Physical Activity and Neuropsychological Outcomes in a Cancer Population

Completed · Not applicable

Conditions studied: Cognitive Dysfunction, Breast Cancer Survivors

In brief

Many cancer survivors experience treatment-related impairments in mental abilities such as memory, attention, and concentration (known as cognition). Research indicates that physical activity can improve cognition in healthy adults; however, little is known about whether physical activity can improve cognition among cancer survivors. This study will test whether a physical activity intervention results in improvements in cognition among breast cancer survivors, which may lead to interventions to improve cognition.

Key facts

Study ID

NCT02332876

Run by

University of California, San Diego

People needed

87

Starts

2014-08-01

Expected to finish

2016-07-01

Last updated by the study team

2018-07-11

Who can join

Age: 21 and older, up to 85. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• breast cancer survivors; diagnosed at stage 1, 2, or 3 less than 5 years ago -
• not scheduled for or currently undergoing chemotherapy; sedentary, defined as engaging in less than 60 minutes of moderate to vigorous physical activity each week
• accessible geographically and by telephone
• have access to the internet
• endorse experience difficulties with thinking abilities
• in addition, participants on adjuvant therapy (e.g., tamoxifen or aromatase inhibitors) must be able and willing to remain on that treatment for the 3-month intervention period to prevent confounding of biomarker concentrations by treatment.

You may not qualify if…

• history of coronary heart disease, diabetes, stroke, orthopedic conditions that limit mobility, or any other serious medical condition that could make it potentially unsafe to be in an unsupervised physical activity intervention
• other primary or recurrent invasive cancer within the last 10 years (other than nonmelanoma skin cancer or carcinoma of the cervix in situ)
• unable to commit to a 3-month intervention schedule; any condition that, in the investigators' judgment, would contraindicate increased physical activity or otherwise interfere with participation in the trial
• unable to provide a blood sample at the baseline measurement visit
• unable to speak and read English.

Where it is running

• Moores UCSD Cancer Center — La Jolla, California, United States

Full record on ClinicalTrials.gov

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