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Effect of Community Choir Singing in People With Chronic Post-stroke Aphasia

Aphasia

The goal of this randomized controled trial is to test the effects of assigning people with chronic post-stroke aphasia to 12 weekly choir sessions, compared to usual care.

The main question it aims to answer is:

Does the assignment to a choir singing program causes a beneficial effect on functional communication and language recovery as well as psychosocial outcomes compared to usual care in the rehabilitation of people with chronic post-stroke aphasia?

Participants will have:

12 in-person choir-singing sessions (1 session/week, 1,5 h/session, total 18h) conducted by a choir master, and home singing training (3 x 30-minutes-sessions/week, total 18h)

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* People with chronic aphasia following stroke
* English or French as language of daily use
* Last stroke must have occurred at least 6 months before the start of the first assessments in the study protocol.

Exclusion Criteria:

* Regular music making in the past 6 months
* Visual deficit that cannot be corrected and might impair testing
* Hearing deficit that cannot be corrected and might impair testing
* Presence of neurological/psychiatric co-morbidity or substance abuse
* No ability to produce vocal sound through singing/humming
* Legally considered unable to make decisions for oneself

Study Location

University of Ottawa
University of Ottawa
Ottawa, Ontario
Canada

Contact Study Team

Primary Contact

Anna Zumbansen, PhD

[email protected]
613-562-5800
Backup Contact

Narges Bayat, Master

[email protected]
613-562-5800
Toronto Metropolitan University
Toronto Metropolitan University
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Arla Good, Ph.D.

[email protected]
Université de Montréal
Université de Montréal
Montréal, Quebec
Canada

Contact Study Team

Primary Contact

Carole Anglade, Ph.D.

[email protected]
Study Sponsored By
University of Ottawa
Participants Required
More Information
Study ID: NCT06368323