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Guided Imagery in the Perioperative Period in Gynecologic Oncology Patients

University of Michigan logo

University of Michigan

Status

Completed

Conditions

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

Treatments

Behavioral: Guided Imagery With Audio Media

Study type

Interventional

Funder types

Other

Identifiers

NCT02444195
HUM00095520

Details and patient eligibility

About

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.

Enrollment

130 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

130 participants in 2 patient groups

Guided Imagery
Experimental group
Description:
Guided Imagery With Audio Media
Treatment:
Behavioral: Guided Imagery With Audio Media
Routine Postoperative Care
No Intervention group
Description:
Subjects will receive routine pre-operative, intra-operative, post-operative, chemotherapy, and radiation care as dictated by pathologic diagnosis.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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