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Trial Title: Articulatory Adaptation Following Oral Cancer Treatment

NCT ID: NCT05876247

Condition: Oral Cavity Squamous Cell Carcinoma
Speech Disorders

Conditions: Official terms:
Mouth Neoplasms
Squamous Cell Carcinoma of Head and Neck
Speech Disorders

Conditions: Keywords:
Articulation

Study type: Observational

Overall status: Recruiting

Study design:

Time perspective: Prospective

Intervention:

Intervention type: Other
Intervention name: Electromagnetic Articulography
Description: Motion tracking sensors will track articulatory movements of the tongue, jaw and lips
Arm group label: Control speakers
Arm group label: Individuals treated for oral cancer

Summary: The goal of this longitudinal study is to learn more about the articulatory consequences of surgical oral cancer treatment. The main aims are to study the coordination and development of speech articulation of patients who will undergo surgical treatment for oral cancer longitudinally and whether individual differences in the reliance on auditory or tactile information can predict the success of speech compensatory strategies. Participants will perform multiple speech tasks while motion tracking sensors track the articulatory gestures.

Criteria for eligibility:

Study pop:
Adults with and without oral cancer who speak Dutch as their native language

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: 1. Diagnosed with T1 or T2 tumor in the oral cavity 2. At least 18 years old and able to provide informed consent 3. Native speaker of Dutch 4. Has nog been treated for oral cancer before Exclusion Criteria: 1a. Recurrence of disease (for patients) 1b. Treated for oral cancer (for healthy controls) 2. Speech problems (e.g., stuttering) 3. Problems with sight or hearing that impede reading or understanding instructions. When glasses or a hearing aid resolve these problems, then participants are not excluded. 4. Neurological or psychological disorders (e.g., stroke) 5. Non-removable metal in, on or around the head (piercings, braces, pacemaker, electrodes) 6. Self-reported signs of depression

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: Accepts Healthy Volunteers

Locations:

Facility:
Name: Faculty of Arts, University of Groningen

Address:
City: Groningen
Zip: 9712 EK
Country: Netherlands

Status: Recruiting

Contact:
Last name: Thomas Tienkamp, MA

Phone: +31 50 36 37051
Email: t.b.tienkamp@rug.nl

Facility:
Name: University Medical Centre Groningen

Address:
City: Groningen
Zip: 9713 GZ
Country: Netherlands

Status: Recruiting

Contact:
Last name: Thomas Tienkamp, MA

Phone: +31 50 36 37051
Email: t.b.tienkamp@umcg.nl

Start date: November 10, 2022

Completion date: August 2025

Lead sponsor:
Agency: University Medical Center Groningen
Agency class: Other

Source: University Medical Center Groningen

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05876247

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