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Completed

NCT Number: NCT04169971

Investigation of the Effects of Music on Anxiety During Operations Under Spinal Anaesthesia at an Hospital in Cambodia

This study investigates he effects of intra-operative music on anxiety levels during procedures under spinal anaesthesia at a surgical centre in Cambodia. Participants will be randomly allocated to either the music (M) group or the 'control' (C) group. The M group will receive music played through headphones for the duration of the operation. The C group will receive no music or headphones. Anxiety will be measured in both groups, through a visual analogue scale (VAS), at the beginning of the operation and after 30 minutes of the procedure. Scores will be compared.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Children's Surgical Centre

Phnom Penh, Cambodia

About this study

Background: During operations conducted under spinal anaesthesia patients are aware of their environment, including sounds related to operative instruments and the voices of staff. This has the potential to cause anxiety and amplify existing anxiety which can negatively impact patient experience and outcomes. Research has shown peri-operative music can reduce anxiety but there is no robust evidence for the effect of intraoperative music on intraoperative anxiety.

Objectives: The primary objective is to determine the effects of intraoperative music on intraoperative anxiety levels for patients undergoing procedures conducted under spinal anaesthesia. The secondary objectives are to investigate whether participants feel that music improved/would improve their experience and whether they would choose it in future or recommend it for others.

Methods: This prospective randomised controlled trial will be conducted at the Children's Surgical Centre in Phnom Penh. Participants will be 18 years or over, due to undergo a procedure that requires spinal anaesthesia and not have a medical history that fulfils any of the exclusion criteria. The trial will aim to recruit between 16 and 28 patients consecutively once it commences, and participants will be randomised to either the music (M) group or the 'control' (C) group. The M group will receive music (pre-selected from 5 categories) played through headphones for the duration of the operation. The C group will receive no music or headphones. Anxiety will be measured in both groups, through a visual analogue scale (VAS), at the beginning of the operation and after 30 minutes of the procedure. In the recovery room the participants will be asked two questions relating to experience and future recommendations.

Results: The VAS scores and change in VAS scores will be displayed as mean ± Standard Error and the results from the two groups will be compared using a student's paired t-test or a Mann-Whitney U test depending on the distribution of the data. The results from the post-operation questions will be displayed as frequencies and the answers will be compared using a χ2 test. All tests will be 2-tailed and P<0.05 will be considered significant

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years of age and older
  • Undergoing a procedure at CSC that requires spinal anaesthesia and spinal anaesthesia is not contra-indicated
  • Gives informed consent to participate in the trial

Exclusion criteria

  • Has an existing psychological diagnosis
  • Has auditory impairment
  • Deemed not to have capacity to give consent
  • Sedatives are administered during the procedure
  • General anaesthesia is required during the procedure

Treatment and study plan

Music

Other

Played through headphones during the operation under spinal anaesthesia

Primary outcomes

  1. Change in intra-operative anxiety scores

    Time frame: Calculated between scores recorded at the start of the operation and 30 minutes into the procedure

    Score on 'Anxiety visual analogue scale.' Minimum score 0 representing calm and maximum score 10 representing extreme anxiety

Secondary outcomes

  1. Percentage of patient's in the music group who felt that music made the experience better, worse or had no effect.

    Time frame: Within 4 hours post operation

    Questionnaire asked verbally. What effect do you think music had on your experience during surgery? a) made it better b)made it worse c)no effect.

  2. Percentage of patient's in the music group who felt that they would recommend to others, wouldn't recommend to others or did not know.

    Time frame: Within 4 hours post operation

    Questionnaire asked verbally. Would you recommend listening to music during an operation to other people? a)yes b)no c) don't know

  3. Percentage of patient's in the control group who felt that music would have made their experience better, worse or the same.

    Time frame: Within 4 hours post operation

    What effect do you think music would have had on your experience during surgery? a) made it better b)made it worse c)no effect.

  4. Percentage of patient's in the music group who, if they had another operation, would like to listen to music, would not like to listen to music, or did not know.

    Time frame: Within 4 hours post operation

    Questionnaire asked verbally. Would you like to listen to music if you were to have another operation? a)yes b)no c) don't know

  5. Percentage of anaesthetic providers that experience problems due to music.

    Time frame: Within 4 hours post operation

    Questionnaire on data collection form. Do you think that the music caused any problems during the operation? a)yes b)no c)maybe

Sponsors and collaborators

Lead sponsor

Children's Surgical Center, Cambodia

Other

Registry information

Official study title

A Prospective Randomised Controlled Trial to Investigate the Effects of Intra-operative Music on Anxiety Levels During Procedures Under Spinal Anaesthesia at a Surgical Centre in Cambodia

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Nov 20, 2019
Registry last updated
Dec 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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