Expired Study
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Los Angeles, California 90048


Purpose:

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.


Criteria:

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.


NCT ID:

NCT02360917


Primary Contact:

Principal Investigator
Jamie Myers, PhD, RN AOCNSP
University of Kansas


Backup Contact:

N/A


Location Contact:

Los Angeles, California 90048
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 25, 2018

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