Your personality might predict how well you learn to speak again after laryngectomy
NCT ID NCT06856863
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
After losing their voice box to cancer, some people learn to speak using their throat and esophagus (oroesophageal voice). This study looks at whether personality traits, measured by a questionnaire, are linked to success in learning this new voice. Researchers will study 40 adults who had a laryngectomy and compare personality profiles of those who learned well versus those who struggled.
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 could help speech therapists personalize training for patients learning oroesophageal voice after laryngectomy.
- What could go wrong
- This is a small, observational study (40 people) that only looks for a link, not a treatment. Results may not apply to everyone.
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
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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.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Oct 2028
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.
- Ages
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18 years and older
- 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.
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: * Men or women over 18 years of age * French-speaking patients * MoCA score ≥ 16/30 * Patients who have undergone laryngectomy or total pharyngo-laryngectomy between 6 months and 5 years of age * Patients who have agreed to learn VOO * Patients who began speech therapy to learn VOO no more than five years ago * Patients who have had access to speech therapy to learn VOO for at least six months (completed or ongoing) * Patients who have received information about the study and have not expressed their opposition * Patients who are beneficiaries of or entitled to social security coverage Exclusion Criteria: * Patients who underwent a laryngectomy or total pharyngolaryngectomy more than 5 years ago * Patients who did not receive speech therapy to learn OVO postoperatively, or who received less than 6 months of therapy * Patients with a related condition that prevents them from learning VOO (anatomical or physiological abnormality, esophageal stenosis) * Patients with a related condition that may be responsible for speech or fluency disorders (developmental, organic, or functional speech and language disorders, stuttering, stammering, fluency disorders, neurological speech disorders) * Patients with uncorrected hearing loss * Patients unable to receive informed consent about the ongoing research due to impaired psychological or physical health * MoCA score \<16/30 * Patients with definite depressive symptoms (HAD-D score ≥ 11) * Patients in a period of exclusion from another research protocol at the time of collection of the non-opposition. * Subjects covered by articles L1121-5 to 1121-8 of the French Public Health Code (minors, adults under guardianship or trusteeship, patients deprived of their liberty, pregnant or breast-feeding women, etc.).
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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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Assistance Publique Hopitaux de Marseille
RECRUITINGMarseille, 13005, France
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