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Measuring the Effects of Music-Listening On Distress After Intensive Care
Measuring the Effects of Music-Listening On Distress After Intensive Care

NCT07762196

Not Yet RecruitingNA

Sponsor: University of Edinburgh

Conditions: Post-ICU Patients, PICS

Interventions: Music intervention

Countries: United Kingdom

The primary goal of this single-case experimental design study is to investigate the effectiveness of personalised music listening on daily levels of distress after discharge from a critical care ward. The study will also aim to understand the effect of personalised music listening on symptoms of post-traumatic stress, anxiety, depression and health-related quality of life post-discharge. The main questions the study aims to answer are included below. After discharge from critical care, does personalised music-listening: * Reduce psychological distress? * Reduce symptoms of anxiety and depression? * Improve health-related quality of life (HRQoL)? The study will have 3 phases, allowing for participant data gathered during the baseline phase (treatment as usual) to be compared to data gathered during intervention (music-listening) and follow-up phases. Participants will: * rate their distress on a visual analogue scale each day. * listen to a minimum of 30 minutes of self-selected music each day during the intervention phase. * complete measures of mood, anxiety, post-traumatic stress and health-related quality of life at baseline, intervention and follow-up phases.

Eligibility overview

Sex: ALL

Age: 18 Years to

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* 18 years or older.
* Experienced an admission to an ICU/HDU of any length and not yet participated in InS:PIRE.
* Access to an internet-enabled device and internet connection whilst at home.
* Experiencing some distress relating to their ICU/HDU admission - a cut-off score of 4 on the VAS 'Distress Thermometer' has been used previously (Hofhuis et al., 2025).

Exclusion Criteria:

* Are unable to give informed consent e.g. have a significant cognitive impairment due to illness, injury or neurological condition, or are currently experiencing delirium or acute psychotic illness.
* Have significant communication difficulties or limited English and cannot access validated outcome measures or translation services in the given language.
* Are experiencing a mental health crisis or have recently attempted suicide, where ongoing significant risk of harm to themselves or others remains.
* Have an uncorrected hearing impairment that would prevent them from hearing their music playlist.
* Are participating in another study aimed at reducing distress.
Locations (1)
  • Kirkcaldy, Fife, United Kingdom