iTEST Program for Schizoaffective Disorder
Randomized Clinical Trial of iTEST: A Blended Intervention Targeting Introspective Accuracy
Recruiting
N/A
Interventional Study
Schizophrenia Disorders
Schizoaffective Disorder
Psychotic Disorder
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 201 (estimated)
- Sponsor
- University of California, San Diego · Other
Who this trial is looking for
This trial is looking for adults with schizophrenia or schizoaffective disorder. Participants will use a mobile device for cognitive training and receive coaching over 12 weeks.
Are You a Good Fit for This Trial?
You may be able to join if
- I am between 18 and 65 years old.
- I have a diagnosis of schizophrenia or schizoaffective disorder.
- I can read at least at a 6th grade level.
- I have not been hospitalized or changed my medications in the last 2 months.
- I have someone who can support me monthly.
- I am not fully employed or responsible for my household.
You may not be able to join if
- I have severe disorganization in my thinking.
- I have had substance dependence in the past 3 months.
- I need care that prevents me from attending therapy.
- I cannot see or use a smartphone properly.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your Eligibility
About This Trial
The purpose of this study is to evaluate the effectiveness of a psychosocial intervention called iTEST for people with psychotic disorders that targets introspective accuracy, or the ability to accurately gauge ones abilities. iTEST combines daily cognitive training on a mobile device with coaching that addresses recovery goals. In this trial, we will randomize people to one of two interventions c…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Voluntary informed consent to participate and capacity to consent as measured by the UCSD Brief Assessment of Capacity to Consent (UBACC)
2. Age 18 to 65;
3. DSM-5 diagnosis of schizophrenia or schizoaffective disorder based on a structured diagnostic interview and available …
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