Resilience Enhancement Using Electronic Frailty Index-Directed Care Pathway
Recruiting now · Not applicable
Conditions studied: Cancer, Frail, Chemotherapy
In brief
The study purpose is to gain a better understanding of the needs of adults aged 65 and older while they are receiving chemotherapy by measuring their resilience and tailor care plans based on their individual needs.
Key facts
- Study ID
- NCT07175376
- Run by
- Wake Forest University Health Sciences
- People needed
- 32
- Starts
- 2026-03-16
- Expected to finish
- 2027-05-01
- Last updated by the study team
- 2026-07-02
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with cancer:
- Ability to understand and willingness to sign an IRB-approved informed consent
- Age ≥ 65 years at the time of enrollment.
- Planned to initiate an outpatient chemotherapy regimen (including myelosuppressive biologic/immune therapies) for cancer treatment (any type or stage), either as an initial therapy or as a new line of therapy, with curative or palliative intent.
- eFI pre-frail or frail status (available in EHR; defined as eFI > 0.10) within 30 days before enrollment.
- Ability to read and understand the English language
- Providers:
- Treating medical oncologist of at least one patient participant who enrolled on to the study and completed baseline assessment.
You may not qualify if…
- Patients:
- Documented physical or psychological comorbidity that would limit participant's ability to understand or comply with study procedures for the entire length of the study per the enrolling investigator.
- Chemotherapy planned at a facility outside the Atrium Health system.
- Currently receiving chemotherapy (defined as planned to continue an on-going treatment rather than starting a new regimen).
Where it is running
- Levine Cancer Institute — Charlotte, North Carolina, United States (enrolling)
- Atrium Health Wake Forest Baptist Comprehensive Cancer Center — Winston-Salem, North Carolina, United States (enrolling)
Full record on ClinicalTrials.gov
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