Smoking Cessation Clinical Trial
— iMDOfficial title:
Interactive Mobile Doctor (iMD) for Asian Smokers
Verified date | May 2020 |
Source | University of California, San Francisco |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The primary aim of the proposed study is to conduct a randomized controlled trial (RCT) to evaluate the efficacy of the Interactive Mobile Doctor (iMD) intervention targeting 150 Chinese-, Korean- or Vietnamese-speaking male patients who smoke daily and have a scheduled clinic visit at Asian Health Services primary care.
Status | Completed |
Enrollment | 172 |
Est. completion date | September 2019 |
Est. primary completion date | June 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - age 18 or older; - male; - English, Chinese- (Cantonese), Korean- or Vietnamese-speaking; - self-identified as ethnic Chinese, Korean, Vietnamese or Asian - current smoker as identified by EHR; - have an already scheduled provider visit at Asian Health Services; - smoke at least 1 cigarette daily in the last 7 days; and - unwilling or unavailable to participate the in study procedures (e.g., to complete a brief post-visit survey right after the visit or by phone) according to the group assignment Exclusion Criteria: - Have vision and/or hearing difficulty that prevents the participant from viewing or hearing the intervention video messages and/or completing the assessment in person or by telephone |
Country | Name | City | State |
---|---|---|---|
United States | Asian Health Services | Oakland | California |
Lead Sponsor | Collaborator |
---|---|
University of California, San Francisco | Asian Health Services |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | abstinence | 7-day point prevalent smoking abstinence biochemically verified by salivary cotinine | 6-month | |
Primary | quite attempt | self-reported 24-hour quit attempts | 6-month | |
Secondary | patient-provider discussion | self-reported by patient whether discussion on tobacco use took place at the intervention clinical encounter | immediate post-intervention | |
Secondary | EHR documented 5As | EHR progress notes documenting delivery of the clinical guideline | immediate post-intervention |
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