Breast Cancer Clinical Trial
Official title:
Guided Relaxation Training for the Reduction of Self-Reported Stress in Individuals With Newly Diagnosed Breast Cancer
The primary objectives of this study are to determine if the use of Guided Relaxation Training (GRT) during cancer treatment in individuals with newly diagnosed breast cancer increases their ability to cope as measured by the Coping Self-Efficacy Scale (CSES) and reduces their perceived stress as measured by the Perceived Stress Scale (PSS).
This is a study of self-reported stress in individuals with newly diagnosed breast cancer.
Subjects will be randomized to either the standard of care (SOC) arm or the intervention
arm. The principle investigators will be blinded to the arm assignment. The intervention
utilized will be six weekly on-site GRT sessions. In addition, subjects will be provided
with a CD utilizing a standardized GRT script and music for home use twice daily during the
study period. During the intervention period, they will also be provided with a diary and
required to keep a record of date and time of CD utilization at home. The subjects will also
be required to record their stress level before and after each of the two home sessions. The
sessions must be at least 4 hours apart.
The SOC arm will consist of an education session with the nurse or nurse practitioner and
supportive care / symptom management as needed. This group will also be required to keep a
daily diary in which they record their stress levels twice daily, at intervals separated by
at least 4 hours.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Supportive Care
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