Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
ID04708808

The Efficacy of Music as an Adjunct Analgesic in Reducing Pain and Anxiety During Ultrasound-guided Manual Vacuum Aspiration (USG-MVA): A Randomized Controlled Trial

Led by Chinese University of Hong Kong · Updated on 2026-05-07

176

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of music therapy as an additional pain control method during ultrasound-guided manual vacuum aspiration (USG-MVA), a surgical treatment for early pregnancy loss. This procedure is safer and more cost-effective than traditional surgery but often causes significant pain and anxiety. The study aims to see if music can reduce pain and anxiety levels experienced by women undergoing USG-MVA, addressing both physical discomfort and psychological distress. Participants are randomly assigned to two groups: one receives routine USG-MVA care plus music therapy via Bluetooth headphones playing their chosen music during the procedure, while the other group receives routine care without music. Routine care includes oral medications like Misoprostol for cervical priming, naproxen or alternatives for pain, and local anesthesia during the procedure. Music therapy starts when the patient is positioned and ends when the procedure is complete. Women in the study will rate their pain using a visual analog scale before, during, immediately after, and two hours after the procedure. Anxiety and stress levels are measured with questionnaires and saliva tests for stress biomarkers. Researchers will assess pain and anxiety differences between groups, patient satisfaction, and physiological stress responses. The study includes follow-up visits and aims to analyze data using statistical software to determine the impact of music therapy on pain and anxiety during USG-MVA.

CONDITIONS

Brief Title

The Effect of Music Therapy Under Ultrasound Guided Manual Vacuum Aspiration

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women 18 years old or above
  • Hospitalized for termination of first trimester pregnancy under local anaesthesia
  • Feasible for USG-MVA procedure
Not Eligible

You will not qualify if you...

  • Being a minor or adult protected by law
  • Not feasible for MVA procedure
  • Partial or total hearing impairment
  • Taking anxiolytics or analgesics before arriving at the hospital
  • Refusal to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) for eligibility assessment and consent

Treatment

Duration - Single day procedure

Participants undergo ultrasound-guided manual vacuum aspiration (USG-MVA) with or without music therapy during the procedure to evaluate pain and anxiety levels.

1 visit (in-person) on the day of the procedure

Follow-up

Duration - Up to 3 weeks after the procedure

Participants are observed for post-procedure outcomes including pain, anxiety, physiological stress, and satisfaction. A pregnancy test is done to evaluate completeness of evacuation.

1 follow-up visit approximately 3 weeks after the procedure

Trial Site Locations

Total: 1 location

1

Chinese University of Hong Kong

Hong Kong, Shatin, Hong Kong

Actively Recruiting

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Research Team

H

Hiu Tan Margaret Lee

P

Pui Wah Jacqueline Chung, MBBS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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