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The effects of Therapeutic Instrumental Music in improving the upper limb function and mood of stroke patients in a rehabilitation setting

The effects of rhythmic stimulation to improve upper limb function and mood of stroke patients in inpatient rehabilitation setting

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000926831
Acronym
TIMP
Enrollment
52
Registered
2012-08-30
Start date
2012-09-03
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Patients undergoing rehabilitation due to neurological diseases such as stroke, Parkinson’s disease, traumatic brain injury and spinal cord injury are often faced with significant physical and psychological stressors. Patients are often inattentive and not motivated during therapy sessions. Music therapy (MT), which is the clinical use of music interventions within a therapeutic relationship, has been shown to be of benefit to patients with neurological diseases in rehabilitation setting. The data on mood, attention and motivation level of patients undergoing rehabilitation in the neurology rehabilitation ward is, however, limited especially where music therapist is involved. Hence this pilot study aims to investigate the effectiveness of rhythmic stimulation on upper limb function and mood of stroke patients with undergoing rehabilitation in the inpatient neurology rehabilitation ward. The study design is a randomized controlled trial of 26 patients receiving standard rehabilitation together with MT intervention who will be compared with 26 patients receiving only standard rehabilitation as usual. The null hypotheses being tested are that there will be no significant differences in upper limb function, mood and participation level in ARAT, HADS, visual analog mood scale (Faces Scale, Andrews & Withey, 1976), and PRPS between the two groups of patients. The inclusion criteria for participation in the study include persons diagnosed either with ischaemic or haemorrhagic acute stroke undergoing daily occupation therapy for 10 sessions (exclude weekends and public holidays). Each standard occupational therapy session will last for up to 60 minutes, out of which up to 30 minutes will be focused on upper limb rehabilitation. The music therapy intervention will have up to 30 minutes therapy session and is provided daily by a board certified music therapist for a duration of 10 sessions (exclude weekends and public holidays). The components of the intervention include music rhythmic stimulation with movement exercises directed by occupational therapist.

Interventions

The study design is a randomized controlled trial of 26 patients receiving standard rehabilitation together with Music Therapy intervention who will be compared with 26 patients receiving only standard rehabilitation as usual. Each standard occupational therapy session will last for up to 60 minutes, out of which up to 30 minutes will be focused on upper limb rehabilitation. The music therapy intervention will have up to 30 minutes therapy session and is provided daily by a board certified mus

The study design is a randomized controlled trial of 26 patients receiving standard rehabilitation together with Music Therapy intervention who will be compared with 26 patients receiving only standard rehabilitation as usual. Each standard occupational therapy session will last for up to 60 minutes, out of which up to 30 minutes will be focused on upper limb rehabilitation. The music therapy intervention will have up to 30 minutes therapy session and is provided daily by a board certified music therapist for a duration of 10 sessions (exclude weekends and public holidays). The components of the intervention include music rhythmic stimulation with movement exercises directed by occupational therapis simultaneously. The exercise is sequential flexion-extension of elbow movements of one arm. All subjects in the study will received individualised therapy. All subjects in either condition will receive up to 60-minute intervention daily for a duration of 10 sessions (exclude weekends and public holidays). The follow-up will be 3 weeks.

Sponsors

Patsy Tan Lee Peng
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
21 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

Inclusion criteria: Patients diagnosed with stroke, who is at least 21 years of age or above and admitted to SGH Department of Rehabilitation Medicine between the period of November 2012 - October 2013. - Acquired brain injury, that is, stroke - First stroke patient referred for occupational therapy - MMSE greater or equal to 18 (Levels of impairment have also been classified as none (24-30); mild (18-23) and severe (0-17) (Tombaugh & McIntyre 1992) - Upper limb impairment Manual Muscle Testing (MMT) = 1, 2 or 3 - Medically stable to participate in an active rehabilitation program

Exclusion criteria

Exclusion criteria: * Individuals will be excluded if they have any other acute co-morbidities influencing their mobility, that is: - Patients with pre-existing upper limb impairments eg. Amputation, deformity, contracture - Patients with Parkinson's Disease - Patients with severe spasticity (MAS greater than or equal to 2) - Patients with severe hearing impairment * Patients recruited in other study

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026