Quality of Life Intervention to Inform Patient Decision-Making in Early-Stage Lung Cancer

Description

This clinical trial studies the effect of a quality of life intervention on decision-making in patients with early-stage lung cancer who are undergoing standard of care surgery or stereotactic body radiation therapy (SBRT). Providing quality of life outcome data to patients deciding between surgery and SBRT may help decrease decision regret and increase patient satisfaction with their care.

Conditions

Lung Non-Small Cell Carcinoma, Stage I Lung Cancer AJCC v8, Stage IA1 Lung Cancer AJCC v8, Stage IA2 Lung Cancer AJCC v8, Stage IA3 Lung Cancer AJCC v8, Stage IB Lung Cancer AJCC v8, Stage II Lung Cancer AJCC v8, Stage IIA Lung Cancer AJCC v8, Stage IIB Lung Cancer AJCC v8

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Study Overview

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Study Details

Study overview

This clinical trial studies the effect of a quality of life intervention on decision-making in patients with early-stage lung cancer who are undergoing standard of care surgery or stereotactic body radiation therapy (SBRT). Providing quality of life outcome data to patients deciding between surgery and SBRT may help decrease decision regret and increase patient satisfaction with their care.

Utilizing Patient Reported Quality of Life to Inform Patient Decision Making in Early-Stage Lung Cancer

Quality of Life Intervention to Inform Patient Decision-Making in Early-Stage Lung Cancer

Condition
Lung Non-Small Cell Carcinoma
Intervention / Treatment

-

Contacts and Locations

Buffalo

Roswell Park Cancer Institute, Buffalo, New York, United States, 14263

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Age \>= 18 years
  • * Radiographic stage I-II non-small cell lung cancer (NSCLC)
  • * Eligible for both surgery and SBRT
  • * Able to provide informed consent in English
  • * Have verbal fluency in English
  • * Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure
  • * Radiographic stage III-IV NSCLC
  • * Eligible for either only surgery or SBRT, but not both
  • * Eligible for palliative-intent treatments or supportive care only.
  • * Pregnant female participants.
  • * Unwilling or unable to follow protocol requirements
  • * Any condition which in the investigator's opinion deems the participant an unsuitable candidate
  • * Cognitively impaired adults/adults with impaired decision-making capacity
  • * Individuals who are not yet adults (infants, children, teenagers)
  • * Prisoners

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Roswell Park Cancer Institute,

Anurag K Singh, PRINCIPAL_INVESTIGATOR, Roswell Park Cancer Institute

Study Record Dates

2025-01-15