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Could a special cushion improve swallowing? new study tests a simple device
NCT ID NCT02457052
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a portable sitting device (DATP) designed to improve posture and swallowing in people with swallowing disorders. 64 participants were randomly assigned to use the device or not, and their swallowing was measured after one month. The goal was to see if better sitting position could help with swallowing safety and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a portable custom sitting device (DATP) placed on a standard chair
- What this could lead to
- If it works, this could offer a simple, low-cost way to improve swallowing safety for people with swallowing disorders.
- What could go wrong
- This is a small, early-stage trial with only 64 participants. The device may not show meaningful improvement, and results may not apply to everyone with swallowing problems.
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.
- Phase
-
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.
- Participants
-
64 people
The number who actually took part.
- Start date
-
Oct 2014
- Finished
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Mar 2018
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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 : * Present a swallowing disorder authenticated by a score Dysphagia Handicap Index above 11 * Postural disorder authenticated by a score greater than 0 to at least 1 of the following 3 items to MCPAA: retroversion, obliquity and rotation of the pelvis * Autonomy Conservation compatible with the use of different seats including standard seats * Signing of informed consent Exclusion Criteria: * Postural disorder requiring the use of only one type of installation (wheelchair or hull) * Spinal stiffness or non-reducible hips (spondylitis, osteosynthesis rod) * Not included anthropometric dimensions between: * Basin with between 39 and 50 cm * femoral length between 42 and 52 cm * tibial length between 39 and 44 cm (46.5 with femoral recharge), measured with the shoes. * Pregnant or lactating women
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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
-
University Hospital, Toulouse
Toulouse, Midi-Pyrénées, 31059, France
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Other studies related to the condition(s) this trial covers.
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