Assessing Effectiveness and Implementation of an EHR Tool to Assess Heart Health Among Survivors (AH-HA)
Breast Neoplasm, Prostatic Neoplasm, Colorectal Neoplasms
About this trial
This is an interventional supportive care trial for Breast Neoplasm focused on measuring Cardiovascular risk, Cardiovascular disease, Cancer, Survivor, Health Behaviors, Oncology Providers, EHR, Informatics
Eligibility Criteria
Inclusion Criteria:
- >= 6 months post-potentially curative cancer treatment for breast, prostate, colorectal, or endometrial cancers or Hodgkin and non-Hodgkin lymphomas. Ongoing hormonal therapies such as tamoxifen, aromatase inhibitors (with or without adjuvant CDK 4/6 inhibitors such as abemaciclib), or androgen deprivation are allowed.
- Scheduled for a routine cancer-related follow-up care visit within the next 30 days with a provider who received training to use AH-HA.
- Able and willing to complete a follow-up assessment in one year.
- Survivors must have no evidence of disease at the time of last medical visit for all cancers, except non-melanoma skin disease.
- Age >= 18 years.
- Able to understand and willing to provide verbal informed consent.
Exclusion Criteria:
- Survivors will be excluded if they have a history of cancer recurrence for any cancer other than non-melanoma skin disease.
- Prostate patients on active surveillance will be excluded.
- Survivor does not speak English or Spanish.
- Survivors who are currently on another interventional protocol in which cardiovascular risk factors (e.g., blood pressure, smoking, diet, physical activity) are being addressed, as per patient self-report or research staff members' knowledge at the time of consent.
Sites / Locations
- Mercy Hospital Fort Smith
- Oncology Associates at Mercy Medical Center
- Saint Louis Cancer and Breast Institute-Ballwin
- Mercy Hospital Saint Louis
- Mercy Hospital Springfield
- Mercy Hospital Oklahoma City
- Community Medical Center
- Geisinger Wyoming Valley/Henry Cancer Center
- Baptist Memorial Hospital and Cancer Center-Memphis
- Baptist Memorial Hospital for Women
- Virginia Commonwealth University/Massey Cancer Center
- ThedaCare Regional Cancer Center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Intervention - AH-HA tool
Usual Care
With assistance from the study team, the clinic will implement the AH-HA tool in the clinics' EPIC EHR. Providers at the intervention sites will be trained to use the tool during routine follow-up care with survivors. During a routine follow-up care appointment, the provider will use the AH-HA tool with enrolled patients.
Usual care practices will conduct routine follow-up care visits for enrolled survivors following typical clinic practice, without use of the AH-HA tool.