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Choir Singing in Aphasia Rehabilitation

U

University of Helsinki

Status

Completed

Conditions

Stroke
Aphasia

Treatments

Behavioral: Singing-based rehabilitation
Other: Standard care

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study evaluates the verbal, cognitive, emotional, and neural efficacy of a choir singing intervention in chronic aphasic patients and their caregivers. Using a cross-over RCT design, half of the participants receive a 4-month singing intervention during the first half of the study and half of the participants during the second half of the study.

Full description

BACKGROUND: Singing is a highly stimulating and versatile activity for the brain, combining vocal-motor, auditory, linguistic, cognitive, emotional, and social brain processes, both in the left and right hemisphere. The capacity to sing is often preserved in aphasia after stroke, and singing-based methods, such as Melodic Intonation Therapy (MIT), can be effective in rehabilitating speech production in aphasics. Also emotionally and socially, singing could provide a powerful alternative channel for aphasic patients to express their emotions and interact with others, but the communal or group-level use of singing in aphasia rehabilitation has not been systematically studied.

AIMS: The purpose of the study is to determine the clinical and neural efficacy of a novel choir singing intervention in subacute/chronic aphasia. Specifically, the targeted outcomes are (i) verbal and vocal-motor skills, (ii) cognitive skills, (iii) emotional functioning and quality of life, (iv) caregiver psychological well-being, and (v) structural and functional neuroplasticity. In addition, the capacity of singing and music learning in aphasia is explored.

METHODS: Subjects are 60 stroke patients with at least minor aphasia (≥ 6 months post-stroke) and their family members (FMs, N = 60) from Helsinki area recruited to a cross-over RCT study. Participants are randomized to two groups [N = 60 in both (30 patients, 30 FMs)], which receive a 16-week choir intervention either during the first (AB group) or second (BA group) half of the follow-up. The intervention is a combination of group training, which utilizes a novel combination of traditional senior choir singing and MIT-like speech training protocols, and home training in which the choir material is trained with a tablet computer. All patients are evaluated at baseline, 5-month, and 9-month stages with language, cognitive, and auditory-music tests and questionnaires. Half of the patients (N = 30) also undergo electroencephalography (EEG) and structural and functional magnetic resonance imaging (s/fMRI). FMs are evaluated with questionnaires.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

The following inclusion criteria are used in patient recruiment:

  1. age over 18
  2. Finnish-speaking
  3. time since stroke > 6 months
  4. at least minor non-fluent aphasia due to stroke (BDAE Aphasia Severity Rating scale score ≤ 4)
  5. no hearing deficit
  6. no severe cognitive impairment affecting comprehension (the patient is able to understand the purpose of the study and give an informed consent)
  7. no neurological / psychiatric co-morbidity or substance abuse
  8. ability to produce vocal sound (through singing or humming).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

100 participants in 2 patient groups

Early singing intervention (AB)
Experimental group
Description:
Participants receive a 16 weeks of singing-based rehabilitation and standard care (SC) followed by 16 weeks of SC only.
Treatment:
Behavioral: Singing-based rehabilitation
Other: Standard care
Late singing intervention (BA)
Experimental group
Description:
Participants receive a 16 weeks of SC only followed by 16 weeks of singing intervention and SC.
Treatment:
Behavioral: Singing-based rehabilitation
Other: Standard care

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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