A Multicenter, Randomized, Double-Blind, Parallel-Group, Controlled, 16-week Study to Evaluate the Efficacy and Safety of a Digital Therapeutic (CT-155) as an Adjunct to Standard-of-Care Antipsychotic Therapy in Adult and Late Adolescent Participants with Experiential Negative Symptoms of Schizophrenia (CLICK study)

CLICK/CONVOKE is a 22-week double blind digital therapeutic study that examines the efficacy of CT-155 as an adjunct treatment for patients diagnosed with experiential negative symptoms of schizophrenia.  CT-155 is a novel PDT being developed by Click Therapeutics, Inc. (Click) and Boehringer Ingelheim (BI), collectively, the study “sponsor.” CT-155 delivers an interactive, software-based intervention for experiential negative symptoms of schizophrenia.

Study Length

22 weeks

Disorder/Condition

Schizophrenia

Inclusion Criteria

  • Outpatient,
  • 18 years of age or older,
  • fluent in written and spoken English,
  • Is on a stable dose of antipsychotic medication(s) for at least 12 weeks prior,
  • Is the sole user of an iPhone with an iPhone operating system (iOS) 14 or greater, or a smartphone with an Android operating system (OS) 10 or greater.

Study Description (brief)

CLICK/CONVOKE is a 22-week double blind digital therapeutic study that examines the efficacy of CT-155 as an adjunct treatment for patients diagnosed with experiential negative symptoms of schizophrenia.  CT-155 is a novel PDT being developed by Click Therapeutics, Inc. (Click) and Boehringer Ingelheim (BI), collectively, the study “sponsor.” CT-155 delivers an interactive, software-based intervention for experiential negative symptoms of schizophrenia.

Study Contact

For more information about this study, please contact Jadaera Lorenzo, MA, at (212) 866-2690 or Jadaera.Lorenzo@omh.ny.gov.

 

Exclusion Criteria

  • Is currently treated with more than two antipsychotic medications (including more than two dosage forms),
  • Is currently receiving or has received psychotherapy within 3 months prior,
  • has a current diagnosis of substance or alcohol use disorder.

Study Location

Research offices are at the MPC Outpatient clinic (125th street/Adam Clayton Powell Blvd).