iScreen Study: Best Methods for Social Screening in Pediatric Caregivers
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|ClinicalTrials.gov Identifier: NCT02197052|
Recruitment Status : Completed
First Posted : July 22, 2014
Last Update Posted : July 22, 2014
|Condition or disease|
|Disclosure Rates of Social Needs|
|Study Type :||Observational|
|Actual Enrollment :||552 participants|
|Official Title:||iScreen Study: Best Methods for Social Screening in Pediatric Caregivers|
|Study Start Date :||June 2013|
|Actual Primary Completion Date :||August 2013|
|Actual Study Completion Date :||August 2013|
Computer Based Survey Arm
Participants randomized to the computer based self-completed survey arm were issued a tablet computer to answer survey questions. All participants were encouraged to ask for technical assistance if needed at any point, and like in the face-to-face interviews, electronic survey could be re-initiated at the point of discontinuation after any interruption. Those in the tablet survey arm also could complete the survey in their preferred language and all were additionally given headsets so they could use audio assist with identical, pre-recorded questions in the selected language.
Face-to-face interview arm
Participants randomized to this condition were interviewed in-person by a fully bilingual (English-Spanish), bi-cultural research assistant trained in cultural humility, standard research protocols and interviewing practices. Interviews were conducted in clinical rooms in respondent's preferred language, were easily interrupted for medical care, and the survey could be re-initiated at the point of discontinuation after any interruption. Participant responses during face-to-face interviews were recorded by the research assistant on paper and later recorded electronically.
- Disclosure rates for social needs questions [ Time Frame: At time point 1, when the subject is first assessed ]The difference in disclosure rates will be determined by comparing the two arms and determining significant differences for social needs variables.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02197052
|United States, California|
|Children's Hospital Oakland|
|Oakland, California, United States, 94618|
|Principal Investigator:||Laura M Gottlieb, MD, MPH||University of California, San Francisco|