- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04243967
Music Therapy Pathway in Patients Undergoing Total Laparoscopic Hysterectomy
Music Therapy Pathway to Reduce Preoperative Anxiety in Patients Undergoing Total Laparoscopic Hysterectomy for Benign Disease: a Randomized Controlled Trial
Music therapy is a non-invasive, safe, and inexpensive intervention that can be easily and successfully delivered. it has been shown that music therapy might reduce the postoperative pain in patients undergoing cesarean section and in those with cancer, showing a lower state of anxiety and greater pain reduction in participants who received music interventions.
The aim of the present study is to investigate the role of music and music therapy on anxiety and perception of pain in patients undergoing elective hysterectomy for benign disease.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hysterectomy is the second most common surgical procedure in the United States. Uterine fibroids (with or without the association of heavy menstrual bleeding) represent the primary indication for surgery. Prospective controlled trials have shown that the laparoscopic approach guarantees benefits in terms of perioperative surgical outcomes and better patients' quality of life if compared with open surgery. Music is a non-invasive, safe, and inexpensive intervention that can be delivered easily and successfully. Results of a recent meta-analysis of 73 RCTs demonstrated that music could be offered as a way to help patients reducing pain and anxiety during the postoperative period. Recently a prospective randomized trial demonstrated a reduction of anxiety also in patients undergoing gynecological minor procedures (office hysteroscopy). Thanks to the use of a validated scale for assessing the preoperative and postoperative level of anxiety (STAI: State-Trait Anxiety Inventory), an Italian group demonstrated an average reduction of approximately 5 points of STAI score in patients enrolled for listening to music before surgery compared to the control group (without music). Similarly, a RCT demonstrated that preoperative music intervention might also reduce the postoperative pain in patients undergoing cesarean section (reduction of 1.35 VAS points at 6 hours). A recent meta-analysis evaluated music interventions for improving psychological and physical outcomes in adult and pediatric patients with cancer, showing a lower state of anxiety and greater pain reduction in participants who received music interventions.
No study has been performed that aimed to investigate the role of music on anxiety and perception of pain in patients undergoing elective hysterectomy for benign disease, up to now.
A comparison with a superiority trial is required to evaluate the effects of music played preoperatively in women undergoing total laparoscopic hysterectomy for benign disease. Our findings will offer evidence in favor of the use of music therapy as a method to reduce perioperative anxiety and postoperative pain.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Varese, Italy
- Women's and Children "Del Ponte" Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adult women (45-55 years)
- Scheduled for total laparoscopic hysterectomy (+/- salpingectomy or salpingo-oophorectomy)
- Indication for surgery: presumed benign gynecologic disease
Exclusion Criteria:
- Any other associated non-gynecologic procedure to hysterectomy
- History of previous malignancy
- Individuals with hearing impairment (total or partial hearing difficulties)
- Patients with neuropathic pain/chronic pain needing regular anti-inflammatory drugs
- Non-Italian speaking patients
- Inability to provide informed consent
- Currently enrolled in any other research study involving drugs or devices
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MUSIC THERAPY
|
On the surgery day, the patient is accompanied by music-therapist all the way from her room to the operating theatre in order to monitor and adapt music-therapy intervention. The patient, prior to the anesthetic, take faces 3 phases of music therapy intervention (1 hour):
Other Names:
|
|
Experimental: CONTROL
|
Standard perioperative management including perioperative care (without the use of music / music therapy)
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anxiety
Time Frame: The same day of the surgery, before anesthesia
|
Preoperative - HADS scale assessment
|
The same day of the surgery, before anesthesia
|
|
Anxiety
Time Frame: Within 24 hours after surgery
|
Early postoperative - HADS scale assessment
|
Within 24 hours after surgery
|
|
Anxiety
Time Frame: At 1-month follow-up clinical evaluation
|
Late postoperative - HADS scale assessment
|
At 1-month follow-up clinical evaluation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain (VAS)
Time Frame: 1 hour after the end of the surgery
|
VAS 1 - Visual Analogic Scale assessment
|
1 hour after the end of the surgery
|
|
Pain (VAS)
Time Frame: 3 hours after the end of the surgery
|
VAS 3 - Visual Analogic Scale assessment
|
3 hours after the end of the surgery
|
|
Pain (VAS)
Time Frame: 8 hours after the end of the surgery
|
VAS 8 - Visual Analogic Scale assessment
|
8 hours after the end of the surgery
|
Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UInsubria_Gyn_19TLH
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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