Cognitive Dysfunction and Breast Cancer Coping Strategies Impact on QOL
Status
Conditions
Treatments
Details and patient eligibility
About
The purpose of this study is to determine whether patients experience a better quality of life when they have received education about coping strategies for cognitive dysfunction.
Full description
Cancer treatment may consist of chemotherapy, radiation, hormone therapy, surgery or a combination of all disciplines. However, breast cancer therapies have at times demonstrated distressing effects in patients/survivors during and/or following treatment. One area that is found to cause distress for the breast cancer patient is changes in cognitive function.
Areas most commonly impacted by changes in cognitive function as a result of chemotherapy include executive functioning (including judgment, hindsight and foresight), processing speed or reaction time, working memory, and organizational skills.
Due to the limited amount of research involving quality of life as related to cognitive dysfunction, there is a clear need for additional investigation. Treatment typically focuses on the physical and psychosocial aspects of patients/survivors, however emphasis should also be placed on the impact of quality of life during treatment and survivorship due to the potential for far-reaching effects as previously discussed.
Oncology nurses may be instrumental in identifying patients with Cognitive Dysfunction. In doing so, the nurse may then communicate with the patient/survivor as to the impact of Cognitive Dysfunction on quality of life. The nurse can provide appropriate education and or additional support options.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Age >18years old
- Stage 0-IV breast cancer (excluding stage IV with metastasis to the brain)
- Life expectancy > 3 months
- Able to speak and read English fluently
- Self-reported cognitive difficulties that interfere with everyday activities
- Reported Memory/Cognitive changes on Distress Thermometer
- Able to provide written and informed consent
- Willing to complete FACT-Cog questionnaire
Exclusion criteria
- Current Cognitive Training, for example, use of brain training, physical therapy, occupational or speech therapy for the sole purpose of improving cognitive function
- Recent diagnosis of Major depression or other current psychiatric disorders and are not considered stable per a current care provider
- History of Dementia or Alzheimer's Disease
- History of Central Nervous System (CNS) radiation, intrathecal chemotherapy, or CNS involved surgery
- History of metastatic disease extending to the brain
- History of traumatic brain injury
- History of seizure disorder
- History of thyroid disorder (Subjects that are well managed without changes in thyroid medications or doses for at least 6 months may participate in study)
- Current use of illicit substances and or alcohol (including medical marijuana)
- Current sleep disturbance/disorder (Subjects that are well managed without changes in sleep medications or doses for at least 6 months may participate in study).
- Concurrent use of antidepressants for example, use of antidepressants for pain management or smoking cessation. (Subjects that are well managed without changes on antidepressant medications or doses for at least 6 months may participate in study).
Trial design
Primary purpose
Allocation
Interventional model
Masking
49 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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