- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06277102
Effects of Music on Acute Postoperative Pain Intensity and Mobility After Fragility Hip Fracture
Effects of Music on Acute Postoperative Pain Intensity and Mobility After Fragility Hip Fracture: A Randomized Controlled Trial
Music has been proven to be beneficial in postoperative care by reducing pain. The effects of music listening to reduce pain postoperatively are well studied among cases undergoing elective orthopaedic surgery. No study has been conducted focusing on pain control among cases with fragility hip fractures in an acute ward setting with non-schedule non-elective orthopaedic operation.
In Queen Elizabeth Hospital a standardized analgesic protocol is used for all fragility hip fracture cases unless contraindicated, a suboptimal post-operative pain control is not uncommonly seen. Stepping up analgesics is usually a concern in the elderly with a higher rate of side effects, a safe and simple non-pharmacological intervention for pain control is therefore needed.
The aim of this study is to study the effectiveness of incorporating music on pain intensity and mobility with the standard postoperative rehabilitation care of fragility hip fracture in Queen Elizabeth Hospital.
Study Overview
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Kwan Yiu Jeffrey Lau
- Phone Number: 62017014
- Email: lky194a@ha.org.hk
Study Locations
-
-
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Hong Kong, Hong Kong
- Recruiting
- Ward G9, Queen Elizabeth Hospital
-
Contact:
- Kwan Yiu Jeffrey Lau
- Phone Number: 62017014
- Email: lky194a@ha.org.hk
-
Principal Investigator:
- Kwan Yiu Jeffrey Lau
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Emergency admitted to QEH/G9 due to fragility hip fracture (#NOF or # TOF) within the study period
- Plan for surgical intervention
- Able to provide written informed consent
- Able to communicate in Cantonese/ Putonghua/ English
Exclusion Criteria:
- History of dementia
- Acute delirium upon admission
- Disorientated to time, person or place
- Concurrent fracture at other sites
- Utilization of other analgesics on top of pain protocol
- Appreciable deficits in hearing or vision
- Hemodynamically unstable
- Plan for neurolysis/ nerve block as definite treatment or opt for conservative treatment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control
Standard of care
|
|
Experimental: Music
Music listening at postoperative day 1 and 2, 1 session per day, 20 minutes per session.
|
Music listening at postoperative day 1 and 2, 1 session per day, 20 minutes per session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Pain intensity measured by 11-point pain intensity numerical rating scale after music listening in postoperative Day 1 - 2 among subjects with fragility hip fracture
Time Frame: postoperative day 1 and 2
|
postoperative day 1 and 2
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Modified functional ambulatory classification (MFAC) in postoperative Day 3 among subjects with fragility hip fracture
Time Frame: postoperative day 3
|
postoperative day 3
|
New mobility score (NMS) in postoperative Day 3 among subjects with fragility hip fracture
Time Frame: postoperative day 3
|
postoperative day 3
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Music pain FHF
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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