Can Exercise Improve Cancer Associated Cognitive Dysfunction?

Breast Cancer Clinical Trial

— chemobrain  

Official title:

Can Exercise Improve Cancer Associated Cognitive Dysfunction?

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01296893
• Other study ID #: H10-02774
• Status: Completed
• Phase: Phase 2
• First received: February 9, 2011
• Last updated: June 5, 2016
• Start date: January 2011
• Est. completion date: June 2015

Study information

• Verified date: June 2016
• Source: University of British Columbia
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

Following chemotherapy, some breast cancer survivors report alterations in their ability to remember, concentrate, or think, which can have significant emotional, psychological, and economic impact on their lives. Survivors have also reported feeling frustrated by the response of the medical community, who either may not acknowledge their symptoms or have no treatment options to suggest. Exercise may be a promising treatment, as improvements in cognitive function with exercise have been demonstrated in older adults and other clinical populations.

The investigators will recruit women who have completed chemotherapy for breast cancer (within the past 2 years) and report cognitive changes. Women will be randomly assigned to either a 24-week aerobic exercise intervention or delayed exercise control (offered the same exercise program following the study). At the start and end of the study the investigators will measure: i) performance on four standard neuropsychological tests that measure working memory, learning, and problem solving; ii) a questionnaire on cognitive function and its impact on quality of life; iii) functional magnetic resonance imaging (fMRI) during two of the standard neuropsychological tests which provides information on how the brain is working during the tests.

To knowledge of the investigators this is the first study to examine the effect of an exercise intervention on cognitive function in breast cancer survivors. In addition, the use of fMRI imaging is a new way to approach this research question, and may be more sensitive to change than traditional measures of cognitive function.

Description:

Objective 1:

Conduct a randomized trial to test the effectiveness of a 24-week aerobic exercise intervention in adult, female breast cancer survivors with self-reported cognitive changes following chemotherapy.

The investigators will test the following hypotheses:

1. A) The exercise intervention will improve performance on neuropsychological tests of specific cognitive domains of executive function, namely i)selective attention and response inhibition, ii)processing speed and mental flexibility, and iii) verbal memory and learning in exercisers (EX; n=15) versus delayed exercise controls (CON; n=15).

B) The exercise intervention will reduce self-reported cognitive dysfunction and its impact of function and quality of life, in EX compared to CON, measured as a decreased score on the Functional Assessment Cancer Therapy-Cognition Scale (FACT-Cog).

Objective 2:

Conduct analyses on the effect of the intervention on brain activation patterns using functional magnetic resonance imaging (fMRI).

The investigators will test the following hypotheses:

2. A) At baseline, brain activation patterns will differ in breast cancer survivors reporting cognitive difficulties following chemotherapy compared to breast cancer survivors who have not received chemotherapy (who serve as breast cancer/no chemotherapy controls; not enrolled in the exercise intervention) during neuropsychological tests completed in the scanner.

B) The exercise intervention will result in a decrease in regions of cortical activation, particularly in regions that show higher activation in breast cancer survivors following chemotherapy, compared with no change in controls.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: June 2015
• Est. primary completion date: February 2014
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 40 Years to 75 Years

Eligibility

Inclusion Criteria:

• Women

• Completed chemotherapy within past 2 years

• completed for at least 3 months

• Self report cognitive dysfunction following chemotherapy

• Stage I-IIIA breast cancer

• Physically able to undertake moderate to vigorous physical activity program

Exclusion Criteria:

• Self report > 90min/week of moderate physical activity (last 6 months)

• Mini-mental status exam score < 23

• Co-morbid conditions that may alter cognitive testing results (i.e., a clinically diagnosed major depression, anxiety disorder, or other psychiatric condition, meeting DSM IV criteria)

• History of substance abuse

• Other neurological disorder (i.e., head injury, epilepsy, tumour, neurodegenerative disease)

• Ruled ineligible for MRI scanning (i.e., metal implants)

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Cognition Disorders

Intervention

Behavioral:
• Exercise
150 minutes/week of aerobic exercise at 60-70% of heart rate reserve (individualized based on baseline VO2 peak test). The intervention is 24 weeks with an exercise progression to reach the full exercise prescription by week 8. Participants are required to attend two 45 minute supervised sessions per week and complete two additional 30 minute sessions independently at home.

Locations

Country	Name	City	State
Canada	University of British Columbia	Vancouver	British Columbia

Sponsors (2)

Lead Sponsor	Collaborator
University of British Columbia	Canadian Breast Cancer Foundation

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Stroop Test	Tests response inhibition, measure number of correct vs incorrect responses	Change from baseline at 6 months	No
Secondary	FACT-Cog	Self-reported cognitive function and quality of life	Change from baseline at 6 months	No
Secondary	fMRI analyses	regions of interest analysis, whole brain patterns of change	Change from baseline at 6 months	No
Secondary	Graded exercise test		Change from baseline at 6 months	No
Secondary	Hopkins Verbal Learning Test	Verbal Learning, measure number of recalled and recognized words	Change from baseline at 6 months	No
Secondary	Trail Making A & B	Visual Conceptual and Visuomotor Tracking, measure time taken to complete	Change from baseline at 6 months	No