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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05374096
Other study ID # 22-286
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 13, 2022
Est. completion date July 17, 2023

Study information

Verified date July 2023
Source The Cleveland Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess whether listening to music during surgery has an effect on pain or anxiety after surgery.


Description:

After being informed about the study and potential risks and meeting eligibility criteria, all patients giving written informed consent will be scheduled for their hernia repair surgery. On the day of surgery, patients will be randomized in a double-blind manner (participant and investigator) in a 1:1 ratio to listen to patient-chosen music during their surgery via headphones or just listen to silence via headphones. Pain and anxiety will then be assessed after surgery.


Recruitment information / eligibility

Status Completed
Enrollment 321
Est. completion date July 17, 2023
Est. primary completion date July 15, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Adults having open retromuscular ventral hernia repair with mesh, with or without myofascial release for a hernia width = 20 cm 2. Adults having open flank hernia repair that requires a myofascial release with mesh 3. Adults having parastomal hernia repair with mesh Exclusion Criteria: 1. Primary language other than English, or lack of English language fluency 2. Hearing impairment, with or without use of hearing aids 3. Neurologic condition that, in the opinion of the investigators, may preclude accurate assessment of postoperative pain and anxiety 4. Patients who will remain intubated after surgery

Study Design


Intervention

Other:
Patient-Chosen Music
Music played into headphones.
Placebo
Silence into headphones.

Locations

Country Name City State
United States Cleveland Clinic Main Campus Cleveland Ohio

Sponsors (1)

Lead Sponsor Collaborator
The Cleveland Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Post operative Pain - 3 days Pain scores will be assessed using the Numeric Pain Rating Scale (NRS-11); The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable") Collected at 3 time points after surgery end time - 24 hours (+- 3 hours), 48 hours (+-3 hours) and 72 hours (+-3 hours)
Other Post operative Pain - cumulative Pain scores will be assessed using the Numeric Pain Rating Scale (NRS-11); The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable") Will be collected repeatedly by nursing staff per nursing protocol for the first 24 hours after surgery end time.
Other Post operative Anxiety - 3 days Anxiety scores will be assessed using State Trait Anxiety Index-6 (STAI-6) Anxiety tool (a 6 question patient-reported anxiety assessment). The higher the total, the greater the anxiety is. Collected at 3 time points after surgery end time - 24 hours (+- 3 hours), 48 hours (+-3 hours) and 72 hours (+-3 hours)
Other Post operative opioid consumption Cumulative opioid consumption converted into morphine milligram equivalents. During the first 72 hours after surgery end time.
Other Intraoperative sedative use Total number of intravenous and inhaled anesthetics, benzodiazepines, and opioid medications. From induction of anesthesia to arrival in the post anesthesia care unit on the day of procedure
Primary Post operative Pain Pain scores will be assessed using the Numeric Pain Rating Scale (NRS-11); The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable") At 24 hours (+- 3 hours) after surgery end time.
Secondary Post operative Anxiety Anxiety scores will be assessed using State Trait Anxiety Index-6 (STAI-6) Anxiety tool (a 6 question patient-reported anxiety assessment). The higher the total, the greater the anxiety is. At 24 hours (+- 3 hours) after surgery end time.
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