A Study to Develop a Decision Aid for Patients Having Lung Screening

Overview

  • Study type

    Observational
  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • Site IRB
    • Rochester, Minnesota: 15-007773
    Sponsor Protocol Number: 15-007773

About this study

The purpose of this study is to collect data and then design a decision aid for patients who are having a lung screening.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Inclusion Criteria

  • Adults ≥ 18 years
  • Appointment for lung screening assessment

 

Exclusion Criteria

  • Major barriers to providing informed consent (i.e. dementia, severe hearing or visual impairment)

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Victor Montori, M.D.

Open for enrollment

Contact information:

Cara Fernandez

(507)266-1897

Fernandez.Cara@mayo.edu

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CLS-20206576

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