New tool aims to cut chemo toxicity for seniors with cancer
NCT ID NCT06870617
First seen Jun 27, 2026 · Last updated Aug 07, 2026 · Updated 2 times
Summary
This study tests a practical geriatric assessment (PGA) for adults aged 70+ with advanced cancer. The PGA is a questionnaire completed before a doctor visit, and results are shared with the care team to help guide chemotherapy dosing. Researchers will also track step counts with a FitBit and measure body composition from CT scans to see if these factors relate to side effects. The goal is to make geriatric assessments easier to use and reduce treatment-related toxicity.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Practical Geriatric Assessment (PGA) questionnaire and FitBit step monitoring
- What this could lead to
- If successful, this could make geriatric assessments easier to use in clinics, helping doctors tailor chemotherapy to reduce side effects in older patients.
- What could go wrong
- This is an early implementation study, not a large trial. The assessment may not change outcomes, and results may not apply to all older cancer patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jul 2025
- Expected to finish
-
Oct 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Eligible participants will be 70 years or older, have a diagnosis of advanced or metastatic solid malignancy, and be starting a new line of palliative-intent systemic therapy, where the expected prevalence of grade 3 toxicity exceeds 50 percent.
- Ages
-
70 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
For PGA Implementation Cohort, patients must meet the following criteria: 1. Age greater than or equal to 70 years. 2. Diagnosis of advanced or metastatic solid malignancy 3. Initiating a new line of palliative-intent systemic therapy with a prevalence of grade 3 toxicity exceeding 50%. For Correlative Analysis Cohort, patients must additionally meet the following criteria: 1. Must read and speak English and be able to fill out surveys 2. Ability to walk independently or with the use of an assistive device (e.g., walker, cane) 3. Consents to participate in correlative analysis cohort with Fitbit monitoring, body composition analysis, and self-report surveys 4. Have a smartphone able to operate with the Fitbit For PGA Implementation Cohort, there are no specific exclusion criteria other than not meeting inclusion criteria. For Correlative Analysis Cohort, patients will be excluded if meeting any of the following criteria: 1. Unable to effectively read and speak English 2. Reliance on a wheelchair, ECOG of 3 or above, clinically bedbound, or unable to walk without assistance every day for the past 7 days (ECOG 3 is confined to bed or chair for more than 50% of waking hours) 3. Concurrent enrollment in a therapeutic clinical trial (as clinical trials often have a substantial symptom-reporting structure). Non-therapeutic clinical trial enrollment is permitted 4. Lack of clinician consent to approach patient
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Advanced cancer are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
3 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Lancaster General Hospital
NOT_YET_RECRUITINGLancaster, Pennsylvania, 17602, United States
-
Penn Medicine Princeton Medical Center
RECRUITINGPrinceton, New Jersey, 08540, United States
-
Pennsylvania Hospital
RECRUITINGPhiladelphia, Pennsylvania, 19107, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a video game teach cancer patients to tame their pain?
- Real-World melanoma care under the microscope
- Can a single psychedelic dose ease despair in advanced cancer?
- Can a detailed health check predict who thrives after a stem cell transplant?
- Can tracking symptoms improve care for children with advanced cancer?
- Can a new pill boost Immunotherapy's power against advanced tumors?