Emerging From the Haze™- Measuring the Impact of a Psycho-education Program on Perceived Cognition After Breast Cancer Treatment
Status: | Completed |
---|---|
Conditions: | Cancer, Cancer, Cognitive Studies, Cognitive Studies |
Therapuetic Areas: | Oncology, Psychiatry / Psychology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 11/3/2018 |
Start Date: | July 6, 2015 |
End Date: | May 23, 2018 |
Emerging From the Haze™-A Multi-center, Randomized Controlled Trial to Measure Impact of a Multi-dimensional Psycho-educational Program on Subjective Cognitive Complaints After Breast Cancer Treatment Using Virtual Technology
At Cedars-Sinai Medical Center, we have developed a novel curriculum for a 6-week
psycho-educationally-based, cognitive behavioral program to help patients with subjective
cognitive complaints after cancer treatment, titled Emerging from the Haze™ (Haze). Each
series meets once a week for 2 hours for 6 weeks. The leading neuropsychologist covers
material such as guided relaxation, behavioral strategies for automatic/negative thoughts,
compensatory strategies for attention and memory, executive functioning, pacing, and balance.
Each Haze series will be electronically delivered in a live format to our satellite site, The
University of Kansas.
psycho-educationally-based, cognitive behavioral program to help patients with subjective
cognitive complaints after cancer treatment, titled Emerging from the Haze™ (Haze). Each
series meets once a week for 2 hours for 6 weeks. The leading neuropsychologist covers
material such as guided relaxation, behavioral strategies for automatic/negative thoughts,
compensatory strategies for attention and memory, executive functioning, pacing, and balance.
Each Haze series will be electronically delivered in a live format to our satellite site, The
University of Kansas.
Inclusion Criteria:
- Completed treatment for stage 1-3 breast cancer at least two months but not more than
24 months prior to enrollment.
- Having received chemotherapy with or without radiation therapy
- Female, Age ≥18 years.
- FACT-Cog score less than 59 on the Perceived Cognitive Impairment subscale
- Eligible after 2 months of completing all their active cancer treatment with the
exception of long-term hormonal treatments or trastuzumab.
- Subjective complaint of cognitive concerns at time of enrollment
- Must be able to understand and communicate proficiently in English
- Ability to understand and the willingness to sign a written informed consent.
- Agree to complete study surveys
Exclusion Criteria:
- Patients who have significant personality disorders or unstable psychiatric disorders
(including active major depression, substance abuse, psychosis or bipolar disorder) as
assessed by the interviewing clinician
- Patients with known brain metastases, history of brain metastases or radiation to the
brain.
- Patients with a history of stroke or other pre-existing neurological condition that
may contribute to cognitive dysfunction.
- Non-English speakers
- Receiving treatment for another malignancy other than breast cancer
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, chronic anemia, uncontrolled hypothyroidism, symptomatic congestive heart
failure, unstable angina pectoris, uncontrolled cardiac arrhythmia, or psychiatric
illness/social situations that would limit compliance with study requirements.
We found this trial at
1
site
8700 Beverly Blvd # 8211
Los Angeles, California 90048
Los Angeles, California 90048
(1-800-233-2771)
Phone: 310-423-5162
Cedars Sinai Med Ctr Cedars-Sinai is known for providing the highest quality patient care. Our...
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