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NCT02264782 Clinical Trial

PreView: The Preventive Video Education in Waiting Rooms Program

Health Status Unknown Clinical Trial

Official title:
PreView: The Preventive Video Education in Waiting Rooms Program

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02264782
Other study ID # 14988
Secondary ID NCI-2017-0045614
Status Completed
Phase N/A
First received
Last updated
Start date July 2013
Est. completion date March 2019

Study information
Verified date July 2020
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 508
Est. completion date March 2019
Est. primary completion date February 2019
Accepts healthy volunteers No
Gender All
Age group 50 Years to 70 Years
Eligibility 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)

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Computer-Assisted Intervention
Complete PreView
• Computer-Assisted Intervention
Watch an educational video
• Questionnaire Administration
Ancillary studies

Locations
Country Name City State
United States John Muir Medical Center-Concord Campus Concord California
United States UCSF Medical Center-Mount Zion San Francisco California

Sponsors (2)
Lead Sponsor Collaborator
University of California, San Francisco National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Changing participants' readiness to be screened for breast, cervical and colorectal cancer 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 Up to 3 hours from pre-visit to post-visit interview.
Primary Increasing physician-patient discussions about PSA screening measured by chart review To determine the extent that PreView increases participants' readiness to be screened for breast cancer, cervical cancer or CRC compared with usual care. Baseline up to 14 months
Primary Increasing rates of breast, cervical and colorectal cancer screening To determine the extent that PreView increases the likelihood that PSA testing will be discussed in primary care physician visits compared with usual care. From Baseline up to 14 months
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