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Patient Recall of Cancer Screening and Diagnosis

Not Applicable
Recruiting
Conditions
Prostate Cancer
Breast Cancer
Interventions
Other: Accessing personal medical records online via online portals
Registration Number
NCT05014295
Lead Sponsor
Case Comprehensive Cancer Center
Brief Summary

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.

Detailed 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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention GroupAccessing personal medical records online via online portalsThe 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.
Primary Outcome Measures
NameTimeMethod
Completeness of surveyat 1 week (after second survey completed)

Completeness: For each survey, for each participant, investigators will count the number of "don't know" response rates. From this, investigators will calculate the percent completeness of the survey.

Accuracy of surveyat 1 week (after second survey completed)

Investigators will assess the inter-rater reliability between the first and second survey by calculating a Cohen's Kappa coefficient. Although not a perfect assumption, investigators will use the second survey as the reference. Number of changed answers on an individual level will be calculated, representing improved accuracy. Investigators do not anticipate many changes, and, again, this will not be normally distributed.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Case Comprehensive Cancer Center

🇺🇸

Cleveland, Ohio, United States

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