Lung Cancer Clinical Trial

Healthy Directions After Lung Surgery Pilot

Summary

The objective of this proposal is to test the feasibility and acceptability of a lifestyle risk reduction intervention for patients with lung cancer receiving surgical treatment. This study will provide the preliminary data needed to conduct a larger randomized controlled trial that tests an innovative, multidisciplinary intervention that has the potential to transform the standard of care for patients receiving surgical treatment for lung cancer.

View Eligibility Criteria

Eligibility Criteria

Patient Inclusion Criteria:

> 21 years of age
English speaking
MD approval to participate in study
Meets one of the inclusions below:
1. a histological diagnosis of NSCLC undergoing potentially curative treatment
2. OR those undergoing surgical procedures for lung cancer (includes patients undergoing diagnostic testing or those presenting with lung nodules
3.OR patients who have had a surgical procedure for lung cancer within the last six months.
May invite a buddy to join study with them defined as a friend, partner, adult child or sibling

Buddy Inclusion Criteria:

≥ 21 years of age,
English speaking, who is invited by the subject to join as a support person (e.g., friend, partner, adult child or sibling)

Study is for people with:

Lung Cancer

Estimated Enrollment:

42

Study ID:

NCT02135211

Recruitment Status:

Completed

Sponsor:

Dana-Farber Cancer Institute

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There is 1 Location for this study

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Brigham & Woman's Hospital
Boston Massachusetts, 02115, United States
Dana Farber Cancer Institute
Boston Massachusetts, 02115, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Estimated Enrollment:

42

Study ID:

NCT02135211

Recruitment Status:

Completed

Sponsor:


Dana-Farber Cancer Institute

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