ClinicalTrials.Veeva

Menu

Aging and Frailty Study

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Completed

Conditions

Aging
Frailty
Effects of Chemotherapy

Treatments

Other: Geriatric Assessments and Frailty Indices

Study type

Observational

Funder types

Other

Identifiers

NCT05268991
IRB00080711
WFBCCC 04721 (Other Identifier)

Details and patient eligibility

About

The purpose of this research study is to compare methods to help personalize the prediction of chemotherapy side effects for older adults and to evaluate whether chemotherapy causes changes in the body that are associated with aging.

Full description

Primary Objective: Describe mean and variation of the electronic frailty index-cancer, geriatric measures, patient reported outcomes, and biomarkers of aging of chemotherapy, and their change.

Enrollment

25 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 65 years and older
  • Planned to initiate a new chemotherapy regimen
  • Solid tumor malignancy of any stage or lymphoma
  • Any performance status
  • Ability to understand and the willingness to sign an IRB-approved informed consent document (either directly or via a legally authorized representative).
  • Life expectancy of ≥3 months

Exclusion criteria

  • Initiating biologic, endocrine or immunotherapy only.
  • Hematologic malignancy other than lymphoma.
  • Concurrent radiation therapy.
  • Planned inpatient chemotherapy.

Trial design

25 participants in 1 patient group

AGE Participants
Description:
Participants aged 65 and older with diagnosis of solid tumor malignancy or lymphoma and planned to start a new chemotherapy regimen in the outpatient setting
Treatment:
Other: Geriatric Assessments and Frailty Indices

Trial contacts and locations

1

Loading...

Central trial contact

Study Coordinator

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems