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Resilience Enhancement Using Electronic Frailty Index-Directed Care Pathway
RECRUITINGN/ASponsored by Wake Forest University Health Sciences
Actively Recruiting
PhaseN/A
SponsorWake Forest University Health Sciences
Started2026-03-16
Est. completion2027-01
Eligibility
Age65 Years+
Healthy vol.Accepted
Locations2 sites
View on ClinicalTrials.gov →
NCT07175376
Summary
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.
Eligibility
Age: 65 Years+Healthy volunteers accepted
Inclusion Criteria: 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 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) 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. Exclusion Criteria: 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
Conditions3
CancerChemotherapyFrail
Locations2 sites
Levine Cancer Institute
Atrium Health Wake Forest Baptist Comprehensive Cancer Center
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
PhaseN/A
SponsorWake Forest University Health Sciences
Started2026-03-16
Est. completion2027-01
Eligibility
Age65 Years+
Healthy vol.Accepted
Locations2 sites
View on ClinicalTrials.gov →
NCT07175376