A Study to Evaluate the Overall Effects of Treatment With Abbreviated CT-156 in People With Schizophrenia

NCT06136936 | Completed FDA Device

• 1 other identifier: CT-156-C-001
• Study Type: interventional
• Target: 53
• Locations: 1 country
• Sites: 1

Brief Summary

An exploratory, double-arm, 4-week study to explore the feasibility and acceptability of abbreviated treatment with CT-156 for people with Schizophrenia.

Conditions

Schizophrenia

Keywords

Schizophrenia; Software as a Medical Device (SaMD); Smartphone app

Outcome Measures

Primary Outcomes (4)

• Number of days used

  Number of days the Study App is opened out of total days of treatment

  Day 0 to Week 4

• Number of times Study App is opened

  Number of times the Study App is opened during the treatment period

  Day 0 to Week 4

• Number of tasks completed

  Number of assigned tasks completed during the treatment period

  Day 0 to Week 4

• Length of time in App

  Length of each App-use session

  Day 0 to Week 4

Study Arms (2)

CT-156

ACTIVE COMPARATOR

Study app investigational treatment for adult patients diagnosed with schizophrenia.

Device: CT-156-C-001

CT-156 + UXR

EXPERIMENTAL

Study app investigational treatment for adult patients diagnosed with schizophrenia with up to five in-patient visits with three interviews for UXR (user experience research) arm.

Device: CT-156-C-001

Interventions

CT-156-C-001 DEVICE

CT-156 is a digital therapeutic (DTx) under development to treat patients 18 years of age and older with a diagnosis of schizophrenia under standard of care therapy who are on antipsychotic medication and not currently experiencing acute hallucinations or delusions.

CT-156; CT-156 + UXR

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• A participant will be eligible for entry into the study if all of the following criteria are met:
• Willing and able to provide written informed consent to participate in the study, attend study visits, and comply with study-related requirements and assessments.
• Is an adult at least 18 years of age at the time of informed consent.
• Fluent in written and spoken English, confirmed by ability to read and understand the informed consent form.
• Lives in the United States.
• Meets diagnostic criteria for a primary diagnosis of schizophrenia as defined in the International Classification of Diseases, Eleventh Edition (ICD-11) or Diagnostic Statistical Manual, Fifth Edition (DSM-5) for at least 6 months prior to screening.
• Has outpatient treatment status at the time of screening, with no psychiatric inpatient hospitalization within 13 weeks (3 months) prior to screening.
• Is currently prescribed at least one typical and/or atypical antipsychotic medication, and has been on the same antipsychotic medication(s) for at least 13 weeks (3 months) prior to randomization (Day 1). Dose adjustments are permitted during the study as outlined in the respective package insert(s).
• Has an average score of \>2 in at least 2 domains of Understanding and communicating, Getting Along with People, Life Activities - Household, or Participation in Society on the World Health Organization Disability Assessment Schedule 2.0 (WHO-DAS 2.0).
• Participant is the only user of an iPhone with iPhone operating system (iOS) version 14 or later or a smartphone with an Android operating system (OS) version 11 or later and agrees to download and use the digital mobile application as required by the protocol.
• Is willing and able to receive SMS text messages and push messages on their smartphone.
• Is the owner of and has regular access to an email address.
• Has regular access to the internet via cellular data plan and/or wi-fi.
• Has stable housing and has remained at the same residence for at least 13 weeks (3 months) prior to screening, and does not anticipate housing changes for the duration of the study.
• Understands the use of the Study App during the screening period and at the Baseline Visit, per investigator judgment.

You may not qualify if:

• A participant will not be eligible for study entry if any of the following criteria are met:
• Has acute prominent positive symptoms that, in the opinion of the investigator, would preclude effective engagement with the app
• Is currently receiving or has received concomitant therapy, defined as individual or group-based structured treatment (e.g., Cognitive Behavioral Therapy, Social Skills Training, Motivational Interviewing, or Vocational/Occupational Therapy), within 6 months (26 weeks) prior to screening per investigator assessment.
• Is currently treated with more than two antipsychotic medications (including more than 2 dosage forms).
• Is currently treated with clozapine, or was treated with clozapine within 5 years of the Screening Visit.
• Meets ICD-11 or DSM-5 criteria for diagnoses not under investigation that will impact compliance to the protocol, including schizophreniform, schizoaffective, or psychosis non-specific disorders (post-traumatic stress disorder \[PTSD\], bipolar disorder, major depressive disorder, developmental disorders).
• Meets ICD-11 or DSM-5 criteria for a current episode of depression, mania or hypomania.
• Meets ICD-11 or DSM-5 criteria for a current substance or alcohol use disorder (excluding caffeine and nicotine) within 26 weeks (6 months) of the Screening Visit. Diagnoses classified as in sustained remission are permitted.
• In the investigator's opinion, currently needs or will likely require prohibited concomitant medications and/or therapy during the study.
• Is at risk for suicide, as defined by any of the following:
• A "yes" response to either item 4 or 5 on the C-SSRS Suicidal Ideation Items within the last 13 weeks (3 months) prior to screening or at the Baseline Visit.
• A "yes" response on the C-SSRS Suicidal Behavior Items within the last 26 weeks (6 months) prior to screening or at the Baseline Visit.
• In the opinion of the investigator, presents a serious risk of suicide.
• Has participated in another clinical study (interventional or observational) in the last 26 weeks (6 months).
• Has previously participated in study CT-155-C-001, CT-155-C-002, CT-155-C-003, CT-155-P-00x, or CT-155-A-001.

Sponsors & Collaborators

• Click Therapeutics, Inc.: lead
• Boehringer Ingelheim: collaborator

Study Sites (1)

Click Therapeutics

New York, New York, 10013, United States

Location

MeSH Terms

Conditions

Schizophrenia

Condition Hierarchy (Ancestors)

Schizophrenia Spectrum and Other Psychotic Disorders; Mental Disorders

Study Officials

• Shaheen Lakhan

  Click Therapeutics

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: DEVICE FEASIBILITY
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 3, 2023
• First Posted: November 18, 2023
• Study Start: September 20, 2023
• Primary Completion: January 18, 2024
• Study Completion: February 22, 2024
• Last Updated: May 1, 2025

Record last verified: 2025-04

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)