WithdrawnNot Applicable

Remote Orthophonic Follow-up on Patients With Chronic Swallowing Disorders

Stopped: Software problem

France0Started 2021-01-01

Plain-language summary

The study will assess the feasibility of monthly post rehabilitation remote monitoring, using the "MAX Educ" webvision app, in patients with sequelae of aerodigestive cancer treatments.

Who can participate

Age range

18 Years – 100 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patient aged 18 or over and treated for cancer of the upper aero-digestive tract: * Patient having spent a stay at the intensive rehabilitation center for laryngectomees * Patient with a medical diagnosis of swallowing disorders at risk of inhalation * Patient having the possibility of accessing a device allowing the use of the software by video (smartphone, tablet and / or computer) * Informed consent signed by the patient. * Patient affiliated to a social security scheme or equivalent Exclusion Criteria: * Progressive neurological disease leading to cognitive disorders * Patient with guardianship, curators or legal protection * Inability to give consent * Patient participating in another research including an exclusion period still in progress * Patient with speech therapy whose frequency is greater than 1 weekly session

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

patient attendance at monthly remote monitoring

Timeframe: Month 6 : end of follow-up

Trial details

NCT IDNCT04969874

SponsorUniversity Hospital, Toulouse

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-05-07

View on ClinicalTrials.gov More Deglutition trials

Who can participate

Age range

18 Years – 100 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.