Memantine and Exercise to Improve Cognitive Function and Modulate Biological Pathways of Cognitive Decline During Chemotherapy in Breast Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUNC Lineberger Comprehensive Cancer Center

About this trial

This randomized, placebo-controlled trial aims to assess the feasibility, acceptability, and preliminary efficacy of memantine and the University of Carolina (UNC)'s Get Real \& Heel cancer exercise program (MEM+EX) in addressing cancer-related cognitive impairment (CRCI) and underlying CRCI biomarkers. Ninety stage I-III breast cancer patients during chemotherapy will be randomized into three groups: MEM+EX, memantine, or placebo. The study will evaluate recruitment, retention, adherence, acceptability, cognitive function, brain-derived neurotrophic factor (BDNF), inflammatory markers, and frailty at multiple time points.

Eligibility criteria

Qualifiers

Female

Age ≥ 18 years at the time of consent.

Stage I-III Breast Cancer

Recommended chemotherapy

Disqualifiers

Allergy to memantine

Previous chemotherapy (prior to the current regimen),

Severe cognitive impairment, defined by Blessed Orientation Memory Concentration Test Score ≥11

Myocardial infarction in the last 6 months

Trial design

Treatments tested in this trial

  • Memantine
  • Placebo medication
  • Exercise Intervention
  • Exercise Control

Treatment groups

90 Participants
are divided into 3 treatment groups

Sponsors and collaborators

UNC Lineberger Comprehensive Cancer Center

Lead sponsor

National Institute on Aging (NIA)

Collaborator