Effect of Music Listening on Stress in Acute Stroke

NCT ID: NCT05859841

Last Updated: 2023-05-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-08-21

Study Completion Date

2023-06-30

Brief Summary

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Investigation on changes in the neurochemical stress parameters in acute stroke. 30 patients are recruited in the stroke unit, blood samples are collected at fixed intervals during the first two days. Patients are randomized to music listening and control.Neuropsychological testing is performed in the acute phase and 6 months post-stroke.

Detailed Description

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Outcome measures: NIHSS, stress hormone levels, questionnaires on mood and quality of life.

Conditions

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Acute Stroke

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

15 pt listen to music, 15 receives standard treatment, care and rehabilitation
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Music listening

Music listening under instruction by music therapist, min 3 hours daily

Group Type EXPERIMENTAL

Music listening

Intervention Type OTHER

Music listening under instruction by music therapist, min 3 hours daily

Control

Standard treatment, care and rehabilitation

Group Type PLACEBO_COMPARATOR

Control

Intervention Type OTHER

Standard treatment, care and rehabilitation

Interventions

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Music listening

Music listening under instruction by music therapist, min 3 hours daily

Intervention Type OTHER

Control

Standard treatment, care and rehabilitation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Hemispheric infarction
* Neurologically stable

Exclusion Criteria

* Previous neurological disease affecting the outcome
* Previous psychiatric disease affecting the outcome
* Substance abuse
Minimum Eligible Age

60 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Helsinki

OTHER

Sponsor Role collaborator

Turku University Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Seppo Soinila

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Susanna Tuomaala

Role: STUDY_CHAIR

Chief of Research

Locations

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Turku University Hospital

Turku, , Finland

Site Status

Countries

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Finland

Other Identifiers

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34/1801/2017

Identifier Type: -

Identifier Source: org_study_id

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