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PreView: The Preventive Video Education in Waiting Rooms Program

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ClinicalTrials.gov Identifier: NCT02264782
Recruitment Status : Completed
First Posted : October 15, 2014
Last Update Posted : May 17, 2019
Sponsor:
Collaborator:
National Cancer Institute (NCI)
Information provided by (Responsible Party):
University of California, San Francisco

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Health Status Unknown Other: Computer-Assisted Intervention Other: Questionnaire Administration Not Applicable

Detailed 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.


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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 508 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Screening
Official Title: PreView: The Preventive Video Education in Waiting Rooms Program
Study Start Date : July 2013
Actual Primary Completion Date : February 2019
Actual Study Completion Date : March 2019

Arm Intervention/treatment
Experimental: Group I (PreView)
Patients complete PreView, the Video Doctor plus Provider Alert, over 45 minutes on an iPad in the waiting room before a doctor visit.
Other: Computer-Assisted Intervention
Complete PreView

Other: Questionnaire Administration
Ancillary studies

Active Comparator: Group II (educational video)
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.
Other: Computer-Assisted Intervention
Watch an educational video

Other: Questionnaire Administration
Ancillary studies




Primary Outcome Measures :
  1. Changing participants' readiness to be screened for breast, cervical and colorectal cancer [ Time Frame: Up to 3 hours from pre-visit to post-visit interview. ]
    To determine the extent to which PreView increases the likelihood that primary care patient participants will receive mammograms, Pap tests, colon cancer tests or PSA testing discussions with primary care physicians compared with participants who receive usual care

  2. Increasing physician-patient discussions about PSA screening measured by chart review [ Time Frame: Baseline up to 14 months ]
    To determine the extent that PreView increases participants' readiness to be screened for breast cancer, cervical cancer or CRC compared with usual care.

  3. Increasing rates of breast, cervical and colorectal cancer screening [ Time Frame: From Baseline up to 14 months ]
    To determine the extent that PRE-VIEW increases the likelihood that PSA testing will be discussed in primary care physician visits compared with usual care.



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Ages Eligible for Study:   50 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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)

Information from the National Library of Medicine

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): NCT02264782


Locations
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United States, California
John Muir Medical Center-Concord Campus
Concord, California, United States, 94520
UCSF Medical Center-Mount Zion
San Francisco, California, United States, 94115
Sponsors and Collaborators
University of California, San Francisco
National Cancer Institute (NCI)
Investigators
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Principal Investigator: Judith Walsh UCSF Medical Center-Mount Zion

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Responsible Party: University of California, San Francisco
ClinicalTrials.gov Identifier: NCT02264782     History of Changes
Other Study ID Numbers: 14988
NCI-2017-00456 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )
14988 ( Other Identifier: UCSF Medical Center-Mount Zion )
P30CA082103 ( U.S. NIH Grant/Contract )
R01CA158027 ( U.S. NIH Grant/Contract )
First Posted: October 15, 2014    Key Record Dates
Last Update Posted: May 17, 2019
Last Verified: May 2019