Lung Cancer Clinical Trial

Lung Heart Rate Variability

Summary

The purpose of this study is to examine the effects of heart-rate variability biofeedback training on lung cancer patients receiving definitive radiation therapy. The target population consists of non-small cell lung cancer (NSCLC) patients receiving 6 weeks of radiation therapy. The study will utilize the Physiolab GP8 heart rate variability and respiration system to collect data as well as several survey instruments to analyze quality of life measures. The goal is to show the HRV training can improve certain QOL measures like anxiety and sleep quality.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Participants must be older than 18 years of age
Both women and men of all ethnic background are eligible to participate in the study.
Must be diagnosed with non-small cell lung cancer and receiving 6 weeks of radiation therapy.
Must be available and willing to participate in 4, approximately 1 hour HRV biofeedback treatment sessions.
Signed informed consent

Exclusion Criteria:

Participant is younger than 18 or older than 70
Diagnosed with early stage NSCLC
Patients who are pregnant
Patients with cardiac arrhythmias
Patients with Pacemakers
Patients taking beta-blockers
Patients with any major mental illness, cognitive impairment
Incapable of giving informed consent

Study is for people with:

Lung Cancer

Study ID:

NCT03674450

Recruitment Status:

Withdrawn

Sponsor:

Abramson Cancer Center of the University of Pennsylvania

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There is 1 Location for this study

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Abramson Cancer Center of the University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Study ID:

NCT03674450

Recruitment Status:

Withdrawn

Sponsor:


Abramson Cancer Center of the University of Pennsylvania

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