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CompletedNCT02197052Updated Jul 22, 2014

iScreen Study: Best Methods for Social Screening in Pediatric Caregivers

An observational study in Disclosure Rates of Social Needs, sponsored by University of California, San Francisco. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-07-22.

Sponsored by University of California, San Francisco · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
552
Ages
18 Years and older
Sex
All
01

Study summary

The goal is to better understand the social needs of a population seeking care in a large, urban children's hospital emergency department with a large Medicaid population. Consenting English and Spanish-speaking adult caregivers will be randomized to social screening via a face -to-face interview with a trained bilingual researcher or via a self-completed tablet-based survey. We hypothesize that there will be no difference in disclosure rates between the two screening formats for items other than highly sensitive items. For highly sensitive items we hypothesize disclosure rates will be higher for the self-completed tablet-based survey.

02

Conditions studied

  • Disclosure Rates of Social Needs
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In context

Lead sponsor

University of California, San Francisco is the lead sponsor of 2,132 studies on the registry; 375 are open to participants now.

Of its 262 completed or terminated interventional studies of FDA-regulated products, 196 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants were drawn from adult caregivers seeking treatment for a child in a fast track arm of a large, urban children's hospital emergency department in Oakland, CA (CHO ED Annex).

Inclusion criteria

  • Caregiver must by age 18 years or older accompanying a child less than 18 years old
  • Primary language English or Spanish
  • Familiar with the child's household environment

Exclusion criteria

Exclusion Criteria:

-

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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
552 participants (actual)
Patient registry
No

Groups and cohorts

  • 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.

06

What researchers measure

Primary outcomes

  1. Disclosure rates for social needs questions

    The difference in disclosure rates will be determined by comparing the two arms and determining significant differences for social needs variables.

    Time frame: At time point 1, when the subject is first assessed

07

Study locations

1 site
  • Children's Hospital Oakland
    Oakland, California 94618, United States
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References and documents

Publications

  • Gottlieb L, Hessler D, Long D, Amaya A, Adler N. A randomized trial on screening for social determinants of health: the iScreen study. Pediatrics. 2014 Dec;134(6):e1611-8. doi: 10.1542/peds.2014-1439. Epub 2014 Nov 3. PubMed 25367545 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 22, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02197052
Lead sponsor
University of California, San Francisco
Collaborators
UCSF Benioff Children's Hospital Oakland
Responsible party
Sponsor
First posted
Jul 22, 2014
Start date
Jun 2013
Primary completion
Aug 2013
Completion
Aug 2013
Last update
Jul 22, 2014

Study contacts

Laura M Gottlieb, MD, MPH
principal investigator · University of California, San Francisco

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2014. You cannot join it, but the record below documents what was studied.

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