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NCT06239948 Clinical Trial

The Brain Symphony For Post-Stroke Rehabilitation

Stroke Clinical Trial

Official title:
The Brain Symphony For Post-Stroke Rehabilitation - A Pilot Randomized Controlled Study With P.Ramlee Songs

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06239948
Other study ID # Brain Symphony
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2018
Est. completion date December 31, 2020

Study information
Verified date January 2024
Source University of Malaya
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Music listening intervention has made great strides in improving the condition of stroke survivors. Thus, this research explores the effects of music listening intervention on post-stroke survivors during rehabilitation by using P. Ramlee songs.

Description:

Objective: Music listening intervention has made great strides in improving the condition of stroke survivors. Thus, this research explores the effects of music listening intervention on post-stroke survivors during rehabilitation by using P. Ramlee songs. Materials & Methods: In the first phase, surveys were conducted to determine the selection of songs to be used in the second phase. The second phase is applying music listening intervention on a small sample of 20 subjects, aged 55 years old and above. The participants were categorized into two groups: stroke survivors and healthy individuals and randomized into control group (without music) and experimental group (with music). The second phase consists of three stages. Stage one is to pre-screen and select potential subjects before the experiment. The second stage aims to determine the effect of P. Ramlee music on stroke survivors during their rehabilitation through augmenting their brain neuroplasticity with measurement of the MEP using TMS. The final stage compares the effects of MEP between lesion and non-lesion areas.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 55 Years to 80 Years
Eligibility Inclusion Criteria: - Healthy - No history of seizures or epilepsy - Able to hear well - Able to attend experiment sessions without scheduling conflicts - No contraindications to undergoing TMS Exclusion Criteria: • None

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• With Music
each subject was placed in a TMS laboratory with music for 20 minutes
• Without Music
each subject was placed in a TMS laboratory without music for 20 minutes

Locations
Country Name City State
Malaysia Universiti Malaya Medical Centre Kuala Lumpur

Sponsors (1)
Lead Sponsor Collaborator
University of Malaya

Country where clinical trial is conducted

Malaysia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Transcranial Magnetic Stimulation (TMS) Wilcoxon signed-ranks test for the comparison of pre- and post- experiment 24 months
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