Ovarian Cancer Clinical Trial
Official title:
Factors Associated With the Use of a High Volume Cancer Center by Black Women With Ovarian Cancer: A Qualitative Study
NCT number | NCT02928549 |
Other study ID # | 16-1378 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | September 22, 2016 |
Est. completion date | August 26, 2019 |
Verified date | August 2019 |
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 explore the experiences of Black women who receive care for ovarian cancer at Memorial Sloan Kettering Cancer Center, or "MSK" for short. The study consists of interviews with Black women who recently obtained some part of their ovarian cancer care at MSK.
Status | Completed |
Enrollment | 24 |
Est. completion date | August 26, 2019 |
Est. primary completion date | August 26, 2019 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Participant must have been diagnosed with ovarian, fallopian tube or primary peritoneal cancer and treated by an MSK physician. - Participants must be able to provide verbal informed consent. - Participants must be 18 years of age or older. - Participants must self-identify as Black/African American. - Participant must be able to understand and speak in English Exclusion Criteria: - Inability or refusal to identify race/ethnicity. - Presence or development of a physical, cognitive or psychiatric deficit resulting in an inability to provide meaningful informed consent or to understand the study or complete the interview. |
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 | accessing care | The study team will review and code the interview transcripts through a process of independent and collaborative thematic content analysis,[15-18] using ATLAS.ti (a qualitative data analysis software package) to facilitate the analysis process. | 1 year |
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