Trials / Completed
CompletedNCT02444195
Guided Imagery in the Perioperative Period in Gynecologic Oncology Patients
Self-Administered Guided Imagery in the Perioperative Period to Reduce Postoperative Distress in Gynecologic Oncology Patients: A Randomized Control Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 130 (actual)
- Sponsor
- University of Michigan · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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
| Type | Name | Description |
|---|---|---|
| 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. |
Timeline
- Start date
- 2015-04-01
- Primary completion
- 2016-05-01
- Completion
- 2016-05-01
- First posted
- 2015-05-14
- Last updated
- 2017-03-20
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02444195. Inclusion in this directory is not an endorsement.