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NCT06856863: CoPerVOO

Correlation Between Personnality Traits and Ability to Learn Oroesophageal Voice

Recruiting now NA Last updated 4 December 2025
What this trial tests

NA trial testing Test of personality : questionnary in Laryngectomy in 40 participants. Currently enrolling.

Timeline
14 October 2025
Primary endpoint
14 October 2027
14 October 2028

Quick facts

Lead sponsorAssistance Publique Hopitaux De Marseille
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment40
Start date14 October 2025
Primary completion14 October 2027
Estimated completion14 October 2028
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Assistance Publique Hopitaux De Marseille — full company profile →

Who can join

18 and older, any sex, with Laryngectomy or Total Pharyngo-laryngectomy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

After total laryngectomy and loss of laryngeal phonation, the oro-oesophageal voice (VOO) is a communication option for the patient. It involves little financial outlay and, when mastered, ensures functional communication, but requires time-consuming speech therapy. VOO acquisition depends on a number of factors, including the patient's physiology, personality and socio-cultural environment. Several authors have suggested the influence of psychology on failure to learn VOO, but the studies found in the literature are old and did not use personality tests to objectivize this link through quantitative analysis. Today, the Temperament and Character Inventory (TCI-125) is a personality test used clinically and in research, and appreciated for the quantitative scores it provides. The aim of our study is to ascertain whether salient personality traits (as measured by the TCI) are common to patients who succeed in learning VOO, compared with those who do not. 40 subjects who underwent total laryngectomy and had access to speech therapy will be included in this study. A speech assessment with audio recording will be performed and acoustic measurements will be taken. Subjects will also take the TCI-125. Finally, a perceptual evaluation by a jury of experts will categorize the subjects as good or poor speakers. Inclusion period: 24 months Duration of subject participation: 1 day Total duration: 36 months

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Assistance Publique Hopitaux De Marseille trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06856863.

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