Physical Activity and Inactivity in Lung Cancer Survivors

Completed

• Conditions: Lung Cancer Survivors

• Registration Number: NCT00582348
• Lead Sponsor: Memorial Sloan Kettering Cancer Center

Brief Summary

The purpose of this study is to learn how often lung cancer survivors exercise. We also want to learn what helps people to be active or prevents them from being active. Learning this will help us to expand services for lung cancer survivors.

Detailed Description

Despite the potential benefits of physical activity, particularly for cancer survivors with comorbid pulmonary and cardiac conditions, no previous research has examined the physical activity levels of lung cancer survivors, an underrepresented subpopulation in cancer survivorship research. We address this research gap in the current study, in which a random sample of 200 lung cancer survivors will complete a comprehensive telephone interview or use self-report to complete a questionnaire focusing on physical activity, related covariates, and preferences regarding physical activity counseling and interventions. We estimate the total time for the completion of the interview or self-report questionnaire to be 45-60 minutes. This study will be conducted with survivors of primary lung cancer who are from 1 to 5 years posttreatment and were treated at Memorial Sloan-Kettering Cancer Center (MSKCC).

Study Timeline

• Study Start: 2005-09
• Study First Submitted: 2007-12-21
• Study First Submitted QC: 2007-12-21
• Study First Posted: 2007-12-28
• Status Verified: 2020-02
• Primary Completion: 2020-02-10
• Study Completion: 2020-02-10
• Last Update Submitted: 2020-02-11
• Last Update Posted: 2020-02-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 188

Inclusion Criteria

• Diagnosis of primary Stage IA or IB NSCLC;
• Underwent surgical resection for NSCLC at MSKCC;
• From 1 to 5 years post-treatment for NSCLC prior to study recruitment;
• No evidence of disease (NED) at the time of recruitment;
• Can be reached by telephone;
• Able to provide informed consent.

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Exclusion Criteria

• Undergoing active antineoplastic treatment;
• Major psychopathology or cognitive impairment likely in the judgment of the investigator to interfere with participation and compliance with the protocol.

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcomes of this study are physical activity levels and preferences regarding physical activity counseling and interventions	45-60 minutes

Trial Locations

Locations (1)

Memorial Sloan-Kettering Cancer Center; 🇺🇸 New York, New York, United States