RecruitingNot ApplicableNCT06368323

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


Sponsor

University of Ottawa

Enrollment

50 participants

Start Date

Apr 22, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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)


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • 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 Criteria6

  • 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

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALChoir singing

The 12-week intervention will consist of 12 in-person choir-singing sessions (1 session/week, 1,5 h/session, total 18h) conducted by a choir master in addition to home training (3 x 30-minutes-sessions/week, total 18h). In total, participants will undergo the intervention for 3 hours/week for 12 weeks (i.e., 36 hours).

OTHERUsual care

Rehabilitation services received by patients and social activities will be monitored and documented.


Locations(4)

University of South Florida

Tampa, Florida, United States

University of Ottawa

Ottawa, Ontario, Canada

Toronto Metropolitan University

Toronto, Ontario, Canada

Université de Montréal

Montreal, Quebec, Canada

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06368323


Related Trials