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Schizophrenia / Schizoaffective DisorderIGNITENCT07593456

NST-SPARK Open-Label Phase 1 STTR (IGNITE)

A study testing NST-SPARK in people with Schizophrenia / Schizoaffective Disorder, run by North Shore Therapeutics, Inc. at 2 sites in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Schizophrenia Spectrum disorders (SSD) are among the most devastating psychiatric disorders. Prominent negative symptoms such as low motivation, anhedonia, asociality, and emotional flattening are experienced by up to 60% of individuals with SSD and are often considered to be the greatest contributors to functional… Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Schizophrenia / Schizoaffective Disorder
What is being tested?
NST-SPARK
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
2 sitesUnited States
Study dates
1 Mar 2027to 31 Aug 2028
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 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18-65 years
  • Diagnosis of schizophrenia, schizoaffective disorder, schizophreniform disorder or unspecified psychotic disorder
  • Clinically stable, defined as no acute positive psychotic symptom exacerbation or recent hospitalization or medication changes within the last month.
  • Moderate to severe negative symptoms: CAINS MAP subscale >17 (28).
  • Sufficient functioning and capacity to consent and participate in a longitudinal study.
  • Actively engaged in outpatient treatment.
  • Able and willing to use a smartphone and maintain internet connection during use (through wifi or data plan).

Who cannot join

  • Safety risk (e.g., suicide attempt or homicidal ideation within 12 weeks)
  • Issues that prevent subject from using the smartphone app: e.g., hearing, vision, or other relevant physical disability
  • IQ < 70 based on clinical and historical information
  • Cognitive impairment limiting engagement in study
  • Prominent mood symptoms as defined by active manic, hypomanic or depressive episode.
  • Has previously undergone cognitive behavioral therapy for psychosis or recovery-oriented cognitive therapy for negative symptoms.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

William Cronin, MBA contact

214-693-8614

bill@northshore.health

Moein Foroughi, MD contact

507-271-7146

mforoughi@northwell.edu

United States2 sites
  • Zucker Hillside Hospital

    Glen Oaks, New York, 11004

    Moein Foroughi, MD, 718-470-8100, mforoughi@northwell.edu

    Sunny X Tang, MD, 718-470-8267, stang3@northwell.edu

  • Perelman School of Medicine

    Philadelphia, Pennsylvania, 19104

    Daniel Wolf, MD, PhD, 215-573-3538, danwolf@pennmedicine.upenn.edu

    Christian Kohler, MD, 215-573-3538, kohler@pennmedicine.upenn.edu

Other trials in United States

About this study

Official title: Investigating a Gamified NegatIve-symptom Therapeutic Based on Evidence-based Cognitive Therapy (IGNITE)

Schizophrenia Spectrum disorders (SSD) are among the most devastating psychiatric disorders. Prominent negative symptoms such as low motivation, anhedonia, asociality, and emotional flattening are experienced by up to 60% of individuals with SSD and are often considered to be the greatest contributors to functional disability. Currently, there are no FDA-approved or cleared medications or therapeutics targeting negative symptoms of schizophrenia. In this phase I proposal, North Shore Therapeutics (NST) is collaborating with the Feinstein Institutes of Medical Research (FIMR; Northwell Health) and the University of Pennsylvania (Penn) to develop a novel augmented reality (AR) therapeutic (NST-SPARK) targeting negative symptoms in individuals with SSD. NST-SPARK is a smartphone application that delivers Recovery-oriented Cognitive Therapy (CT-R) via gamified AR experiences to provide experiential learning that dismantles maladaptive beliefs. Preliminary findings suggest that this approach is feasible, acceptable, and may reduce defeatist beliefs associated with negative symptoms. NST-SPARK v.2.0 is being developed in partnership with a lived experience advisory panel. NST-SPARK v2.0 will deliver a 12-week course of treatment and will be developed over 10 development sprints spanning 9 months. In the second phase, the investigators will introduce NST-SPARK v2.0 to individuals with SSD (n=30) and moderate to severe negative symptoms for 12 weeks in a single-arm open-label study. The primary outcome is the efficacy of NST-SPARK v.2.0 in reducing experiential negative symptoms. Secondary outcomes include efficacy in reducing defeatist beliefs; efficacy in improving functioning; user statistics quantifying adherence to the prescribed sessions; qualitative, semi-structured feedback to guide future product development. This study will set the stage for FDA-informed phase II trials.

Read the detailed description

The investigators will evaluate NST-SPARK v2.0 in a 12-week, single-arm, open-label clinical trial in 30 individuals with schizophrenia spectrum disorders (SSD) who exhibit moderate to severe negative symptoms. Participants will be recruited from stable outpatient populations at Zucker Hillside Hospital (n=20) and the University of Pennsylvania (n=10). The primary objective of the study is to assess the feasibility and acceptability of NST-SPARK, along with generating preliminary evidence of efficacy in reducing experiential negative symptoms. Secondary objectives include evaluating changes in defeatist beliefs, effort expenditure, affect, global functioning, and overall symptom burden, as well as characterizing user engagement and collecting qualitative feedback to inform future product development. The investigators hypothesize that NST-SPARK will demonstrate strong feasibility and acceptability, defined by mean Acceptability of Intervention Measure (AIM) and Feasibility of Intervention Measure (FIM) scores greater than 3.5, and adherence exceeding 75% of prescribed sessions. The investigators further expect to observe moderate improvements in experiential negative symptoms and reductions in defeatist beliefs. Eligible participants will be adults aged 18 and older with a diagnosis of schizophrenia, schizoaffective disorder, schizophreniform disorder, or unspecified psychotic disorder. All participants must be clinically stable, with no recent exacerbation of positive symptoms, hospitalization, or medication changes within the prior month. Participants must exhibit moderate to severe negative symptoms, defined by a CAINS Motivation and Pleasure (MAP) subscale score greater than 17, and must have sufficient cognitive and functional capacity to consent and participate in a longitudinal study. Participants will be excluded if they present a significant safety risk (including recent suicidal or homicidal ideation), have impairments that would prevent use of a smartphone-based intervention (e.g., severe sensory or physical limitations), have an estimated IQ below 70, or demonstrate cognitive or psychiatric conditions that would limit engagement (including active mood episodes such as mania or major depression). Participants will access NST-SPARK either on their personal compatible smartphone or on a study-provided device. A trained research coordinator at each site will support onboarding, conduct assessments, and provide technical assistance. Outcome assessments will be conducted by centralized raters blinded to study conditions for key endpoints. Participants will be instructed to engage with the application at least three times per week over the 12-week treatment period, with the option for more frequent use. Based on prior experience in this population, approximately 20 participants are anticipated to complete the study. Study activities will begin with a screening phase to confirm eligibility, followed by baseline assessments prior to initiating treatment. Participants will then complete interim follow-up assessments at weeks 3, 6, and 9, and a final endpoint assessment at week 12. Recruitment will begin after finalization of the NST-SPARK v2.0 platform, with enrollment occurring over approximately 10 months at a rate of 3-4 participants per month. This will be followed by a three-month period for completion of follow-up assessments and an additional three months for data analysis, manuscript preparation, and planning of a subsequent Phase II study. Input from individuals with lived experience will be incorporated throughout the trial to contextualize findings and inform future study design. Participants will undergo a comprehensive assessment battery spanning diagnostic, symptomatic, behavioral, and functional domains. Diagnostic eligibility will be confirmed during screening using structured clinical interviews focused on mood and psychotic disorders, with additional screening to exclude individuals with significant depressive symptoms. All analyses will be conducted on available data regardless of adherence to the intervention. Given the exploratory nature of this early-stage study, adjustments for multiple comparisons will not be applied. Approximately 20 participants are anticipated to complete the study after accounting for expected attrition. This sample size provides sufficient statistical power to detect moderate treatment effects in within-subject analyses. Key indicators of success include demonstration of strong feasibility and acceptability, meaningful engagement with the intervention, and at least moderate improvement in experiential negative symptoms. In addition, successful completion of this study is expected to yield a trial-ready version of NST-SPARK capable of delivering a full 12-week therapeutic experience, incorporating both cognitive-behavioral and augmented reality components.

Being tested
NST-SPARK
Keywords
schizophrenia, recovery-oriented cognitive therapy (CT-R), cognitive behavioral therapy (CBT), prescription digital therapeutic, software as a medical device (SaMD), augmented reality (AR), negative symptoms, avolition
Medical subject headings
Schizophrenia, Psychotic Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • NST-SPARKDevice

    NST-SPARK v2.0 is a smartphone-based digital therapeutic that delivers recovery-oriented cognitive therapy (CT-R) through gamified augmented reality (AR) experiences to treat negative symptoms of schizophrenia spectrum disorders. Over a 12-week course, participants complete interactive sessions on their smartphone in which the app guides them to (1) identify targeted defeatist beliefs, (2) engage in brief AR activities featuring encouraging prompts and game-like challenges such as sorting objects, (3) reflect on the experience through guided cognitive restructuring, and (4) generalize insights to real-life goal-directed activities. Gamification elements including points, rewards, and progress tracking are integrated throughout to enhance engagement and reinforce effort. NST-SPARK is added to treatment as usual with no changes to participants' existing pharmacotherapy or clinical visits.

Study groups in NCT07593456
Study groupRoleWhat they receive
NST-SPARK v.2.0ExperimentalNST-SPARK v2.0 is a smartphone-based, software-as-a-medical-device digital therapeutic. It comprises 12 weeklong modules, and participants use the app on a personal or study-provided smartphone at least three times weekly over 12 weeks.
Receives: Device: NST-SPARK

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Experiential negative symptoms

    Experiential negative symptoms include avolition, asociality and anhedonia and will be assessed with the Motivation and Pleasure (MAP) subscale of the Clinical Assessment Interview for Negative Symptoms (CAINS). The MAP scale as an aggregate measure adds together the 9 individual items each ranging from 0 to 4; as an aggregate measure, the CAINS-MAP score ranges from 0 to 36 with 36 representing greater symptom severity.

    Measured: This measure will be collected at baseline and at the 12-week endpoint.

  2. Acceptability

    Acceptability of NST-SPARK v.2.0 will be assessed with the Acceptablilty of Intervention Measure self-report scale (AIM). The AIM consists of 4 items, each scored on a 5-point Likert scale (1 = Completely Disagree to 5 = Completely Agree). The score is reported as the mean of the 4 items, ranging from 1 to 5. Higher scores indicate greater acceptability (better outcome).

    Measured: This measure will be collected at the 12-week endpoint.

  3. Feasibility

    Feasibility of NST-SPARK v.2.0 will be assessed with the Feasibility of Intervention Measure self-report scale (FIM). The FIM consists of 4 items, each scored on a 5-point Likert scale (1 = Completely Disagree to 5 = Completely Agree). The score is reported as the mean of the 4 items, ranging from 1 to 5. Higher scores indicate greater perceived feasibility (better outcome).

    Measured: This measure will be collected at the 12-week endpoint.

Secondary outcomes (8)
  1. Global Functioning

    Global role and social functioning will be assessed with the Global Functioning (GF) scales from Cornblatt et al. Global role and social functioning will be assessed with the Global Functioning (GF) scales from Cornblatt et al. Each scale is a single-item rating scored from 1 to 10. Higher scores indicate better functioning (better outcome).

    Measured: This measure will be collected at baseline and at the 12-week endpoint.

  2. Defeatist Beliefs

    Defeatist performance beliefs will be assessed with the Beck Defeatist Belief Scale (DBS) self-report. The DBS consists of 15 items, each scored on a 7-point Likert scale (1 = Disagree Totally to 7 = Agree Totally).The score is reported as the total across all 15 items, which ranges from 15 to 105. Higher scores indicate stronger defeatist beliefs (worse outcome). In addition, we will report factor scores for Overvaluing Success (6 items), Overvaluing Failure (7 items), and Overvaluing Social Evaluation (3 items). Factor scores will be reported as a mean item score for that factor from 1 to 7.

    Measured: This measure will be collected at baseline, during the interim 3-, 6-, and 9-week timepoints, and at the 12-week endpoint.

  3. Positive Self Regard

    Positive self regard will be assessed with the Oxford Positive Self (OxPos) self-report scale. There are 24 items rated as a likert scale (0=Do not believe it, 4=believe it totally). The OxPos score will be reported as a total score, which ranges from 0 - 96, with higher score indicating better positive self regard (good outcome). In addition, we may explore the factor scores for Mastery, Strength, Enjoyment, and Character which each range from 0-28.

    Measured: This measure will be collected at baseline, during the interim 3-, 6-, and 9-week timepoints, and at the 12-week endpoint.

  4. Effort Expenditure

    Objective effort expenditure will be measured using a computerized verison of the Progressive Ratio Test (PRT). The primary outcome is the breakpoint, defined as the maximum effort a participant is willing to exert for a given reward. There are no fixed minimum and maximum scale values in the traditional sense; breakpoint values are continuous and depend on task parameters. Higher breakpoints indicate greater motivation (better outcome).

    Measured: This measure will be collected at baseline, during the interim 3-, 6-, and 9-week timepoints, and at the 12-week endpoint.

  5. Loneliness

    Loneliness will be assessed via self-report with the UCLA Loneliness Scale short form (UCLA-LS-3). The UCLA-LS-3 (3-item version) consists of 3 items, each scored on a 3-point scale (1 = Hardly Ever to 3 = Often). Total scores range from 3 to 9. Higher scores indicate greater loneliness (worse outcome).

    Measured: This measure will be collected at baseline and at the 12-week endpo

  6. Overall Psychosis Symptoms

    Overall psychosis symptoms will be assessed with the COMPASS Clinician Rating Form developed for the RAISE-ETP study (COMPASS-10). The COMPASS-10 consists of 10 items. Each item is scored on a scale from 0 to 7, yielding a total score range of 0 - 60. Higher scores indicate more severe psychosis symptoms (worse outcome).

    Measured: This measure will be collected at baseline and at the 12-week endpoint.

  7. Qualitative Feedback on App Experience

    Qualitative feedback will be collected for NST-SPARK through a semi-structured interview. These results will be reported descriptively, using quotes and summaries of the participants' responses.

    Measured: This measure will be collected at the 12-week endpoint.

  8. Vocal Biomarker Composite Score

    Vocal biomarkers composite score for negative symptoms will be extracted from recorded clinical assessments with the centralized rater. Assessments with the CAINS, GF, and COMPASS-10 will be used. The vocal biomarkers will be scored via a single composite z-score benchmarked against external datasets. The composite will be based on external data, compiling which biomarkers are associated with negative symptoms. The definitive way the score will be compiled is still pending ongoing independent studies at this time. There is no minimum or maximum score. Higher score means that the vocal features are more aligned with the expected phenotype for negative symptoms (greater severity).

    Measured: This measure will be collected at baseline and at the 12-week endpoint.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 May 2026
  2. Study start1 Mar 2027 (estimated)
  3. Primary completion28 Feb 2028 (estimated)
  4. Study completion31 Aug 2028 (estimated)

Resources

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
Not applicable
Intervention model
Single group
Model description
This is an open-label, single-arm, minimal risk clinical trial for a digital therapeutic app that provides recovery-oriented cognitive therapy targeting negative symptoms of schizophrenia spectrum disorders.
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07593456
Sponsor's protocol ID
NST-SPARK-Phase1
Other IDs
R41MH140642-01A1
Acronym
IGNITE
Status last verified
May 2026
First submitted
5 May 2026
Last updated
18 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
Undecided: Not required for NIMH Phase 1 STTR, but we may shared fully deidentified metadata as a part of the peer-review process for resulting publications.

Publications

  • Tang SX, Foroughi M, Brinen AP, Birnbaum ML, Berretta SA, Behbehani LM, Kane JM, Yoon E, Cronin WF. Preliminary Findings From an Augmented Reality (AR) App Delivering Recovery-Oriented Cognitive Therapy for Negative Symptoms in Schizophrenia. Early Interv Psychiatry. 2026 Jan;20(1):e70119. doi: 10.1111/eip.70119.

    PubMed 41496485

Questions about this trial

What is this clinical trial studying?

A study testing NST-SPARK in people with Schizophrenia / Schizoaffective Disorder, run by North Shore Therapeutics, Inc. at 2 sites 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 7 inclusion and 6 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: opening soon, as of the sponsor's last update on 18 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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?

Contact William Cronin, MBA (214-693-8614, bill@northshore.health), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Experiential negative symptoms (time frame: This measure will be collected at baseline and at the 12-week endpoint.). 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?

On the ClinicalTrials.gov record for NCT07593456, which also lists 1 linked publication.

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 18 May 2026.

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