New tool aims to predict chemo risks for seniors
NCT ID NCT00477958
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a geriatric assessment tool—looking at thinking, memory, daily activities, and emotional well-being—can predict serious side effects from chemotherapy in older adults with cancer. Over 1,000 patients completed questionnaires and cognitive tests before and after treatment. The goal is to help doctors tailor cancer care for seniors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors better predict which older patients are at risk for serious side effects from chemotherapy, leading to more personalized treatment plans.
- What could go wrong
- This is an observational study, not a treatment trial. The assessment tool may not accurately predict toxicity, and results may not apply to all older 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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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1,062 people
The number who actually took part.
- Started
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Dec 2006
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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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.
- Ages
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65 to 120 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
DISEASE CHARACTERISTICS: * Pathologically confirmed cancer * Receiving chemotherapy for either adjuvant treatment or metastatic disease prior to beginning a new chemotherapy regimen PATIENT CHARACTERISTICS: * Must be able to understand English PRIOR CONCURRENT THERAPY: * See Disease Characteristics * No prior enrollment in this trial * No concurrent enrollment on a phase I clinical trial
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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.
Contacts and locations
Locations
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Case Comprehensive Cancer Center
Cleveland, Ohio, 44106-5065, United States
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Chao Family Comprehensive Cancer Center at University of California Irvine Medical Center
Orange, California, 92868, United States
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City of Hope Medical Center
Duarte, California, 91010-3000, United States
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James P. Wilmot Cancer Center at University of Rochester Medical Center
Rochester, New York, 14642, United States
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Memorial Sloan-Kettering Cancer Center
New York, New York, 10065, United States
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Tower Cancer Research Foundation
Beverly Hills, California, 90211, United States
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Wake Forest University Comprehensive Cancer Center
Winston-Salem, North Carolina, 27157-1096, United States
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Yale Cancer Center
New Haven, Connecticut, 06520-8028, United States
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