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Clinical Trials/NCT02776293
NCT02776293
Completed
Not Applicable

Prenatal Listening to Songs Composed for Pregnancy and Symptoms of Anxiety and Depression: a Pilot Study

Goldsmiths, University of London0 sites223 target enrollmentJanuary 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prenatal Anxiety
Sponsor
Goldsmiths, University of London
Enrollment
223
Primary Endpoint
State-Trait Anxiety Inventory
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Prenatal anxiety and depression are distressing for the expectant mother and can have adverse effects on her fetus and child. This study aimed to determine whether listening to specially composed songs would be an effective intervention for reducing symptoms of prenatal anxiety and depression over a period of 12 weeks.

Detailed Description

Prenatal anxiety and depression has negative implications for both the mother and the developing child, including developmental disorders, low birth weight, and altered immune function. It is therefore very important both to detect and to help ameliorate symptoms of anxiety and depression in pregnant women. Many women do not want pharmacological interventions at this time, and with less severe symptoms it may not be appropriate. Thus there is a need to find non-pharmacological methods of intervention. Psychological therapies such as cognitive behavioural therapy or interpersonal therapy can be effective. But these are often not available for the large numbers of women who could benefit. Though there has been evidence that music has the ability reduce anxiety, no study has quantitatively measured prenatal anxiety and depression over a long period of time. Proof of efficacy could justify investment into music as an inexpensive, and non-stigmatizing method to reduce prenatal anxiety and depression and therefore benefit both the mother and child.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
July 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lauren Stewart

Dr. Lauren Stewart

Goldsmiths, University of London

Eligibility Criteria

Inclusion Criteria

  • English speaking women
  • At least 18 years of age.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

State-Trait Anxiety Inventory

Time Frame: 12 weeks

Questionnaire measuring an individual's general level of anxiety (trait) and an individual's anxiety level at the time of taking the questionnaire (state).

Edinburgh Postnatal Depression Scale

Time Frame: 12 weeks

Questionnaire measuring symptoms of maternal depression

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