Living Well With Advanced Breast Cancer
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- Acceptability of current LWABC (Living Well with Advanced Breast Cancer) model
Study Overview
Brief Summary
This study evaluates the use of supportive care in patients with advanced breast cancer to better understand what has helped them, what has been hard, and what kind of help they still need.
Detailed Description
PRIMARY OBJECTIVES:
I. Assess acceptability of current LWABC model. II. Conduct a comprehensive review of participants' medical history, treatment records, and demographic data.
III. Explore differences in survivorship care engagement across four distinct cohorts.
OUTLINE: This is an observational study.
Participants complete a survey and a semi-structured interview on study.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •* COHORT 1:
- •Diagnosis of stage 4 metastatic breast cancer within the past 5 years
- •Never been referred to the LWABC
- •Adults age ≥ 18 years
- •COHORT 2:
- •Diagnosis of stage 4 metastatic breast cancer within the past 5 years
- •Have cancelled an appointment with the LWABC
- •Adults age ≥ 18 years
- •COHORT 3:
- •Been seen in the Medical Oncology Clinic at Stephanie Spielman Comprehensive Breast Center (SSCBC) within the past 5 years
- •Completed an appointment with the LWABC
- •Adults age ≥ 18 years
- •COHORT 4:
- •Caregivers for ABC patients
- •Adults age ≥ 18 years
Exclusion Criteria
- •Patients who cannot provide own informed consent
Arms & Interventions
Observational
Patients complete a survey and a semi-structured interview on study.
Intervention: Non-Interventional Study (Other)
Outcomes
Primary Outcomes
Acceptability of current LWABC (Living Well with Advanced Breast Cancer) model
Time Frame: Up to study completion, up to 1 day
Will utilize a thematic inductive analysis approach to compare and contrast themes across cohorts. Survey items will be summarized by cohort. Means, standard deviations, medians and ranges will be calculated for continuous variables and frequency, percents and 95% confidence intervals will be calculated for categorical variables.
Participant medical history, treatment records, and demographic data
Time Frame: Up to study completion, up to 1 day
Will utilize a thematic inductive analysis approach to compare and contrast themes across cohorts. Survey items including demographic information and disease characteristics will be summarized by cohort. Means, standard deviations, medians and ranges will be calculated for continuous variables and frequency, percents and 95% confidence intervals will be calculated for categorical variables.
Differences in survivorship care engagement across four distinct cohorts
Time Frame: Up to study completion, up to 1 day
Will utilize a thematic inductive analysis approach to compare and contrast themes across cohorts. Themes will be compared across each cohort to identify survivorship care needs that will be translated into intervention components for the ABC survivorship program. Survey items will be summarized by cohort. Means, standard deviations, medians and ranges will be calculated for continuous variables and frequency, percents and 95% confidence intervals will be calculated for categorical variables.
Secondary Outcomes
No secondary outcomes reported
Investigators
Ashley Davenport
Principal Investigator
Ohio State University Comprehensive Cancer Center