Evaluation of the Interest of a Video-assisted Remote Speech Therapy Consultation in Patients With ORL Cancer (TELE ORTHOPHONIE)

  • End date
    Jun 9, 2024
  • participants needed
  • sponsor
    Institut Claudius Regaud
Updated on 4 October 2022


Interventional, prospective, single-centre study aimed to evaluate the impact of a video-assisted remote speech therapy consultation in relation to the complexity and specificity of the care of patients with ORL cancer. Three indications will be studied: phonation problems, swallowing problems and other problems.

The study will be conducted on a population of patients with T3, T4 ORL cancer requiring speech therapy.

Each patient included will have a video-assisted speech therapy consultation with a private speech therapist and an expert speech therapist. At the end of this video consultation, the patient and the private speech therapist will be asked to complete a satisfaction questionnaire.

At the follow-up visit following the video-assisted consultation, the patient will have completed participation in the study.

Condition ORL Cancer
Treatment Patient managed at the IUCT-O and by a private speech therapist (near the patient's home).
Clinical Study IdentifierNCT04940000
SponsorInstitut Claudius Regaud
Last Modified on4 October 2022


Yes No Not Sure

Inclusion Criteria

Age ≥ 18 years at study entry
Patient with T3-T4 carcinological pathology of the VADS, relevant to surgery and/or radiotherapy and/or chemotherapy
Patient managed at the IUCT-O and by a private speech therapist (near the patient's home)
Patient affiliated to a Social Security system in France
Patient having signed informed consent prior to inclusion in the study and prior to any specific study procedure

Exclusion Criteria

Pregnant or lactating women
Any psychological, familial, geographical or sociological condition that does not allow for compliance with the medical follow-up and/or procedures foreseen in the study protocol
Patients deprived of their liberty or under legal protection (guardianship and tutorship, safeguard of justice)
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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