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

  • Age ≥ 18 years at study entry.
  • Patient with 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).

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

Jean-Claude FARENC; Jérôme SARINI

Data sourced from clinicaltrials.gov

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