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Guided Imagery in the Perioperative Period in Gynecologic Oncology Patients
N/A
Waitlist Available
Led By Brandy Michaels, MD
Research Sponsored by University of Michigan
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
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.
Eligible Conditions
- Genitourinary Cancers
- Cervical Cancer
- Ovarian Cancer
- Ovarian Tumors
- Urogenital Neoplasms
- Fallopian Tube Cancer
- Uterine Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Guided ImageryExperimental Treatment1 Intervention
Guided Imagery With Audio Media
Group II: Routine Postoperative CareActive Control1 Intervention
Subjects will receive routine pre-operative, intra-operative, post-operative, chemotherapy, and radiation care as dictated by pathologic diagnosis.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Guided Imagery With Audio Media
2015
N/A
~130
Find a Location
Who is running the clinical trial?
University of MichiganLead Sponsor
1,863 Previous Clinical Trials
6,441,401 Total Patients Enrolled
Brandy Michaels, MDPrincipal InvestigatorUniversity of Michigan
J. Rebecca Liu, MDPrincipal InvestigatorUniversity of Michigan