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

I

Institut Claudius Regaud

Status

Enrolling

Conditions

ORL Cancer

Treatments

Other: Patient managed at the IUCT-O and by a private speech therapist (near the patient's home).

Study type

Interventional

Funder types

Other

Identifiers

NCT04940000
21VADS03

Details and patient eligibility

About

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.

Enrollment

105 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  1. Pregnant or lactating women.
  2. 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.
  3. Patients deprived of their liberty or under legal protection (guardianship and tutorship, safeguard of justice).

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

105 participants in 1 patient group

Patient with T3-T4 ORL cancer, relevant to surgery and/or radiotherapy and/or chemotherapy.
Experimental group
Treatment:
Other: Patient managed at the IUCT-O and by a private speech therapist (near the patient's home).

Trial contacts and locations

1

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Central trial contact

Jérôme SARINI; Jean-Claude FARENC

Data sourced from clinicaltrials.gov

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