Effects of Music on Acute Postoperative Pain Intensity and Mobility After Fragility Hip Fracture

February 17, 2024 updated by: Lau Kwan Yiu Jeffrey, Hospital Authority, Hong Kong

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

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Hong Kong, Hong Kong
        • Recruiting
        • Ward G9, Queen Elizabeth Hospital
        • Contact:
        • Principal Investigator:
          • Kwan Yiu Jeffrey Lau

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Emergency admitted to QEH/G9 due to fragility hip fracture (#NOF or # TOF) within the study period
  2. Plan for surgical intervention
  3. Able to provide written informed consent
  4. Able to communicate in Cantonese/ Putonghua/ English

Exclusion Criteria:

  1. History of dementia
  2. Acute delirium upon admission
  3. Disorientated to time, person or place
  4. Concurrent fracture at other sites
  5. Utilization of other analgesics on top of pain protocol
  6. Appreciable deficits in hearing or vision
  7. Hemodynamically unstable
  8. Plan for neurolysis/ nerve block as definite treatment or opt for conservative treatment

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 26, 2024

Primary Completion (Estimated)

June 1, 2024

Study Completion (Estimated)

June 1, 2024

Study Registration Dates

First Submitted

February 8, 2024

First Submitted That Met QC Criteria

February 17, 2024

First Posted (Actual)

February 26, 2024

Study Record Updates

Last Update Posted (Actual)

February 26, 2024

Last Update Submitted That Met QC Criteria

February 17, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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