Clinical Trials Directory

Trials / Terminated

TerminatedNCT01284075

The Effect of Guided Imagery and Music Therapy on Post-Operative Recovery After Gynecological Oncology Surgery

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
University of Minnesota · Academic / Other
Sex
Female
Age
19 Years
Healthy volunteers
Not accepted

Summary

This pilot study will be a prospective, randomized trial which will take place at the University of Minnesota Medical Center (UMMC). Eligible patients will be identified at the time of their first clinic visit. If selected to be involved in the study, the patients will be randomized to one of three different groups: a Guided Imagery and Music therapy group (GIMT) or one of two control groups.

Detailed description

The GIMT group will undergo a standardized regimen of peri-operative guided imagery and music therapy guided by CDs. As there are no studies which discuss whether the act of listening to any therapy will affect outcomes, we will also explore whether white noise can affect outcomes as well. Therefore, one control group (WN) will abide by the same regimen and will listen to a CD with white noise; the other control group (CP) will have no intervention at all and will follow our current peri-operative procedures.

Conditions

Interventions

TypeNameDescription
BEHAVIORALGuided imagery and music therapyParticipants will undergo a standardized regimen of peri-operative guided imagery and music therapy guided by CDs (compact disc). The peri-operative regimen will include: listening to the CD while in the pre-operative holding area, listening to the CD during the procedure; listening to the CD after the procedure beginning on the evening of post-operative day (POD)#0 and continuing twice a day until POD#3.
BEHAVIORALWhite NoiseControl group (WN) will listen to a CD with white noise. Participants' regimen will include: listening to the CD while in the pre-operative holding area, listening to the CD during the procedure; listening to the CD after the procedure beginning on the evening of post-operative day (POD)#0 and continuing twice a day until POD#3.
OTHERNo interventionControl group (CP) will have no intervention at all and will follow our current peri-operative procedures.

Timeline

Start date
2010-04-01
Primary completion
2013-04-01
Completion
2013-04-01
First posted
2011-01-26
Last updated
2014-08-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01284075. Inclusion in this directory is not an endorsement.