Swallowing study pulled before it began: remote monitoring idea never tested
NCT ID NCT04969874
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to see if monthly video calls could help track swallowing issues in people who had intensive rehab after throat cancer treatment. It planned to enroll adults with chronic swallowing problems and check if they could attend at least 3 out of 5 remote sessions. However, the trial was withdrawn before any participants were enrolled, so no results are available.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Started
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Jan 2021
- Finished
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May 2026
- 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.
- Ages
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18 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient aged 18 or over and treated for cancer of the upper aero-digestive tract: * Patient having spent a stay at the intensive rehabilitation center for laryngectomees * Patient with a medical diagnosis of swallowing disorders at risk of inhalation * Patient having the possibility of accessing a device allowing the use of the software by video (smartphone, tablet and / or computer) * Informed consent signed by the patient. * Patient affiliated to a social security scheme or equivalent Exclusion Criteria: * Progressive neurological disease leading to cognitive disorders * Patient with guardianship, curators or legal protection * Inability to give consent * Patient participating in another research including an exclusion period still in progress * Patient with speech therapy whose frequency is greater than 1 weekly session
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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.
Contacts and locations
Locations
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CHU Toulouse
Toulouse, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.