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Completed Not applicable Interventional Results available

Assessing Effectiveness and Implementation of an EHR Tool to Assess Heart Health Among Survivors

ClinicalTrials.gov ID: NCT03935282

Public ClinicalTrials.gov record NCT03935282. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 3:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Assessing Effectiveness and Implementation of an EHR Tool to Assess Heart Health Among Survivors (AH-HA)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this hybrid effectiveness-implementation study is to examine the effects of an EHR-based cardiovascular health assessment tool (AH-HA) among breast, prostate, colorectal, endometrial, and Hodgkin and non-Hodgkin lymphoma cancer survivors (N=600) receiving survivorship care in community oncology practices, using a group-randomized trial design (6 intervention practices and 6 usual care practices). Our central hypothesis is that the AH-HA tool will increase (1) cardiovascular health (CVH) discussions among survivors and oncology providers, (2) referrals and visits to primary care and cardiology (care coordination), and (3) cardiovascular (CV) risk reduction and health promotion activities compared to usual care.

Study identification

NCT ID
NCT03935282
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
645 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2020
Primary completion
Mar 6, 2025
Completion
Nov 16, 2025
Last update posted
Apr 14, 2026

2020 – 2025

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
Mercy Hospital Fort Smith Fort Smith Arkansas 72903
Oncology Associates at Mercy Medical Center Cedar Rapids Iowa 52403
Saint Louis Cancer and Breast Institute-Ballwin Ballwin Missouri 63011
Mercy Hospital Springfield Springfield Missouri 65804
Mercy Hospital Saint Louis St Louis Missouri 63141
Mercy Hospital Oklahoma City Oklahoma City Oklahoma 73120
Community Medical Center Scranton Pennsylvania 18510
Geisinger Wyoming Valley/Henry Cancer Center Wilkes-Barre Pennsylvania 18711
Baptist Memorial Hospital and Cancer Center-Memphis Memphis Tennessee 38120
Baptist Memorial Hospital for Women Memphis Tennessee 38120
Virginia Commonwealth University/Massey Cancer Center Richmond Virginia 23298
ThedaCare Regional Cancer Center Appleton Wisconsin 54911

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03935282, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 14, 2026 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03935282 live on ClinicalTrials.gov.

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