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Physical Activity and Neuropsychological Outcomes in a Cancer Population

Not Applicable
Completed
Conditions
Breast Cancer Survivors
Cognitive Dysfunction
Interventions
Behavioral: Exercise
Behavioral: Control
Registration Number
NCT02332876
Lead Sponsor
University of California, San Diego
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
87
Inclusion Criteria
  • 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.
Exclusion Criteria
  • 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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Exercise InterventionExerciseThis arm will receive a 12-week individually tailored phone and email-based exercise program.
Wellness Waitlist ControlControlThis arm will receive emails on the same schedule as the exercise arm, that cover a variety of health and wellness topics. At the end of the 12 weeks, participants will be able to start the exercise program.
Primary Outcome Measures
NameTimeMethod
National Institutes of Health Toolbox - Cognition Domain- Oral Symbol Digit TestBaseline to 12 weeks

Change in score on the NIH Toolbox Oral Symbol Digit test, an objective measure of processing speed, from baseline to 12 weeks. The Oral Symbol Digit test provides a raw score (possible range is 0-144). A higher score indicates better processing speed.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Moores UCSD Cancer Center

🇺🇸

La Jolla, California, United States

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