Can new tools help ICU patients who cannot speak?
NCT ID NCT07796035
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
This study explores the communication challenges faced by healthcare providers when caring for non-verbal patients in intensive care, such as those with spinal cord injury or a tracheostomy. Researchers will interview nurses and speech-language pathologists, then survey a larger group to identify the most important communication needs and the limits of current methods. The goal is to inform the development of practical communication tools for acute care settings.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could guide the design of better communication tools for non-verbal patients in intensive care, potentially reducing distress and improving care.
- What could go wrong
- This is an early-stage needs assessment with a small sample, so findings may not apply to all settings. The study does not test any communication tool directly.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Care givers to the non-verbal patients with communication barrier
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * be a healthcare provider such as physicians, registered nurses, speech-language pathologists, occupational therapists, or physiotherapists; * work in ICU, spine, neurosurgical, or related acute care inpatient settings; * have experience caring for patients with impaired verbal communication, including patients with tracheostomy, mechanical ventilation, or spinal cord injury; and * be able to provide informed consent. A small subset of family caregivers may also be included if they have direct experience supporting communication for patients with impaired verbal communication in these settings. Exclusion Criteria: * Individuals not directly involved in the care of patients with impaired verbal communication in the relevant clinical settings * Trainees who are not yet independently practicing, unless they are participating in an independent clinical role * Family caregivers without direct experience supporting communication needs in the acute care setting
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Vancouver General Hospital
Vancouver, British Columbia, V5Z 1M9, Canada
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Other studies related to the condition(s) this trial covers.
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