Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT05621889

Innovative Patient-partner-guided Virtual Group Speech Pathology Intervention Model in Head and Neck Cancer

Led by Centre hospitalier de l'Université de Montréal (CHUM) · Updated on 2025-03-21

76

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

Sponsors

C

Centre hospitalier de l'Université de Montréal (CHUM)

Lead Sponsor

U

Université du Québec à Trois-Rivières

Collaborating Sponsor

AI-Summary

What this Trial Is About

This project aims to study an innovative intervention, the eG2 Intervention, developed by speech-language pathologists at the Centre hospitalier de l'Université de Montréal to improve therapeutic adherence and prevent dysphagia in patients treated with chemoradiotherapy for head and neck cancer. The innovation consists in offering a speech therapy intervention that is 1) virtual, 2) group-based (whereas it is usually individual) and 3) involves a patient partner. This intervention has the potential to improve quality of care, accessibility to services and optimize health care resources.

CONDITIONS

Official Title

Innovative Patient-partner-guided Virtual Group Speech Pathology Intervention Model in Head and Neck Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 60 18 years of age with a diagnosis of head or neck cancer
  • Chemoradiotherapy treatments planned for curative purposes
  • Planned external radiation therapy dose of at least 60 60 Grays
  • Sufficient proficiency in French to complete self-reported questionnaires
Not Eligible

You will not qualify if you...

  • Remote metastases
  • Previous or planned total laryngectomy
  • Previous moderate or severe dysphagia known and/or evaluated by speech therapy
  • Diagnosis of a second synchronous cancer at the time of study enrollment
  • History of prior radiation therapy to the head and neck area
  • Cognitive impairment (diagnosed or suspected) that may interfere with participation and measurements

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier de l'Université de Montréal

Montreal, Quebec, Canada, H2x 3E4

Actively Recruiting

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Research Team

M

Marie-Eve Caty, M.P.O., Ph.D.

CONTACT

H

Houda Bahig, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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