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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03028844
Other study ID # ED/01/16UCC
Secondary ID
Status Completed
Phase N/A
First received January 9, 2017
Last updated January 18, 2017
Start date April 2016
Est. completion date November 2016

Study information

Verified date January 2017
Source University College Cork
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Randomised Crossover Trial in Preterm Infants less than 32 weeks to assess Music therapy and sucrose versus sucrose on stress


Description:

The purpose of this study is to assess whether the use of music therapy as a non-pharmacological intervention around the time of venepuncture significantly decreases the stress response of a stable preterm neonate, as measured by salivary cortisol levels .

The secondary aim of this study is to analyse the effect of music therapy on the EEG, and vital signs of the stable preterm neonate.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date November 2016
Est. primary completion date November 2016
Accepts healthy volunteers No
Gender All
Age group 23 Weeks to 32 Weeks
Eligibility Inclusion Criteria:

- Infants born at less than 32 weeks gestational age (from 23+0 weeks' up to and including 31+6 weeks' gestational age)

- Infants must now be >32 weeks corrected gestational age

- Infants who are medically stable and due to have routine venepuncture as part of their management plan

Exclusion Criteria:

- Inability to obtain informed consent from parent

- Infants with known hearing impairment

- Infants receiving sedative medications

- Any evidence of dysfunction of the hypothalamic-pituitary-adrenal axis

- Infants with congenital abnormalities

- Infants with known EEG abnormalities

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Music therapy
The musical intervention will be played for ten minutes prior to venepuncture

Locations

Country Name City State
Ireland Cork University Maternity Hospital Cork

Sponsors (1)

Lead Sponsor Collaborator
University College Cork

Country where clinical trial is conducted

Ireland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Salivary cortisol levels Change in salivary cortisol levels between Baseline, 20 minutes and 4 hours BASELINE, 20 mins and 4 hours
Secondary Premature Infant Pain Profile (PIPP) score Alteration in pain as measured by Premature Infant Pain Profile (PIPP) score immediate
Secondary Changes in physiological parameters - Heart rate Increase in heart rate 10 mins before venepuncture and 10 mins after
Secondary Changes in physiological parameters - respiration rate Increase in respiration rate 10 mins before venepuncture and 10 mins after
Secondary Changes in physiological parameters - oxygen saturation Decrease in oxygen saturation 10 mins before venepuncture and 10 mins after
Secondary Changes in physiological parameters - EEG Altered EEG amplitude and Frequency. 10 mins before venepuncture and 10 mins after
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