Connecting People With Cancer to Employment Support
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Details and patient eligibility
About
The goal of this clinical trial is to learn if a clinical workflow that screens adult patients with cancer for challenges at work and refers them to supportive resources is feasible, appropriate, and acceptable to patients and staff members in 2 cancer care settings. The main questions it aims to answer are:
Is the clinical workflow feasible and acceptable to participants? Are study procedures feasible and acceptable to participants?
Patient participants will complete 2 surveys: 1 at the time of enrollment and 1 six months later.
Full description
Investigators will conduct a prospective single-arm study at 2 sites to pilot and iteratively adapt a clinical workflow intervention, implementation strategies, and associated study procedures. Investigators will implement the clinical workflow intervention across each study site, then recruit consecutive patients (n=50) to complete patient-reported measures at 2 time points (T1: enrollment; T2: 6-month follow-up. Investigators will recruit staff members (n=20) to complete survey measures at 2 time points (T1: beginning of pilot study period; T2: end of pilot study period).
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Eligible Patients:
- visiting a participating medical or radiation oncology clinic for new diagnosis, treatment, or follow-up of any type of cancer;
- employed at the time of cancer diagnosis;
- age 18 or older;
- able to give full informed consent;
- able to communicate in English or Spanish.
Eligible Staff:
- age 18 or older;
- employed at one of the participating clinical sites.
Trial design
Primary purpose
Allocation
Interventional model
Masking
70 participants in 1 patient group
Trial contacts and locations
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Central trial contact
Rachel C. Forcino, PhD, MSc
Data sourced from clinicaltrials.gov
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