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Rehabilitation of Cognitive Changes in Breast Cancer Survivors

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
MARTELL FOUNDATION
Information provided by (Responsible Party):
Memorial Sloan-Kettering Cancer Center
ClinicalTrials.gov Identifier:
NCT01182506
First received: August 12, 2010
Last updated: February 18, 2014
Last verified: February 2014

August 12, 2010
February 18, 2014
August 2010
August 2014   (final data collection date for primary outcome measure)
Determine the efficacy of working memory training [ Time Frame: 2 years ] [ Designated as safety issue: No ]
in breast cancer survivors based on improved performance on neuropsychological tests of working memory.
Same as current
Complete list of historical versions of study NCT01182506 on ClinicalTrials.gov Archive Site
  • Test whether or not working memory training in breast cancer survivors is associated with greater gains in the software's "Improvement Index". [ Time Frame: 2 years ] [ Designated as safety issue: No ]
  • Investigate whether breast cancer survivors perceive functional improvement following working memory training. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Rehabilitation of Cognitive Changes in Breast Cancer Survivors
Rehabilitation of Cognitive Changes in Breast Cancer Survivors

The purpose of this study is to test a memory training program for breast cancer survivors who have problems with memory after receiving chemotherapy. Since breast cancer survivors have been reported to have trouble with their memory, a program to help these problems is important. Studies have shown that a 5-week software training program improved memory in pediatric cancer survivors and other disorders like stroke, but it has not been tested for breast cancer survivors. This study will see if breast cancer survivors can improve their memory and attention problems by using either one of two software versions of the program. One version is called Cogmed Working Memory Training, and the other is a comparison version of the software that has the same exercises but is less difficult. People who decide to participate in the study will be randomly given one of the two versions.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Supportive Care
Breast Cancer
Behavioral: Cogmed Working Memory Training Program

Women will be randomized to one of two 5-week rehabilitation software training programs that train working memory called Cogmed Working Memory Training Program.

The training software will be provided to each participant. For each group, training occurs for 30 minutes a day, 5 days a week for 5 weeks. As part of the set-up, training data is uploaded to the internet at a minimum of every 3 days. This function allows the "coach" (in this case, the PI and RSA) to review the training. A weekly "coach" phone call is made to review the training results, answer questions, troubleshoot, and motivate the participant. Participants can load the software onto multiple computers to provide flexibility for them to do training at home, after work, when they are away from home.

  • Experimental: Breast cancer survivors
    Participants from both groups will be asked to complete two follow up neurocognitive assessments face to face at MSKCC. The first will be completed within 1-4 weeks after completing the memory training and the second will take place 3-4 months after completing the memory training. Collateral sources will be contacted at these same points to complete their brief assessments as well to test for maintenance of the treatment effect.
    Intervention: Behavioral: Cogmed Working Memory Training Program
  • Experimental: Collateral source
    Participants from both groups will be asked to complete two follow up neurocognitive assessments face to face at MSKCC. The first will be completed within 1-4 weeks after completing the memory training and the second will take place 3-4 months after completing the memory training. Collateral sources will be contacted at these same points to complete their brief assessments as well to test for maintenance of the treatment effect.
    Intervention: Behavioral: Cogmed Working Memory Training Program
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
60
August 2014
August 2014   (final data collection date for primary outcome measure)

Note: Any participant who reports tics can be included, however participants will be told tics may increase during the training period.

Inclusion Criteria:

Patients

  • Female breast cancer survivors who have received adjuvant chemotherapy 1-10 years from the time of recruitment either at MSKCC or elsewhere
  • Stage I, II, III breast cancer as noted in pathology reports or by clinician judgement.
  • No evidence of disease at time of screening
  • Age range 18 years old through <70 years old
  • Must be able speak, read and write English well enough to complete written and verbal assessments and neurocognitive tests. The software was developed and validated in English and are not currently available in other languages. Translation of questionnaires into other languages would require reestablishing the reliability and validity of these measures.
  • Must demonstrate cognitive deficiency, which is defined as 1.0 standard deviations below normative data on at least one of the pre-screen phone assessments (WAIS-III Digit Span, Symbol Digit Modalities Test, Controlled Oral Word Association Test, Rey Auditory Verbal Learning Test) or must have 1.0 standard deviations difference from the pre-morbid estimate of cognitive functioning, Wide Range Achievement Test 4: Reading subtest, and one of the pre-screen phone assessment measures.
  • Must have basic computer skills such as able to turn on a computer, open the program, login, and use a mouse.
  • Participants must have the ability to upload their data via the internet. A study laptop can be loaned out to participants who do not have a computer or the appropriate operating systems.

Collateral Participant (if such person is available to the participant, not a requirement of the study) Family member or friend (i.e., collateral) identified by a patient who has at least weekly face to face contact with the patient

  • Collateral person is at least 18 years of age
  • Family member or friend has adequate English fluency for completion of data collection. The surveys were designed and validated in English and are not currently available in other languages. Translation of questionnaires into other languages would require reestablishing the reliability and validity of these measures.
  • Able to provide informed consent

Exclusion Criteria:

Patients

  • History of neurological disorder with cognitive symptoms (e.g., Alzheimer's disease, Parkinson's disease, multiple sclerosis, seizure disorder) as per self report or as documented in the electronic medical record.
  • History of mental retardation, learning disorder bipolar disorder, schizophrenia, substance use disorder(s), or uncontrolled depression as per self report or as documented in the medical record.
  • History of Traumatic Brain Injury with > or = to 30 minutes loss of consciousness or cognitive sequelae as per self report or as documented in the medical record.
  • History of Stroke as per self report or as documented in the medical record.
  • Prior history or secondary diagnosis of other cancers except for basal cell carcinoma or melanoma treated with surgery only
  • History of multiple courses of chemotherapy.
  • Evidence of recurrence at time of screening
  • A hearing or visual deficit that impairs the ability to use the software.
  • Significant cognitive or psychiatric disturbance sufficient, in the investigator's judgment, to preclude providing informed consent.
  • Males will be excluded as only a minority of men gets breast cancer. Thus, there would not be enough men to have equivalent groups to statistically control for possible gender effects.
Female
18 Years to 69 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01182506
10-105
Not Provided
Memorial Sloan-Kettering Cancer Center
Memorial Sloan-Kettering Cancer Center
MARTELL FOUNDATION
Principal Investigator: Elizabeth Ryan, PhD Memorial Sloan-Kettering Cancer Center
Memorial Sloan-Kettering Cancer Center
February 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP