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NCT07227038

Living Well With Advanced Breast Cancer

Recruiting
Not specifiedAges 18+Observational
Ohio State University Comprehensive Cancer Center
~50 participants
Updated 2026-03-19 on ClinicalTrials.gov
What's tested:Non-Interventional Study

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Acceptability of current LWABC (Living Well with Advanced Breast Cancer) model
Measured over Up to study completion, up to 1 day
+2 more outcomes measured

Conditions

Advanced Breast Carcinoma
Anatomic Stage IV Breast Cancer AJCC v8
Metastatic Breast Carcinoma

Explore related trials

Breast Carcinoma

Where it's being run

1 sites across 1 states
Ohio1

Study leadership

  • Ashley P Davenport, MD · PRINCIPAL_INVESTIGATOR · Ohio State University Comprehensive Cancer Center

Who to contact

The Ohio State University Comprehensive Cancer Center
[email protected]
800-293-5066
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Eligibility criteria

Inclusion

\* 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

Patients who cannot provide own informed consent

What this trial measures

  • Acceptability of current LWABC (Living Well with Advanced Breast Cancer) modelUp 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 dataUp 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 cohortsUp 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.