MedTrace Logo

Guided Imagery in the Perioperative Period in Gynecologic Oncology Patients

NCT02444195 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2017-03-20

No results posted yet for this study

Summary

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.

Conditions

  • Uterine Cervical Neoplasms
  • Uterine Neoplasms
  • Ovarian Neoplasms
  • Urogenital Neoplasms
  • Fallopian Tube Neoplasms

Interventions

BEHAVIORAL

Guided Imagery With Audio Media

Subjects assigned to the experimental arm will be asked to participate in meditation daily using the audio media provided for the 7 days prior to surgery, in the preoperative holding area, for the 7 days following surgery, and are encouraged to engage in affirmations module use at least weekly in the 6-8 week postoperative period.

Sponsors & Collaborators

Principal Investigators

  • Brandy Michaels, MD · University of Michigan

  • J. Rebecca Liu, MD · University of Michigan

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2016-05-01
Completion
2016-05-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02444195 on ClinicalTrials.gov