Breast Cancer Clinical Trial
Development of a Clinical Trial Specific Question Prompt List
Summary
The purpose of this study is to develop a Question Prompt List (QPL) about clinical trials for cancer patients and find out what cancer patients and their caregivers think of the QPL. A QPL is a list of questions patients might want to ask their doctors during their appointments.
We will conduct three focus groups to talk about using QPL's as a new way to recruit patients like you to clinical trials. The three groups will be made of patients who have and have not participated in clinical trials, their caregivers and doctors. This study is also being done to learn about how the QPL affects the question asking behavior of patients during their appointments with doctors at Memorial SloanKettering Cancer Center (MSKCC).
Eligibility Criteria
Inclusion Criteria:
Population Segment 1 who have participated in a clinical trial
Diagnosis and treatment at MSKCC of lung, prostate or breast cancer
Completion of a Phase I, II, or III clinical trial at MSKCC
Ability to provide informed consent
Patient caregiver eligibility requirements will be:
Nomination by patient as the primary caregiver
Ability to provide informed consent
Population Segment 2 who have not participated in a clinical trial:
Diagnosis and treatment at MSKCC of lung, prostate or breast cancer or the primary patient caregiver
Ability to provide informed consent
Patient caregiver eligibility requirements will be:
Nomination by patient as the primary caregiver
Ability to provide informed consent
Population Segment 3 who are health care professionals:
A current health care professional at MSKCC
Current involvement in recruiting patients with lung, prostate or breast cancer to Phase I,II, or III clinical trials at MSKCC
Ability to provide informed consent
Exclusion Criteria:
Potential subjects will be considered ineligible for either/both phases of this study if they are:
Fewer than 18 years of age
Cognitively or physically impaired, rendering them incapable of providing informed consent to participate in the study
Population Segment 2 participants will be excluded if they have ever participated in a clinical trial.
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There is 1 Location for this study
New York New York, 10065, United States
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