Expired Study
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Ann Arbor, Michigan 48109


Purpose:

The purpose of this study is to evaluate the effectiveness of self-administered perioperative guided imagery to reduce perioperative distress in gynecologic oncology patients undergoing surgical management for a presumed cancer diagnosis.


Criteria:

Inclusion Criteria: - Undergoing surgical management for a suspected diagnosis of Gynecologic Malignancy (Endometrial, Ovarian, Vulvar, Vaginal, Primary Peritoneal, Fallopian Tube) - Age 18 or greater - Receiving care at University of Michigan Comprehensive Cancer Center Gynecologic Oncology Clinic or at St. Joseph Mercy Hospital, Alexander Cancer Care Center - Able to understand and read English - Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 - Patients must have working telephone, mobile or land line Exclusion Criteria: - Severe hearing impairment that limits the ability to use audio-based guided imagery modules - Current documented alcohol abuse or illicit drug substance abuse - Planned outpatient surgery - Patients currently participating in a meditation practice for more than 1 hour per week prior to preoperative visit.


NCT ID:

NCT02444195


Primary Contact:

Principal Investigator
Brandy Michaels, MD
University of Michigan


Backup Contact:

N/A


Location Contact:

Ann Arbor, Michigan 48109
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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