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Creative Practice as Mutual Recovery

Creative Practice as Mutual Recovery: Connecting Communities for Mental Health and Wellbeing

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01906892
Enrollment
150
Registered
2013-07-24
Start date
2013-11-30
Completion date
2015-04-30
Last updated
2015-11-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Individuals Experiencing Mild or Moderate Mental Health Issues

Brief summary

This study explores the hypothesis that mental health service users, their carers and musicians can - through the creative act of music learning and performing - mutually enhance wellbeing through the development of more meaningful and resilient lives. The project seeks to explore three interconnected issues: (i) the extent to which music learning and performing provides a forum for 'mutual recovery' among adult mental health service users, their formal/informal carers, and musicians, (ii) the characteristic features of 'mutual recovery' through music, and (iii) the underlying mechanisms of such 'mutual recovery'. The study will consist of three different stages. Stages 1 and 2 will examine the effect of a variety of group activities - including participatory music, listening to live music, listening to recorded music and a non-music control - on psychological scales, saliva samples of stress hormones and cytokines, and subjective experience to see which provide the most relaxing, sociable and supportive environments for mutual recovery. Stage 3 will explore the impact of musical interventions over longer periods of time. A systematic review we have just carried out has revealed a major gap in research comparing different music interventions and testing the effects of different lengths of interventions. As a result, our study should help us answer the following questions: * Which aspect(s) of music can contribute to mutual recovery? * Do carers, patients and musicians all respond to the same activities, or do some musical activities suit certain groups more than others? * Do carers, patients and musicians all recover at the same rate? * What length of intervention is most effective? If certain interventions are found to produce stronger results than others, these results could help guide community groups and healthcare settings in their design of music activities and have implications for the spending of arts-in-health budgets.

Interventions

OTHERGroup drumming (participatory)

Active participation in group drumming workshops

OTHERGroup drumming (live)

Listening to live performances of group drumming

OTHERGroup drumming (recorded)

Listening to recorded performances of group drumming

OTHERComparative activity

Taking part in a literary-based activity

Sponsors

Royal College of Music
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Individuals of either gender and over the age of 18 who are experiencing mild or moderate mental health issues including but not limited to: stress, anxiety, depression etc. * Individuals of either gender and over the age of 18 who formally or informally care for mental health service users. * Musicians who are professional workshop leaders and music students training to be professional musicians.

Exclusion criteria

* Serious mental health problems which might 1. prevent an individual from giving informed consent 2. cause the individual to be a disruption to other participants * Individuals for whom the music activity might conflict with other routine care. * Individuals with gum disease which would invalidate saliva samples. * Total deafness or severely impaired hearing. * Musicians or music students who apply to participate in the project but who are not deemed to have sufficient experience or expertise.

Design outcomes

Primary

MeasureTime frame
Warwick-Edinburgh Mental Well-being ScaleChange from baseline (recorded in the week prior to participation in either 6 or 10 weeks of music interventions) to the end of participation in the music interventions

Secondary

MeasureTime frame
Secker's 'Measure of social inclusion for arts and mental health project participants'Change from baseline (recorded in the week prior to participation in either 6 or 10 weeks of music interventions) to (a) the end of participation in the music interventions, and (b) 3 months after the end of music interventions
Connor-Davidson Resilience Scale (CD-RISC)Change from baseline (recorded in the week prior to participation in either 6 or 10 weeks of music interventions) to (a) the end of participation in the music interventions, and (b) 3 months after the end of music interventions
Hospital Anxiety and Depression ScaleChange from baseline (recorded in the week prior to participation in either 6 or 10 weeks of music interventions) to (a) the end of participation in the music interventions, and (b) 3 months after the end of music interventions
Blood pressureChange from baseline (taken immediately before the music intervention) when measured immediately following the 60 or 90 minute music intervention session
Saliva levels of salivary immunoglobulin AChange from baseline (taken immediately before the music intervention) when measured immediately following the 60 or 90 minute music intervention session
Saliva levels of interleukins including IL6Change from baseline (taken immediately before the music intervention) when measured immediately following the 60 or 90 minute music intervention session
Heart rateChange from baseline (taken immediately before the music intervention) when measured immediately following the 60 or 90 minute music intervention session
Saliva levels of cortisolChange from baseline (taken immediately before the music intervention) when measured immediately following the 60 or 90 minute music intervention session

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026