Improving Cancer Screening Through A Tailored Technology-Based Intervention
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Colorectal Cancer
- Sponsor
- Medical University of South Carolina
- Locations
- 1
- Primary Endpoint
- Rate of successful completion of breast cancer screening noted via electronic health record having mammogram result for the patient.
- Status
- Withdrawn
- Last Updated
- 2 years ago
Overview
Brief Summary
The primary purpose of this research study is to contribute to generalized knowledge on how to increase screening for patients at risk of missing their recommended cancer preventive care by using a newly developed predictive model and analytic tool to improve shared decision-making for these patients. The goal of the clinical trial is to evaluate (prove) the effectiveness of this shared-decision making support tool developed in EPIC on the rate of recommended cancer screening in practice. It contributes to knowledge on what specific methods can increase patient adherence to recommended preventive care and reduce disparities.
Detailed Description
Patients seen at primary care practices, who have been pre-determined to have unmet screening requirements and have received standard of care with a QI tool, will be asked to complete an optional questionnaire electronically through a patient portal or via a link sent by text within a week of their visit, based on their preference. Only those who have indicated they agree to be contacted for research purposes will be contacted. Surveys will be distributed through REDCap so no identifying information will be contained in the answers. REDCap is a free, HIPAA compliant interface for building and managing online databases. Additionally, surveys will be sent via mail if the patient cannot be reached electronically. Survey responses received through the mail will not include any identifying information. Pre-paid return envelopes will be provided to preserve anonymity. Although a small proportion of South Carolina's population are primary Spanish speakers (about 4%), to be inclusive we want to ensure all materials are available in Spanish. To remove barriers to participation, those needing physical, hearing, and visual assistance will be able to review and complete documents at the time of their clinic visit with the assistance of trained study personnel. Invitations will continue to be sent out until 100 total patient responses are received per practice in the pragmatic trial, or 50 per practice in the pilot. Clinicians will also receive a survey to assess the tool. Recruitment for clinicians surveys will be done via email sent by the practice managers to the providers who have agreed to use the QI tool. Clinician assessments will be delivered electronically via a link delivery by email or text, or sent by mail, based on clinician preference. Respondents will be reimbursed for their time and effort. These assessments will be anonymous. Survey participation will be coded in order to provide compensation. Since data will be identified only by code numbers (participant IDs) the master list of those codes will be kept physically separate from the collected data.
Investigators
Vanessa Diaz
Professor
Medical University of South Carolina
Eligibility Criteria
Inclusion Criteria
- •women 50-74 years old
Exclusion Criteria
- •current breast cancer diagnosis, mastectomy
- •Colorectal Cancer Screening:
- •Inclusion Criteria: adults 50-74 years Exclusion Criteria: colorectal cancer diagnosis
- •Lung Cancer Screening:
- •Inclusion Criteria: adult 55-80 years old with 30 pack per year history who currently smoke or quit within the last 15 years.
- •Exclusion Criteria: lung cancer diagnosis
Outcomes
Primary Outcomes
Rate of successful completion of breast cancer screening noted via electronic health record having mammogram result for the patient.
Time Frame: Duration of the study, a total of five years.
Successful completion rate per practice involved, based on eligible patients.
Rate of successful completion of colorectal cancer screening noted via electronic health record having colonoscopy, fecal occult blood, or non invasive screening option result for the patient.
Time Frame: Duration of the study, a total of five years.
Successful completion rate per practice involved, based on eligible patients.
Rate of successful completion of lung cancer screening noted via electronic health record having low dose computed tomography of the chest result for the patient.
Time Frame: Duration of the study, a total of five years.
Successful completion rate per practice involved, based on eligible patients.
Secondary Outcomes
- Average score of patient experience and satisfaction as assessed via Likert scale survey.(Duration of the study, a total five years.)
- Average score of clinician experience and satisfaction as assessed via Likert scale survey.(Duration of the study, a total five years.)