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NCT06368323Recruiting

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

Source: ClinicalTrials.gov · Last updated 17 Feb 2026

Brief summary (registry, in English)

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)

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
1 Apr 2024
Start date
22 Apr 2024
Primary completion date
30 Sept 2027
Lead sponsor
University of Ottawa
Diseases
Stroke
NCT number
NCT06368323

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 22 Apr 2024 to the primary completion date, 30 Sept 2027
  • 4 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of neurological/psychiatric co-morbidity or substance abuse

Other

  • 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
  • No ability to produce vocal sound through singing/humming
  • Legally considered unable to make decisions for oneself

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Université de Montréal
Coordinator of this site? Confirm its status
MontrealCanadaCompleted
University of Ottawa
Coordinator of this site? Confirm its status
OttawaCanadaCompleted
Toronto Metropolitan University
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting
University of South Florida
Coordinator of this site? Confirm its status
TampaUnited StatesNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.