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Completed

NCT Number: NCT05603923

Study of a PST-Trained Voice-Enabled Artificial Intelligence Counselor(SPEAC) for Adults With Emotional Distress (Phase 2)

Approximately 200 Participants with mild-to-moderate, untreated depression and/or anxiety will be randomly assigned (by chance, like flipping a coin) to 1 of 3 study groups: Lumen Coached Problem-Solving Treatment (PST) (n=100), Human Coached PST (n=50), and optional (delayed) Lumen Coached PST as waitlist control (n=50) to improve emotional health. All participants will complete assessments at baseline and at 18 weeks post randomization.

Depending on the group assignment the PST program will be delivered by Lumen, a virtual voice-based coach on a study iPad, or by a human coach in person for the first session and then via videoconference or phone for the remaining 7 sessions. Participants assigned to the waitlist control group can receive the Lumen coached PST on a study iPad after completing their 18-week follow-up assessment.

Participants will receive 8 coaching sessions to learn problem-solving skills and work on unresolved problems in daily living that may be interfering with their emotional well-being and contributing to depression and anxiety symptoms.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Medicine, Vitoux Program on Aging and Prevention, Chicago, Illinois, United States

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About this study

All participants will complete measurements of neural target engagement and treatment outcomes at both baseline (0 week) and 18 weeks.

Study Visit 1: This will include (1) Physical measurements such as height, weight, and blood pressure, (2) functional magnetic resonance imaging (fMRI) scan, (3) surveys of intervention-related measures, and (4) surveys of patient-reported outcomes, such as depressive and anxiety symptoms, social functioning, and health-related quality of life.

Following the successful completion of Visit 1 and all the surveys, participants will be randomly assigned (by chance, like flipping a coin) to 1 of 3 study groups, as described below.

Problem Solving Treatment (PST) Groups

Group 1: Lumen Coached Group :

Participants assigned to this group will attend an Intervention Orientation session to receive the Coach Lumen tutorial, a study iPad, and a Lumen Intervention Workbook. They will complete 8 PST sessions (4 weekly and then 4 biweekly) with Coach Lumen at home over 12 weeks.

Group 2: Human Coached Group Participants assigned to this group will receive a study iPad and Human-Coached Intervention Workbook, and will complete 8 PST sessions (4 weekly and then 4 biweekly) with a trained health coach over 12 weeks. They will complete the first session in person and then the remaining sessions via videoconference or phone.

Group 3: Optional (Delayed) Lumen Coached Group Participants assigned to this group may choose to attend a Lumen Orientation session to receive training and a study iPad to complete 8 PST sessions with Coach Lumen after completing their follow-up assessment at 18 weeks.

Regardless of the group assignment, participants will complete brief Nightly Mood Check-in surveys about their thoughts, feelings, and experiences over the day, for 7 nights, approximately every other week over 18 weeks (i.e., a total of 58 nights). These check-ins are sent via text message to their mobile phone.

Study Visit 2:

Regardless of group assignment, participants will be asked to attend a second in-person visit for data collection at 18 weeks. Like Visit 1, Visit 2 will include physical measurements, a brain scan (after a negative pregnancy urine test, if applicable), and online surveys (if not yet completed before the visit), and will last approximately 90 minutes.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age: ≥ 18 years
  • Emotional distress defined by elevated depressive (PHQ-9 scores 10-19) and/or anxious symptoms (GAD-7 scores 10-14)
  • Willing and able to provide informed eConsent and HIPAA authorization

Exclusion criteria

  • Unable to speak, read, or understand English for informed consent
  • Current pharmacotherapy or psychotherapy (individual or professionally led group therapy) for depression or anxiety (note: participants are not withdrawn post-randomization if they begin pharmacotherapy drugs or start psychotherapy during the study.)
  • Suicidal ideation per PHQ-9 with active plan
  • Bipolar or psychotic disorder, or current psychiatric treatment
  • Weight ≥325 pounds due to brain scanner constraints, MRI contraindications, traumatic brain injuries, and tumor or any other known structural abnormality in the brain
  • Severe medical condition (e.g., myocardial infarction or stroke or new cancer diagnosis in the past 6 months, end-stage organ failure, terminal illness) or residence in a long-term care facility
  • Diagnosis of cancer (other than non-melanoma skin cancer) that is/was active or treated with radiation or chemotherapy within the past year
  • Active alcohol or substance use disorder (including prescription drugs) based on the CAGE Questionnaire Adapted to Include Drugs (CAGE-AID)
  • Cognitive impairment based on the Callahan 6-item screener
  • Current or planned pregnancy or lactating (<6 months postpartum)
  • Participation in other investigational treatment studies that would significantly affect participation in this study, raise safety concerns, and/or confound outcomes (participant may be asked to provide the informed consent of the other study for final decision on exclusion by a study psychiatrist)
  • Family/household member of an already enrolled participant or of a study team member
  • Plan to move out of the Chicago area during the study period
  • Does not have reliable Wi-Fi Internet at home
  • Unwillingness to user personal mobile device to receive study text messages
  • Investigator discretion for clinical safety or protocol adherence reasons

Treatment and study plan

Lumen Coached PST Intervention.

Behavioral

Lumen Intervention Orientation. Participants in the Lumen intervention arm attend a Lumen orientation visit (60 minutes) during which they will be given a Lumen intervention tutorial and receive a study iPad, configured to limit access to only the Lumen intervention enabled on the device. Before leaving, participants are scheduled for the first PST session with Coach Lumen. At the end of each PST session, participants are prompted to schedule their next session with Coach Lumen. They receive automated reminder notifications 1 day prior to their next session, on the session day, and have the opportunity to make up missed sessions. As needed, Lumen intervention orientations can be done remotely.

Human Coached PST Intervention.

Behavioral

Participants in the human coached PST arm will serve as active treatment controls given the demonstrated efficacy of human coached PST in depression and anxiety. They will complete 8 PST sessions with a human coach; first session in-person and remaining sessions via videoconferencing (i.e., Zoom preferred; with phone calls allowed) on the same 4 weekly and then 4 biweekly schedule as that for Lumen participants. Participants will receive a study iPad to use for their PST sessions via zoom. Participants also complete the PHQ-9 and GAD-7 during each session. Participants will receive a certificate of completion.

Optional (delayed) Lumen Coached PST (Waitlist control).

Behavioral

Waitlist control participants will only complete assessments during the 18-week trial period. At the end of their 18-week assessment, they will have the option to complete 8 PST sessions on their assigned iPads.

Primary outcomes

  1. Change From Baseline Functional Magnetic Resonance Scan at 18 Weeks

    Time frame: Baseline, 18 weeks

    Two neural targets defined a priori, specifically activation of the amygdala for nonconscious threat-related emotional reactivity and activation of the dorsal lateral prefrontal cortex (DLPFC) for cognitive control will be assessed using fMRI. The right DLPFC is the primary neural target, while the left DLPFC and bilateral amygdala are secondary neural targets. In the facial emotion viewing paradigm, facial expression stimuli are standardized black and white photographs of 8 identities (4 female, 4 male) with evoked expressions of threat-related emotions (fear, anger), loss-related emotions (sadness) and reward-related emotions (happiness), along with neutral. For the Go-NoGo paradigm, the 'Go' and 'NoGo' stimuli are presented for 500 ms each with an inter-stimulus interval of 750 ms. The beta weight is a standardized regression coefficient. Positive beta weights mean greater activation, and Negative beta weights mean less activation in the specific brain region being monitored.

Secondary outcomes

  1. Change From Baseline Hospital Anxiety and Depression Scale (HADS) at 18 Weeks

    Time frame: Baseline, 18 weeks

    HADS, including 7 questions for anxiety and 7 questions for depression, measures self-reported anxiety and depression in a general medical population of patients. Each item on the questionnaire is scored from 0-3 and the score for either anxiety or depression ranges between 0 and 21 with the following categories: normal 0-7, mild 8-10, moderate 11-14, and severe 15-21. Total score for the entire scale (psychological distress) ranges from 0 to 42, with higher score indicating more distress.

  2. Change From Baseline Penn State Worry Questionnaire (PSWQ) at 18 Weeks

    Time frame: Baseline, 18 weeks

    Penn State Worry Questionnaire (PSWQ) is a self-reported, 16-item, Likert-type scale that measures the trait of worry. Each item is related on a 1-5 scale. The total score of the scale ranges from 16 to 80, with higher scores indicating higher trait worry.

  3. Change From Baseline Positive and Negative Affect Schedule (PANAS) at 18 Weeks

    Time frame: Baseline, 18 weeks

    Positive and Negative Affect Schedule (PANAS) consists of two 10-item self-reported scales to measure positive and negative affect. Each item asks about the extent one has felt a positive or negative feeling on a 5-point scale of 1 (not at all) to 5 (very much). Positive Affect scores can range from 10 - 50, with higher scores representing higher levels of positive affect. Negative affect scores can range from 10 - 50, with lower scores representing lower levels of negative affect.

  4. Change From Baseline Social Problem-Solving Inventory-Revised: Short Form (SPSI-R:S) at 18 Weeks

    Time frame: Baseline, 18 weeks

    Participants' problem solving abilities will be assessed using the Social Problem-Solving Inventory-Revised: Short Form (SPSI-R:S) that contains 25 items in the following 5 subscales: positive problem orientation (PPO), negative problem orientation (NPO), rational problem solving (RPS), impulsive/careless style (ICS), and avoidance style (AS). Each item is rated on a 5-point scale ranging from "not at all true of me" (0) to "extremely true of me" (4). The total problem-solving ability score=(PPO raw score/5)+(20- NPO raw score)/5+ (RPS raw score/5)+(20- ICS raw score)/5+(20- AS raw score)/5. It ranged from 0 to 20, with the higher score indicating more productive problem-solving skills. Subscales scores (PPO, NPO, RPS, ICS, and AS) are raw scores without reversal. They range from 0 to 20, with the higher scores indicating the more positive and negative orientation, and the more rational, impulsive/careless, and avoidance style, respectively.

  5. Change From Baseline Dysfunctional Attitudes Scale (DAS) at 18 Weeks

    Time frame: Baseline, 18 weeks

    Dysfunctional Attitudes Scale (DAS Form A) is a 40-item self-reported scale that measures the presence and intensity of dysfunctional attitudes. Each item is rated a 7-point Likert scale (7 = fully agree; 1 = fully disagree) for a total scale range of 40 to 280. The higher the sum of the 40-items, the more dysfunctional attitudes an individual possesses.

  6. Change From Baseline Sheehan Disability Total Score at 18 Weeks

    Time frame: Baseline, 18 weeks

    The Sheehan Disability Scale is a validated questionnaire that measures functional disability and is sensitive to treatment effects in clinical trials. Patients rate the extent to which their symptoms impair work/school, social, and family life on a visual analog scale from 0 to 10. Total score is the sum of the three separate scores on work/school, social, and family life. Total scores range 0-30, with higher scores indicating greater functional impairment.

  7. Change From Baseline Work Productivity and Activity Impairment Questionnaire (WPAI) at 18 Weeks

    Time frame: Baseline, 18 weeks

    The Work Productivity and Activity Impairment questionnaire (WPAI) consists of 6 questions: 1 = currently employed; 2 = hours missed due to health problems; 3 = hours missed other reasons; 4 = hours actually worked; 5 = degree health affected productivity while working (using a 0 to 10 Visual Analogue Scale (VAS)); 6 = degree health affected productivity in regular unpaid activities (VAS). The recall period for the questions 2 to 6 is 7 days. Four main outcomes can be generated from the WPAI-GH and expressed in percentages by multiplying the following scores by 100: 1) percent work time missed due to health = Q2/(Q2 + Q4) for those who were currently employed; 2) percent impairment while working due to health = Q5/10 for those who were currently employed and actually worked in the past 7 days; 3) percent overall work impairment due to health Q2/(Q2 + Q4) + ((1 - Q2/(Q2 + Q4)) × (Q5/10)) for those who were currently employed; 4) percent activity impairment due to health Q6/10 for all.

  8. Change From Baseline Daily Mood (Positive Affect and Negative Affect) at 18 Weeks

    Time frame: Baseline and every 2 weeks (i.e., on weeks 2, 4, 6, 8, 10, 12, and 18)

    Daily end-of-day assessments will be captured over a one-week period at baseline and every 2 weeks (i.e., on weeks 2, 4, 6, 8, 10, 12, and 18). Changes in weekly average from baseline to week 18 are reported below. During active treatment in the Lumen arm and the in-person PST arm, this will occur for 3 days prior to, the day of, and for 3 days after a scheduled PST session. For waitlist controls, this will occur for 7 days starting on Sunday of each assigned week. Daily mood will be measured using 8 mood items (0 = Not at all, 6 = Extremely), with 4 measuring positive affect and 4 measuring negative affect. Positive affect score is mean of item scores, with higher scores indicating more positive affect. Negative affect score is mean of item scores, with higher scores indicating more negative affect.

  9. Change From Baseline Daily Stress at 18 Weeks

    Time frame: Baseline and every 2 weeks (i.e., on weeks 2, 4, 6, 8, 10, 12, and 18)

    Daily end-of-day assessments will be captured over a one-week period at baseline and every 2 weeks (i.e., on weeks 2, 4, 6, 8, 10, 12, and 18). Changes in weekly average from baseline to week 18 are reported below. During active treatment in the Lumen arm and the in-person PST arm, this will occur for 3 days prior to, the day of, and for 3 days after a scheduled PST session. For waitlist controls, this will occur for 7 days starting on Sunday of each assigned week. Daily stress will be assessed by the question "how stressful was your day today" (0 = Not at all, 6 = Extremely).

  10. Change From Baseline Daily Appraisal at 18 Weeks

    Time frame: Baseline and every 2 weeks (i.e., on weeks 2, 4, 6, 8, 10, 12, and 18)

    Daily end-of-day assessments will be captured over a one-week period at baseline and every 2 weeks (i.e., on weeks 2, 4, 6, 8, 10, 12, and 18). Changes in weekly average from baseline to week 18 are reported below. During active treatment in the Lumen arm and the in-person PST arm, this will occur for 3 days prior to, the day of, and for 3 days after a scheduled PST session. For waitlist controls, this will occur for 7 days starting on Sunday of each assigned week. The appraisal question asks "To what degree were you able to accept your problem as normal or an expected part of everyday life?" (0 = Not at all, 6 = A great deal), which a higher score indicating a greater degree of ability to accept problem as normal or expected.

Other outcomes

  1. Patient Health Questionnaire (PHQ-9)

    Time frame: Weeks 1, 2, 3, 4, 6, 8, 10, 12

    PHQ-9 is a self-administered instrument for screening, diagnosing, monitoring, and measuring the severity of depression. It rates the frequency of symptoms as "0" (not at all) to "3" (nearly every day) and has been validated for use in primary care. The PHQ-9 total score ranges from 0 to 27 and is categorized as follows: None or minimal depression 0-4, Mild depression 5-9, Moderate depression 10-14, Moderately severe depression 15-19, and Severe depression 20-27. PHQ-9 will be administered before each PST session (in weeks 1, 2, 3, 4, 6, 8, 10, 12) in Luman and Human groups, and at the same schedule in the Waitlist group. Changes in PHQ-9 scores from session 1 to session 8 are reported below.

  2. Generalized Anxiety Disorder Scale (GAD-7)

    Time frame: Weeks 1, 2, 3, 4, 6, 8, 10, 12

    GAD-7 is a valid and reliable 7-question self-report measure assessing the severity of generalized anxiety symptoms over the past two weeks. Total scores range from 0 to 21, with higher scores indicating a greater degree of anxiety symptom severity. GAD-7 will be administered before each PST session (in weeks 1, 2, 3, 4, 6, 8, 10, 12) in Luman and Human groups, and at the same schedule in the Waitlist group. Changes in GAD-7 scores from session 1 to session 8 are reported below.

  3. User Experience Questionnaire-Short Version (UEQ-S)

    Time frame: After Lumen Session 1, Session 4, Session 8

    User Experience Questionnaire-Short version (UEQ-S) is a validated instrument containing 8 items from the 26 items of the original UEQ. UEQ-S measures user experience. From the UEQ-S survey, scale values were calculated by rescaling the survey responses to the range -3 to 3 and UEQ-S total score were calculated as mean of survey responses. UEQ-S total scores <-0.8 represented a negative evaluation, between -0.8 and 0.8 represented a neutral evaluation, and >0.8 represent a positive evaluation.

  4. Change in Adapted Working Alliance Inventory for Digital Coaching Interventions (WAI-Tech) From First PST Session in Week 1 to Eighth Session in 12 Weeks

    Time frame: After Lumen Session 1, Session 4, Session 8

    Adapted Working Alliance Inventory for digital coaching interventions (WAI-Tech) was based closely on the original 36-item WAI and uses a parallel set of 36 items rated on a 7-point scale (1 = "never" to 7 = "always") to measure the level of alliance between patient and digital coach along 3 domains: Task (12 items), Bond (12 items), and Goal (12 items). An overall score was calculated based on item means. A higher overall score reflected a greater treatment alliance.

Sponsors and collaborators

Lead sponsor

University of Illinois at Chicago

Other

Collaborators

  • National Institute of Mental Health (NIMH)
  • Penn State University
  • Stanford University
  • Washington University School of Medicine

Registry information

Acronym: SPEAC

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Nov 3, 2022
Registry last updated
Sep 23, 2026

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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