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The Impact of Creative Interventions on Symptoms of Postnatal Depression

The Impact of Creative Interventions on Symptoms of Postnatal Depression

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02526407
Enrollment
153
Registered
2015-08-18
Start date
2015-10-19
Completion date
2016-09-30
Last updated
2017-04-13

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

Conditions

Depression, Postpartum

Keywords

postnatal depression, mental wellbeing, baby blues, mothers, music, alternative therapies

Brief summary

Post-natal depression (PND) is anticipated to affect 12.9% of new mothers with at least 75,000 cases per year in the UK alone. However, despite this, there is currently a worrying lack of support for new mothers, with data suggesting that 64% of healthcare trusts in the UK do not have a strategy for treating postnatal depression, and flaws in the current pharmacological and psychological treatment models. Consequently, research into promising psychosocial interventions such as music is critical to developing new paradigms for treating postnatal depression. This project is an ambitious programme of research that investigates the effects of music on postnatal depression through two phases: a questionnaire study and an intervention study. This record is for the intervention study. The questionnaire study has a separate record. We are accepting host hospital sites for both.

Detailed description

The study tests the effectiveness of singing interventions led by the Royal College of Music at Chelsea and Westminster Hospital as a psychosocial tool to reduce the occurrence and effects of postnatal depression. It triangulates psychological, physiological, and biological data in a randomised control design to provide a comprehensive insight into the intervention's effects in comparison to a more common psychosocial intervention for new mothers (play groups) and a control group of no psychosocial interventions. The study aims to recruit 50-80 women into each of the three interventions (150-240 total). The study will used a mixed-method methodology comprising validated psychological scales, in-depth qualitative interviews and observations and biomarker analysis. If results are promising, there are plans in place to scale the singing intervention to more hospitals and community settings. Phase B will be open to NHS sites within the region of Chelsea and Westminster Hospital London from which women could travel to the sessions to take part.

Interventions

BEHAVIORALSinging

Sessions will be led by a professional practitioner assisted by students from the Royal College of Music. Participants will learn songs with their babies and help to create new musical material together.

BEHAVIORALGroup play

Sessions will be led by a professional practitioner assisted by students from the Royal College of Music. Participants will take part in group play activities.

Sponsors

Chelsea and Westminster NHS Foundation Trust
CollaboratorOTHER
Imperial College London
CollaboratorOTHER
Royal College of Music
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women who have a child up to 9 months old * Symptoms suggestive of PND at a minimum score of 10 on the EPDS

Exclusion criteria

* Outside the limits of the number of weeks pregnant/post birth * Living outside England * Refusal to participants

Design outcomes

Primary

MeasureTime frameDescription
Postnatal depressionChange from baseline at 6 weeks and 10 weeksMeasured with the Edinburgh Postnatal Depression Scale

Secondary

MeasureTime frameDescription
Mental wellbeingChange from baseline at 6 weeks and 10 weeksMeasured with the short Warwick-Edinburgh Mental Wellbeing Scale
Self-esteemChange from baseline at 6 weeks and 10 weeksMeasured with the Rosenberg Self-esteem scale
Social functioningChange from baseline at 6 weeks and 10 weeksMeasured with the Social Provisions Scale
Inflammatory immune responseChange from baseline at 6 weeks and 10 weeksMeasured with saliva samples to test for cortisol and cytokine activity

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026