Thyroid Cancer Clinical Trial
Official title:
Treatment Decision-Making Among Patients Diagnosed With Papillary Microcarcinoma and Their Significant Others
Verified date | June 2017 |
Source | Memorial Sloan Kettering Cancer Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to understand more about why some patients choose to have surgery to treat their papillary microcarcinoma (PMC) and others choose to have their papillary microcarcinoma (PMC) regularly watched by their doctor to see if and when they may need surgery (referred to as "active surveillance"). The investigators also hope learn more about what patients and their family members worry about or feel they will gain from surgery or active surveillance.
Status | Completed |
Enrollment | 21 |
Est. completion date | June 2017 |
Est. primary completion date | June 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Thyroid cancer patient eligibility will include: - Thyroid cancer patients who have been diagnosed with papillary microcarcinoma (or subcentimeter thyroid lesions with fine needle aspiration biopsy suspicious for papillary or follicular thyroid cancer) within the prior 6-12 months as per EMR path report and clinician assessment; - Presented with the option of treating their papillary microcarcinomas with either surgery or active surveillance as per treating physician; - English-fluent; - 18 years of age or older; Patient-designated significant other eligibility will include: - Nomination by patient as individual who assisted patient in decision-making regarding how to treat thyroid papillary microcarcinoma; - English-fluent; - 18 years of age or older; Exclusion Criteria: Thyroid cancer patient exclusion criteria will include: - Thyroid cancer patients with known loco-regional or distant metastases prior to initial surgical intervention as per path report. |
Country | Name | City | State |
---|---|---|---|
United States | Memorial Sloan Kettering Cancer Center | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Memorial Sloan Kettering Cancer Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To explore patients' and families' perceived risks and benefits of active surveillance and surgery within the context of papillary microcarcinoma. | We'll conduct focus groups & individual interviews with 2 population segments established by the method of Krueger & Casey & Morgan. The population segments will be thyroid cancer patients who have had surg or have scheduled surg, & any pt-designated significant others who assisted pts with tx decision-making & thyroid cancer pts who chose to not have immediate surg, whether they are either postponing their tx decision until a later date, or have committed to active surveillance rather than surg, & any pt-designated significant others who assisted these patients with tx decision-making. | 5 years | |
Secondary | To examine the factors in patients' and families' decision making about the treatment of papillary microcarcinoma. | We'll conduct focus groups & individual interviews with 2 population segments established by the method of Krueger & Casey & Morgan. The population segments will be thyroid cancer pts who have had surg or have scheduled surg, & any pt-designated significant others who assisted patients with tx decision-making & thyroid cancer pts who chose to not have immediate surg, whether they are either postponing their tx decision until a later date, or have committed to active surveillance rather than surg, & any patient-designated significant others who assisted these pts with tx decision-making. | 5 years |
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