for the app (yes / no)
  • Introduction video for the training modules (yes / no)
  • Module order based on ACIP score (highest-first / lowest-first)
  • Practice-nudging text messages (yes / no)
  • Microsupport messages during the intervention period (yes / no)
  • Microsupport messages during the follow-up period (yes / no)

Participants will take surveys at baseline, weekly through the 4-week intervention, and 3-month follow-up.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Elevated symptoms of depression (PHQ-9 greater than or equal to 5)
  • proficiency in English
  • access to a smartphone and internet
  • ability to receive text messages

Exclusion criteria

  • Prior experience with meditation
  • Prior use of the Healthy Minds Program app
  • History of psychosis or mania
  • Plans to travel in the next six weeks
  • Suicidal ideation or thoughts of self-harm indicated by PHQ-9 item 9 and BDI item 9
  • Failure to select the correct code word mentioned in the welcome video
  • Not a US citizen
  • Non-permanent resident
  • Self-identification as artificial intelligence (AI)
  • Has a hearing impairment

Treatment and study plan

Healthy Minds Program (HMP) app

Other

All participants will complete baseline surveys, weekly questionnaires (for 4 weeks) through the HMP app intervention, and will be surveyed again at 3-months post-intervention. Participants are randomized to each of the following binary conditions.

  • Introduction video for the app (yes / no)
  • Introduction video for the training modules (yes / no)
  • Module order based on ACIP score (highest-first / lowest-first)
  • Practice-nudging text messages (yes / no)
  • Microsupport messages during the intervention period (yes / no)
  • Microsupport messages during the follow-up period (yes / no

Other names: HMP app

Primary outcomes

  1. Change in PHQ-9

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    PHQ-9 is a 9 item questionnaire where participants report how often in the past 2 weeks they were bothered by specific problems. It is scored on a 4-point Likert scale, where 0=not at all and 4=nearly every day. Scores range from 0-36, where higher scores indicate more depressive symptoms.

Secondary outcomes

  1. Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Depression

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    A computer-adaptive measure of feelings of depression scored from 1 to 5 where higher numbers indicate increased feelings of depression. It provides t-scores with a mean of 50 and SD of 10.

  2. Change in PROMIS Anxiety Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The PROMIS Anxiety Score is a computer adaptive measure of feelings of anxiety in the past 7 days. This is a computer-adaptive survey scored on a 5-point Likert scale from 1 (never) to 5 (always) with higher scores indicating increased anxiety. It provides t-scores with a mean of 50 and SD of 10. Higher t-scores indicate higher levels of anxiety.

  3. Acceptability of Intervention Measure

    Time frame: week 4 (of intervention period)

    The Acceptability of Intervention Measure is a 4-item self-report measure scored on a 5-point Likert scale. Scores range from 1 (completely disagree) to 5 (completely agree), with higher scores indicating more acceptability of the intervention.

  4. Change in Growth Mindset Scale for Well-Being

    Time frame: Baseline, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    A measure of fixed versus incremental mindset regarding well-being. The average across items for a possible range in scores from 1-6 will be measured, with higher scores indicating greater levels of incremental views on well-being (i.e., it can be learned).

  5. HMP engagement measure

    Time frame: Week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    HMP engagement is a 16-item measure which assess participant's usage experience with the Healthy Minds Program. It is scored on a 5-point Likert scale where 1 = Strongly disagree to 5 = Strongly agree. The total possible range of scores is 0-80 where higher scores indicate more positive engagement with the app.

  6. Change in Cannabis Use Disorder Identification Test - Revised (CUDIT-R)

    Time frame: Baseline, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    CUDIT-R is an 8-item survey asking about the participant's relationship to cannabis. It is scored using various scales depending on the item. Scores range from 0 to 32, with higher scores indicating greater risk for cannabis use disorder.

  7. Change in Alcohol Use Disorders Identification Test (AUDIT)

    Time frame: Baseline, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    AUDIT is a 10-item survey asking about the participant's relationship to alcohol. It is scored using various scales depending on the item. Scores range from 0 to 40, with higher scores indicating greater risk for alcohol use disorder.

  8. Change in Healthy Minds Index (HMI) Score

    Time frame: Baseline, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    HMI is a 17-item survey scored on a 5-point Likert scale from 0 (never, none, not at all) to 4 (always, every time, to the highest degree) that assesses awareness, connection, insight, and purpose. Higher scores indicate higher sense of awareness, connection, insight, and purpose. Mean score for each subscale will be reported.

  9. Change in PROMIS Global Health Score

    Time frame: Baseline, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    Global Health is a participant-reported outcome measure that assesses an individual's overall physical and mental health, including their perceptions of general health. It comprises 10 items, with four items assessing Global Physical Health and four assessing Global Mental Health, all based on five core PROMIS domains: physical function, pain, fatigue, emotional distress, and social health. The scores, ranging from 0 to 20, represent the individual's perception of their health, with lower scores indicating greater impairment.

  10. Change in Ruminative Response Scale (RSS) Score

    Time frame: Baseline, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The RRS is a 10-item, 4-point measure of rumination. Each item indicates the frequency of each event by rating a four-point Likert scale ranging from 1 (Almost never) to 4 (Almost always). The total score ranges from 10-40, with higher scores indicating increased tendency to ruminate.

  11. Change in Big Five Inventory-2 Extra Short Form (BFI-2-XS)

    Time frame: Baseline, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    BFI-2-XS is a 15-item questionnaire designed to assess the Big Five personality domains: Extraversion; Agreeableness; Conscientiousness; Negative Emotionality; and, Open-Mindedness. Each trait is assessed with three items, and the total score for each trait ranges from 3 to 15, with higher scores indicating a stronger tendency towards that trait.

  12. Change in Mindfulness Adherence Questionnaire (MAQ)

    Time frame: Week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    MAQ is a 12-item self-report scale designed to assess both the quantity and quality of mindfulness-based practice (MBP), including formal and informal practices. Two items assess the duration of formal practice. The remaining ten items use a 7-point Likert scale ranging from 0 (Never) to 6 (Always) to measure these aspects of mindfulness practice. Scores range from 0-60. Higher scores on the MAQ generally indicate higher levels of practice and/or better quality of practice.

  13. Change in Self-Compassion Scale - Short Form (SCS-SF)

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    SCS-SF is a 12-item survey asking how the participant relates to themself. It is scored on a 5-point Likert scale, where 1 = Almost never and 5 = Almost always. Scores range from 12-60, with higher scores indicating greater self-compassion.

  14. Change in Flourishing Index Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The Flourishing Index is a 10-item questionnaire where participants report their general level of flourishing (e.g., well-being, health, etc.). It is scored on a 0 to 10-point scale, with anchors varying across items. The total score ranges from 0 to 100 with higher scores indicating higher flourishing.

  15. Change in Digital Working Alliance Inventory (DWAI)

    Time frame: week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    DWAI is a six-item questionnaire designed to assess the therapeutic alliance within the Healthy Minds Program (HMP) app. It measures the user's connection and agreement with the app, focusing on the bond, tasks, and goals of the therapeutic relationship. It is scored on a 7-point Likert scale, with scores ranging from 6-42. Higher scores indicate a stronger working alliance with the HMP app.

  16. Change PROMIS Sleep Disturbance Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The PROMIS Sleep Disturbance Score is a measure of sleep in the past 7 days. This is a computer-adaptive survey scored on a 5-point Likert scale with higher scores indicating increased sleep disturbance. It provides t-scores with a mean of 50 and SD of 10. Higher t scores indicate higher levels of sleep disturbances.

  17. Change in PROMIS Meaning and Purpose Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The PROMIS Meaning and Purpose is a computer-adaptive measures which assesses one's sense of life having purpose and that there are good reasons for living. It is scored on a 5-point Likert scale where 1 = strongly disagree to 5 = strongly agree. Higher scores indicate hopefulness, optimism, goal-directedness, and feelings that one's life is worthy. It provides t-scores with a mean of 50 and a standard deviation of 10 in the general population.

  18. Change in Decentering Subscale of Experiencing Questionnaire score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The Decentering subscale of the Experience Questionnaire is an 11-item questionnaire where participants report on their ability to decenter from their experience. It is scored on a 5-point Likert scale where 1 = never to 5 = all the time. The total possible range of scores is 11-55 where higher scores indicate a greater ability to decenter from experience.

  19. Change in NIH Toolbox Loneliness Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The NIH Toolbox Loneliness is a 5-item questionnaire where participants report how often in the past week they have felt loneliness. It is scored on a 5-point Likert scale where 1 = never to 5 = always. The total possible range of scores is 5-25 where higher scores indicate a greater sense of loneliness.

  20. Change in Five-facet Mindfulness Questionnaire: Awareness Subscale (FFMQ-Acting with Awareness) Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The FFMQ-Acting with Awareness subscale is an 8-item survey scored on a 5-point Likert scale from 'never, or very rarely true' to 'very often or always true', for a total possible range of scores from 8-40 where higher scores indicate greater mindfulness awareness.

  21. Change in Five-facet Mindfulness Questionnaire: Non-reactivity Subscale (FFMQ-Non-reactivity) Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The FFMQ- Non-reactivity subscale is a 7-item survey scored on a 5-point Likert scale from 1 = 'never, or very rarely true' to 5 = 'very often or always true', for a total possible range of scores from 7-35 where higher scores indicate greater ability to actively detach from negative thoughts and emotions.

  22. Change in Perceived Stress Scale (PSS) Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    PSS is a 10-item survey scored on a 5-point Likert scale from 0 = never to 4 = very often, for a total possible range of scores from 0-40 where higher scores indicate higher perceived stress.

  23. Morning Daily Diary Items

    Time frame: Daily through the Intervention Period (up to 4 weeks)

    Morning daily diary will include single-item measures of mindfulness, decentering, connection, purpose, depression, anxiety, happiness, energy, stress, busyness, rumination (2 items), sleep quality, motivation to practice meditation, and expectations and challenges related to using the HMP. Each item will be rated on a 5-point Likert scale (1 = not at all, 5 = very much). Higher scores indicate greater levels of the respective construct, such as higher mindfulness, greater decentering, stronger sense of purpose, greater happiness, more severe depression or anxiety, better sleep quality, or greater motivation and perceived helpfulness or frustration with HMP use that morning.

  24. Evening Daily Diary Items

    Time frame: Daily through the Intervention Period (up to 4 weeks)

    Evening daily diary will include single-item measures of mindfulness, decentering, connection, purpose, depression, anxiety, happiness, energy, happy event, stress exposure, rumination (2 items), and expectations related to using the HMP. Each item will be rated on a 5-point Likert scale (1 = not at all, 5 = very much). Higher scores indicate greater levels of the respective construct, such as higher mindfulness, greater decentering, stronger sense of purpose, more severe depression or anxiety, happy event and stressor exposure experience, or greater motivation and perceived helpfulness with HMP use that day.

  25. Percentage of participants with a formal practice

    Time frame: Daily through the Intervention Period (up to 4 weeks)

    Participants' engagement in formal mindfulness practice will be assessed twice a day with a binary yes/no response.

  26. Percentage of participants with a informal practice

    Time frame: Daily through the Intervention Period (up to 4 weeks)

    Participants' engagement in informal mindfulness practice will be assessed twice a day with a 5-point Likert scale (1 = not at all, 5 = all day long).

  27. Percentage of participants received a text message

    Time frame: Daily through the Intervention Period (up to 4 weeks)

    Participants will indicate whether they received a text message from the study that day (yes/no). If they respond "yes," they will then report whether the message encouraged them to apply a wellbeing strategy (yes/no) and rate the extent to which they applied the strategy in their day-to-day activities on a 5-point Likert scale (1 = not at all, 5 = very much).

Other outcomes

  1. Change in Beck Depression Inventory Item 9 Score

    Time frame: Baseline, week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    Item 9 on the Beck Depression Inventory (BDI) assesses suicidal thoughts or wishes. The possible scores for this item are 0, 1, 2, or 3, corresponding to different levels of severity. A score of 0 indicates no suicidal thoughts, while higher scores indicate increasing severity of suicidal ideation.

  2. Change in Mindfulness-Based Program - Meditation-Related Adverse Effects Scale (MBP-MRAES)

    Time frame: week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    MBP-MRAES is an 11-item questionnaire which measures distressing experiences associated with meditation practice. The first ten items use a frequency-based scale with the following response options: Never, A few days to 1 week, 1 week to 1 month, 1 month to 1 year, and 1 year or longer. If a participant selects any response other than Never, they are prompted with a follow-up question asking them to rate the experience on a scale from Very distressing to Very positive. The eleventh item is an open-ended question that invites participants to describe any other significant symptoms they may have experienced.

  3. Lasting Effects Questionnaire

    Time frame: 3-month follow-up (up to 4 months on study)

    An item about lasting bad effects from the HMP app will be scored on a 5-point scale from 1 = strongly disagree to 5 = strongly agree.

  4. Medication and Therapy Questionnaire

    Time frame: Baseline, week 4 (of intervention period), and 3-month follow-up (up to 4 months on study)

    The 3-item Medication and Therapy Questionnaire collects information on whether participants received medication or therapy for mental health concerns in the past month. Each item is a yes/no question.

  5. Change in Meditation and App Usage

    Time frame: Baseline, week 4 (of intervention period), and 3-month follow-up (up to 4 months on study)

    The 5-item Meditation and App usage Questionnaire assesses participants' engagement with meditation-related activities over two timeframes: the past month (at Week 4) and the past three months (at the 3-month follow-up). Three items ask whether participants used a meditation app, meditated with others, or attended a meditation class or group. Two additional items gather details about the specific meditation app used and the frequency of its use.

  6. Hospitalization

    Time frame: Week 1, week 2, week 3, week 4 (of intervention period), and 3 month follow-up (up to 4 months on study)

    The hospitalization form collects participants' hospitalization history since last survey.

Study contacts

Contact information is provided by the study sponsor or research team.

Simon Goldberg, PhD

CONTACT

[email protected]

(608) 265-8986

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Collaborators

  • Templeton World Charity Foundation

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jul 4, 2025
Registry last updated
Dec 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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