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PreView: The Preventive Video Education in Waiting Rooms Program

University of California San Francisco (UCSF) logo

University of California San Francisco (UCSF)

Status

Completed

Conditions

Health Status Unknown

Treatments

Other: Questionnaire Administration
Other: Computer-Assisted Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02264782
NCI-2017-00456 (Registry Identifier)
14988 (Other Identifier)
R01CA158027 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This clinical trial studies how well PreView, preventive video education, works in increasing rates of breast, cervical and colorectal cancer screening, improving participants' stage of change with respect to age appropriate cancer screening and increasing patient-provider discussions about prostate cancer screening.

Full description

PRIMARY OBJECTIVES:

I. To determine the extent to which PreView increases the likelihood that primary care patient participants will receive mammograms, pap tests, colon cancer tests or prostate specific antigen (PSA) testing discussions with primary care physicians compared with participants who receive usual care.

II. To determine the extent that PreView increases participants' readiness to be screened for breast cancer, cervical cancer or colorectal cancer (CRC) compared with usual care.

III. To determine the extent that PreView increases the likelihood that PSA testing will be discussed in primary care physician visits compared with usual care.

OUTLINE: Patients are randomized into 1 of 2 groups.

GROUP I: Patients complete PreView, the Video Doctor plus Provider Alert, over 45 minutes on an iPad in the waiting room before a doctor visit.

GROUP II: Patients watch a video about healthy lifestyles including information about exercise and healthy eating over 45 minutes on an iPad in the waiting room before a doctor visit.

Enrollment

508 patients

Sex

All

Ages

50 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Without a history of cancer

Exclusion criteria

  • With a history of cancer (for whom subsequent procedures would be surveillance and not screening)
  • Individuals who do not speak English or Spanish (except for the testimonials)

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

508 participants in 2 patient groups

Group I (PreView)
Experimental group
Description:
Patients complete PreView, the Video Doctor plus Provider Alert, over 45 minutes on an iPad in the waiting room before a doctor visit.
Treatment:
Other: Computer-Assisted Intervention
Other: Computer-Assisted Intervention
Other: Questionnaire Administration
Group II (educational video)
Active Comparator group
Description:
Patients watch a video about healthy lifestyles including information about exercise and healthy eating over 45 minutes on an iPad in the waiting room before a doctor visit.
Treatment:
Other: Computer-Assisted Intervention
Other: Computer-Assisted Intervention
Other: Questionnaire Administration

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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