A Usability Study of a Smoking Cessation Decision Aid in People With a Recent First Episode of Psychosis
- Conditions
- SmokingPsychosis
- Registration Number
- NCT01399112
- Lead Sponsor
- Northwell Health
- Brief Summary
The investigators propose to recruit patients who have experienced a recent first episode of psychosis who have a chart diagnosis of Schizophrenia, Schizophrenifom, Schizoaffective Disorder, Psychosis NOS, or Bipolar I Disorder with psychotic features and self identify themselves as a current cigarette smoker. Aiding this population with smoking cessation is crucial as the majority of people with schizophrenia spectrum disorders (50-90%) smoke, which is leading to early mortality. While these individuals can benefit from standard evidence-based treatment, these treatments are underutilized. Web based programs, such as the EDSS and thetruth.com, can provide education and motivational tools to help people with a recent onset of psychosis use evidence-based smoking cessation treatments. This study aims to test these two web-based programs among young people with a recent episode of psychosis for usability and likeability and to explore whether use of these two programs will motivate users to seek smoking cessation treatment or to engage in other quitting behaviors in the month following use of the programs. Information gathered from this proposal will be used to help the researchers decide whether either of these two programs will be reasonable to include in a larger study of a comprehensive treatment for individuals with first episode psychosis.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 11
- Patients with clinical diagnoses of Schizophrenia, Schizophrenifom, Schizoaffective Disorder, Psychosis NOS, or Bipolar I Disorder with psychotic features
- Diagnosed with one of above diagnoses within the past five years
- Ages 15-30 years old.
- Self-identified current cigarette smokers
- 5th grade reading level
- Willing to be audio recorded.
- Willing and legally able to provide informed consent to participate in the study or have a guardian provide informed consent with assent of a minor
- Physically unable to use a computer with assistance.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method number of cigarettes smoked One month Self-report of number of cigarettes smoked at baseline and at one month follow-up
- Secondary Outcome Measures
Name Time Method Satisfaction Immediately (up to 10 minutes) following the use of one of the web-based programs. Immediately after using the assigned web-based program, the participant will be asked a series of questions regarding what they liked, did not like, found easy to use or found difficult to use when engaging with the computer program. These questions take approximately 5-10 minutes to answer.
Trial Locations
- Locations (1)
Zucker Hillside Hospital
🇺🇸Glen Oaks, New York, United States
Zucker Hillside Hospital🇺🇸Glen Oaks, New York, United States