Computer-Based Training in Patients With Post-Chemotherapy Cognitive Impairment

NCT ID: NCT00387062

Last Updated: 2008-06-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-10-31

Study Completion Date

2008-06-30

Brief Summary

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The investigators hypothesize that continuous active interaction with environments that are demanding to sensory, cognitive, and motor systems, together with imbedded rewards for successful performance, will help improve memory and cognitive functioning in patients suffering from "chemobrain".

Detailed Description

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Breast cancer is the most common malignancy in women in the United States, with an estimated 211,240 new cases of invasive breast cancer diagnosed among women, and 1,700 diagnosed in men, in 2005. While cure rates have improved significantly, chemotherapy for breast cancer is associated with a number of negative side effects. One of which is a deficit in cognitive function, a condition commonly referred to as "chemobrain". While the debate about cognitive decline being a result of chemotherapy is still ongoing, there is clear evidence of cognitive decline in women with breast cancer post-chemotherapy. Cognitive decline is often reported to affect memory, attention, executive functioning and information processing speed.

Studies suggest that incidence of "chemobrain" ranges from 17% - 75% in women who have undergone chemotherapy.This cognitive impairment affects quality of life by impacting patients' ability to concentrate, make decisions and to fulfill family, career, and community responsibilities.

Although there is uncertainty about the mechanisms that can lead to this cognitive decline, there is a pressing need to identify interventions that will alleviate its symptoms and help breast cancer survivors recover their cognitive functioning and resume their roles and activities at the pre-cancer level.

Brain plasticity refers to the brain's capacity for physical and functional change; it is this capacity that explains how experience induces learning throughout life. On the basis of a growing body of literature in the fields of psychophysics, neurology, neuropsychology, and brain plasticity, we hypothesize that the brain processing machinery can be refined, elaborated, and strengthened through rigorous training and learning. The purpose of this study is to investigate if such training can improve cognitive functioning.

We hypothesize that continuous active interaction with environments that are demanding to sensory, cognitive, and motor systems, together with imbedded rewards for successful performance will help improve memory and cognitive functioning in patients suffering from "chemobrain".

Conditions

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Breast Cancer Cognitive Symptoms Memory Disorders

Keywords

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Breast Cancer Cognitive Impairment Chemofog Chemobrain Post-chemotherapy cognitive impairment

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Interventions

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Computer-based Cognitive Training

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Age 21 or older at the time of consent.
* Diagnosis of invasive breast cancer or recurrence warranting treatment with chemotherapeutic agents in the past 5 years.
* Cognitive decline, as reported by the patient, friends, or family.
* Fluent English speaker.
* Willing and able to commit to the 6-month time requirement of the entire study period.
* Willing to provide informed consent
* Willing to participate in training of the program.
* Agrees to weekly contact

Exclusion Criteria

* Severe hearing impairments that would:

* limit the ability to receive instructions and support; and
* hinder performance on the computer training program.
* Self-report of untreated Axis I or II disorders (with the exception of depression, anxiety disorders, and panic disorders).
* Self-report of current diagnosis or history of major neurological illness including, but not limited to:

* Alzheimer's disease
* Parkinson's disease
* Multiple sclerosis
* Amyotrophic lateral sclerosis
* History of a stroke, transient ischemic attack (TIA) or traumatic brain injury within the past year; or lifetime history of stroke, TIA, or traumatic brain injury that has left residual expressive or receptive language problems.
* Self-report of fibromyalgia or symptoms of tremor severe enough to prevent the use of a computer mouse or other pointing device.
* Unwillingness to complete the required assessments.
* Patient is not capable of giving informed consent or unable to comprehend and/or follow instructions.
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Posit Science Corporation

INDUSTRY

Sponsor Role lead

Principal Investigators

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Henry W Mahncke, PhD

Role: PRINCIPAL_INVESTIGATOR

Posit Science Corporation

Locations

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Posit Science Corporation

San Francisco, California, United States

Site Status

Countries

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United States

References

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Other Identifiers

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OUT-113-2005; 06140-01

Identifier Type: -

Identifier Source: org_study_id