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Patient Recall of Cancer Screening and Diagnosis

Case Comprehensive Cancer Center (Case CCC) logo

Case Comprehensive Cancer Center (Case CCC)

Status

Enrolling

Conditions

Breast Cancer
Prostate Cancer

Treatments

Other: Accessing personal medical records online via online portals

Study type

Interventional

Funder types

Other

Identifiers

NCT05014295
CASE1Z21

Details and patient eligibility

About

The purpose of this research is to try to better understand how much information relating to cancer screening and diagnoses that people can recall on their own and to better understand how to help people get better information. In this study, investigators will see if giving time or other resources help individuals remember more and more accurate details about their cancer screening and care.

Full description

This is a randomized controlled trial of an intervention to encourage use of online medical records for filling out a cancer screening, diagnosis and treatment questionnaire. Participants will be asked to self-report on cancer screening and treatment. They will then be asked the same questions again a week later.

The control group will have had one week to reflect on the questions, and investigators anticipate some influence of this on responses. The intervention group will be prompted about accessing their medical records from the major local health systems online, with links to directions provided by each hospital system. They will then be asked to fill out the same questionnaire.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosed with breast or prostate cancer within the last 10 years
  • have access to the internet with a working email address
  • reside in Northeast Ohio

Exclusion criteria

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Control Group
No Intervention group
Description:
Survey questions at baseline and at one week. The control group will have had one week to reflect on the questions, and investigators anticipate some influence of this on responses.
Intervention Group
Active Comparator group
Description:
The intervention group will be prompted about accessing their medical records from the major local health systems online, with links to directions provided by each hospital system. They will then be asked to fill out the same questionnaire.
Treatment:
Other: Accessing personal medical records online via online portals

Trial contacts and locations

1

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Central trial contact

Cheryl Thompson, PhD

Data sourced from clinicaltrials.gov

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