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Chemotherapy-induced Cognitive and Brain Changes in Older Adults With Breast Cancer

Massachusetts General Hospital · NCT02290834

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 60+ · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
200
US sites recruiting
2
Study start
March 2015
Record last updated
July 16, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This research study evaluates the effect of chemotherapy on cognition (thinking) and the brain in people with breast cancer.

Being studied: Cognitive, functional and subjective assessments; MRI; PET Scan

Conditions: Impaired Cognition; Chemo-brain; Breast Cancer

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Breast cancer patients treated with chemotherapy- Group 1 (experimental group)
  • Participants must meet the following criteria on screening examination to be eligible to participate in the behavioral +/- imaging components of study
  • New diagnosis histologically confirmed invasive breast cancer
  • Treatment plan to include chemotherapy
  • Female subjects age ≥ 60 years.
  • Life expectancy ≥ 1 year
  • Karnofsky Performance Score (KPS) ≥ 80
  • Ability to understand and the willingness to sign a written informed consent document.
  • Non-treated breast cancer patient controls- Group 2 (control group)
  • Participants must meet the following criteria on screening examination to be eligible to participate in the behavioral +/- imaging components of study:
  • New diagnosis histologically confirmed invasive breast cancer
  • Treatment plan does not include chemotherapy
  • Age ≥ 60 years.
  • Life expectancy ≥ 1 year
  • Karnofsky Performance Score (KPS) ≥ 80
  • Ability to understand and the willingness to sign a written informed consent document.
  • Healthy control subjects- Group 3 (control group)
  • Participants must meet the following criteria on screening examination to be eligible to participate in the behavioral +/- imaging components of study:
  • Age ≥ 60 years.
  • Life expectancy ≥ 1 year
  • Karnofsky Performance Score (KPS) ≥ 80
  • Ability to understand and the willingness to sign a written informed consent document.
  • Participants with well-controlled vascular risk factors, such as treated hypertension, treated hyperlipidemia or well-controlled Type II diabetes (glucose levels \<250) may be included.
  • Serum Pregnancy Testing: STAT quantitative serum hCG pregnancy testing for all women of childbearing potential. Imaging will not start until and unless the test result returns negative.

Exclusion Criteria

  • Participants who exhibit any of the following conditions at screening will not be eligible for admission into the study:
  • Participants with clinical or radiographic evidence of metastatic CNS disease
  • Subjects with MMSE scores below 24
  • Active or history of major psychiatric disorders such as schizophrenia, schizoaffective disorder, major affective disorder in mid-life, or treatment with ECT (Mild depression that is well treated with stable dose of SSRI antidepressants may be allowed).
  • Substance abuse within the past 2 years
  • Huntington's disease, hydrocephalus or seizure disorder
  • In addition to exclusion criteria above, participants who exhibit any of the following conditions at screening will not be eligible for admission into imaging portion of the study:
  • Participants with contraindications to MRI (i.e., implanted metal including pacemakers, cerebral spinal fluid shunts, aneurysm clips, artificial heart valves, ear implants or metal/foreign objects in the eyes and those with a history of claustrophobia), injuries to the eyes with metal without X-ray documentation that metal was removed

Recruiting US locations

  • Massachusetts General Hospital

    Boston, MA 02114

    Site contact: Michael Parsons, PhD · 617-643-0282 · MWPARSONS@mgh.harvard.edu

  • Massachusetts General Hospital/North Shore Cancer Center

    Salem, MA 01970

    Site contact: Therese Mulvey, MD · (678) 882-6060 · TMMULVEY@PARTNERS.ORG

Study contacts (from the official record)

  • Michael W Parsons, PhD · 617-643-0282 · mwparsons@mgh.harvard.edu
All neurology studies in Massachusetts →
Chemotherapy-induced Cognitive and Brain Changes in Older Adults… (NCT02290834) | Bored Studies