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Individualized Music Versus Propofol for Perioperative Anxiety During Regional Anaesthesia

2026년 9월 10일 업데이트: University of Malaya

Comparing Professionally-prescribed Music by Music Therapist Versus Standard Practice Using Intravenous Sedative-hypnotic Agents on the Anxiolytic and Sedative Effect During Regional Anaesthesia: A Randomized Controlled Trial

Perioperative anxiety is common among patients undergoing surgery under regional anaesthesia. Intravenous sedative-hypnotic agents such as propofol are commonly administered to reduce anxiety and improve patient comfort; however, pharmacological sedation may reduce patient alertness and cause cardiorespiratory adverse effects. Music may provide a non-pharmacological alternative for reducing perioperative anxiety.

This prospective controlled study compared professionally prescribed individualized music with intravenous propofol sedation in adult patients undergoing surgery under regional anaesthesia. Participants in the music group received an individualized playlist curated by a professional music therapist following assessment of their music preferences and listening history. Participants in the sedative-hypnotic group received intravenous propofol sedation titrated according to clinical assessment.

Perioperative anxiety was assessed before and after surgery using the State-Trait Anxiety Inventory-State (STAI-S) and a visual analogue scale (VAS). Intraoperative sedation and alertness were assessed using the Bispectral Index (BIS) and Modified Observer's Assessment of Alertness/Sedation (mOAA/S), together with haemodynamic monitoring and patient satisfaction.

연구 개요

상세 설명

This was a prospective, single-centre, parallel-group controlled study conducted at University Malaya Medical Centre, Kuala Lumpur, Malaysia. Adult patients scheduled for surgery under regional anaesthesia were allocated to either a music-therapy group or a sedative-hypnotic group according to their scheduled operating day.

Participants assigned to the music intervention underwent a preoperative assessment by a professional music therapist. The assessment included the participant's music-listening history and preferences, following which an individualized playlist was curated for intraoperative listening through headphones.

Participants assigned to the sedative-hypnotic group received intravenous propofol using target-controlled infusion, titrated according to clinical assessment and sedation monitoring.

Anxiety was evaluated preoperatively and postoperatively using STAI-S and an anxiety VAS. Intraoperative BIS, mOAA/S, haemodynamic variables and relevant rescue interventions were recorded. Postoperative patient satisfaction was also assessed.

The study received approval from the Medical Research Ethics Committee, University Malaya Medical Centre (MREC ID 2023418-12366), before participant recruitment, and written informed consent was obtained from all participants. The study was completed before registration on ClinicalTrials.gov.

연구 유형

중재적

등록 (실제)

60

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Federal Territory of Kuala L
      • Kuala Lumpur, Federal Territory of Kuala L, 말레이시아, 59100
        • University Malaya Medical Centre

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  • Age 18 to 70 years.
  • American Society of Anesthesiologists (ASA) physical status I or II.
  • No sedative or anxiolytic medication received before surgery that could affect measurement of vital signs or Bispectral Index (BIS).
  • Able to understand and communicate in Malay or English, understand the purpose and objectives of the study, and provide written informed consent.
  • Surgery planned under regional anaesthesia (spinal, epidural, or peripheral nerve block).
  • Surgery performed in the supine position.

Exclusion Criteria:

  • Received general anaesthesia.
  • Refused to participate.
  • Hearing impairment.
  • Diagnosed neurocognitive or psychiatric disorder.
  • Aggressive or uncooperative behaviour.
  • Surgery duration exceeding 3 hours.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 지지 요법
  • 할당: 무작위화되지 않음
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Professionally Prescribed Individualized Music
Participants received professionally prescribed individualized music during surgery under regional anaesthesia. Before surgery, a professional music therapist assessed each participant's music-listening history and preferences and curated an individualized playlist. Music was delivered intraoperatively through headphones. Rescue intravenous sedation could be administered when clinically required.
Participants underwent a preoperative music assessment by a professional music therapist that included music-listening history and individual preferences. Based on this assessment, the music therapist curated an individualized playlist for each participant. The prescribed music was delivered intraoperatively through headphones during surgery under regional anaesthesia. Participants remained awake without routine intravenous sedation, although rescue sedation could be administered when clinically required.
활성 비교기: Intravenous Propofol Sedation
Participants received intravenous propofol sedation during surgery under regional anaesthesia using target-controlled infusion. Propofol was titrated according to clinical assessment and sedation monitoring.
Participants received intravenous propofol sedation by target-controlled infusion during surgery under regional anaesthesia. Sedation was titrated according to clinical assessment using Bispectral Index (BIS) and Modified Observer's Assessment of Alertness/Sedation (mOAA/S) monitoring.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change in State Anxiety Measured by the State-Trait Anxiety Inventory-State (STAI-S)
기간: Perioperative period: During preoperative assessment at the operating theatre reception bay; And during postoperative assessment in the post-anaesthesia recovery room, on the day of surgery
State anxiety was assessed using the 20-item State-Trait Anxiety Inventory-State (STAI-S) before and after surgery. The total score ranges from 20 to 80, with higher scores indicating greater state anxiety. The outcome was the change in STAI-S score from the preoperative to the postoperative assessment.
Perioperative period: During preoperative assessment at the operating theatre reception bay; And during postoperative assessment in the post-anaesthesia recovery room, on the day of surgery

2차 결과 측정

결과 측정
측정값 설명
기간
Change in Anxiety Visual Analogue Scale (VAS) Score
기간: Perioperative period: During preoperative assessment at the operating theatre reception bay; And during postoperative assessment in the post-anaesthesia recovery room, on the day of surgery
Anxiety was assessed using a Visual Analogue Scale (VAS) ranging from 1 (least anxious) to 10 (most anxious), with higher scores indicating greater anxiety. The outcome was the change in VAS score from the preoperative to the postoperative assessment.
Perioperative period: During preoperative assessment at the operating theatre reception bay; And during postoperative assessment in the post-anaesthesia recovery room, on the day of surgery
Intraoperative Bispectral Index (BIS)
기간: Every 10 minutes from the start of surgery until completion of surgery.
Depth of sedation was assessed using the Bispectral Index (BIS). BIS values were recorded at 10-minute intervals during surgery to assess the level of sedation during the assigned intervention.
Every 10 minutes from the start of surgery until completion of surgery.
Intraoperative Level of Sedation Measured by Modified Observer's Assessment of Alertness/Sedation (mOAA/S)
기간: Every 10 minutes from the start of surgery until completion of surgery.
Alertness and sedation were assessed using the modified Observer's Assessment of Alertness/Sedation (mOAA/S) scale, ranging from 0 to 5. A score of 5 indicates that the participant is alert and responds readily to their name spoken in a normal tone, whereas a score of 0 indicates no response to a painful trapezius squeeze. Higher scores therefore indicate greater alertness and lower levels of sedation. mOAA/S was assessed at 10-minute intervals during surgery.
Every 10 minutes from the start of surgery until completion of surgery.
Intraoperative Systolic Blood Pressure
기간: Every 10 minutes from the start of surgery until completion of surgery.
Systolic blood pressure was recorded at 10-minute intervals during surgery to assess haemodynamic changes during the assigned intervention.
Every 10 minutes from the start of surgery until completion of surgery.
Intraoperative Diastolic Blood Pressure
기간: Every 10 minutes from the start of surgery until completion of surgery
Diastolic blood pressure was recorded at 10-minute intervals during surgery to assess haemodynamic changes during the assigned intervention.
Every 10 minutes from the start of surgery until completion of surgery
Intraoperative Heart Rate
기간: Every 10 minutes from the start of surgery until completion of surgery
Heart rate was recorded at 10-minute intervals during surgery to assess haemodynamic changes during the assigned intervention.
Every 10 minutes from the start of surgery until completion of surgery
Postoperative Patient Satisfaction
기간: Postoperative period: During assessment in the post-anaesthesia recovery room, on the same day of surgery
Overall satisfaction with the intervention provided during surgery was assessed using a verbal numerical rating scale ranging from 1 (least satisfied) to 10 (most satisfied), with higher scores indicating greater satisfaction.
Postoperative period: During assessment in the post-anaesthesia recovery room, on the same day of surgery

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: MOHD FITRY BIN ZAINAL ABIDIN, University of Malaya

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2023년 8월 7일

기본 완료 (실제)

2024년 3월 13일

연구 완료 (실제)

2024년 3월 13일

연구 등록 날짜

최초 제출

2026년 9월 4일

QC 기준을 충족하는 최초 제출

2026년 9월 10일

처음 게시됨 (실제)

2026년 9월 15일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 15일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 10일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

There is currently no plan to make individual participant data publicly available.

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아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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