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Cardiac Rehabilitation for Patients Receiving Radiation Therapy for Thoracic Cancers

A Pilot Trial of Cardiac Rehabilitation for Patients Receiving Radiation Therapy for Thoracic Cancers

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04072393
Enrollment
24
Registered
2019-08-28
Start date
2021-01-15
Completion date
2024-05-15
Last updated
2024-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Esophageal Cancer, Hodgkin Disease, Hodgkin Lymphoma, Lung Cancer, Non-hodgkin Lymphoma, Sarcoma, Thoracic Cancer, Thymoma

Brief summary

Other than optimizing medical management of cardiac risk factors, and reducing radiotherapy (RT) dose to the heart, there currently exist no interventions to mitigate or reverse the adverse cardiac effects of RT. Aerobic exercise has been demonstrated to improve patient quality of life, cardiac outcomes, and cardiorespiratory fitness in patients with cancer receiving cardiotoxic systemic therapies, but the effects of aerobic exercise on patients at high risk for radiation induced heart disease (RIHD) is unknown. In addition, home-based cardiac rehabilitation has not been tested in patients with thoracic cancers.

Interventions

-Patients will be evaluated by the clinical team at The Heart Care Institute (HCI). They will receive a heart rate monitor, blood pressure monitor, and weight scale that they will take home with them. They will receive training on how to use the heart rate monitor and blood pressure monitor. They will receive training on how to record their exercises and weights in the teleHeart application by an exercise physiologist from HCI. Within 6 weeks of completion of standard of care radiation therapy or cytotoxic chemotherapy (whichever is last), they will be prescribed a course of home-based CR by a cardiologist at HCI and be instructed on the regimen by an exercise physiologist from HCI.

Sponsors

The Foundation for Barnes-Jewish Hospital
CollaboratorOTHER
Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pathologically confirmed or radiographically diagnosed non-small cell lung cancer, small cell lung cancer, esophageal cancer, Hodgkin lymphoma, non-Hodgkin lymphoma, sarcoma, thymoma, or left-sided breast cancer. * Planning to receive neo-adjuvant, adjuvant, or definitive radiation therapy to the thorax with curative intent. * Willing to participate in home-based cardiac rehabilitation program and be monitored remotely via smart phone application * Possess a smart phone or tablet capable of supporting teleHeart application * Willing and eligible to co-enroll in the Cardiovascular Toxicity in Cancer and Improvement in Recovery (SURVIVE) Registry Study (HRPO# 201801031). * At least 18 years of age. * ECOG performance status ≤ 2 * Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).

Exclusion criteria

* Presence of distant metastatic disease (except patients with lymphoma). * Life expectancy less than 6 months * Patient lives in skilled nursing facility, chronic care facility, nursing home, or palliative care or hospice facility * Unable to walk * Presence of significant cancer disease burden that would make patient unlikely to tolerate cardiac rehabilitation (CR) * Diagnosis of primary cervical esophageal cancer. * Presence of unstable angina. * Recipient of heart transplant. * Patient on cardiac transplant list or has a ventricular assist device * Patient's baseline weight \> 300 lbs (due to weight limitations of the scale and bioelectrical impedance device) * Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 14 days of study entry. * Other medical comorbidities that make the patient unable to participate in the CR program or other assessments involved with this study.

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of completing home-based CR after definitive radiation therapy in patients with thoracic cancer who have started the CR programThrough completion of cardiac rehabilitation for all patients enrolled (estimated to be 36 months)Feasibility of completion is defined as 75% of patients who start their first session of cardiac rehabilitation participating in at least 75% of prescribed home-based CR exercise sessions.

Secondary

MeasureTime frameDescription
Feasibility of home-based cardiac rehabiliation in all enrolled patients after definitive radiation therapy in patients with thoracic cancer.Through completion of cardiac rehabilitation for all patients enrolled (estimated to be 36 months)Feasibility is defined as 75% of all enrolled patients of cardiac rehabilitation participating in at least 75% of prescribed home-based CR sessions.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026