Blumenfeld 2012.
Methods | Parallel‐group randomised controlled trial |
Participants | Inclusion criteria: people with a tracheostomy, naive to a speaking valve, and with dysphagia. |
Interventions |
Intervention Received a speaking valve used for 45 minutes/day and during therapy. Control Received an inner cannula only. |
Outcomes |
|
Notes | Unable to identify published study. |