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Support groups tested to boost quality of life for throat cancer survivors

NCT ID NCT06077643

Symptom relief Sponsor: Assistance Publique - Hôpitaux de Paris Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether workshops and exchange groups can improve quality of life for people who have had their larynx removed due to cancer. Researchers will compare quality-of-life scores between 50 participants who join the program and a control group. The goal is to see if group support helps patients cope better after surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
workshops and exchange groups
What this could lead to
If successful, this program could offer a simple, non-drug way to improve daily life and emotional well-being for people who have had their larynx removed.
What could go wrong
This is a small, early-stage study with only 50 participants. The program may not lead to lasting improvements, and results may not apply to all laryngectomy patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 50 people

The number the study aims to enrol. It can still change while the study runs.

Started

Oct 2023

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patient who has benefited from a total laryngectomy in the ENT department of Bichat Hospital or Georges Pompidou European Hospital, less than four years ago.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Have had a total laryngectomy at Bichat Hospital or HEGP within the last four years * Have completed all the specific care of the pathology that required the total laryngectomy * Be able to travel to Bichat Hospital for all four sessions * Be over 18 years of age * Have received informed information about the conduct of the research. Exclusion Criteria: * WHO simplified autonomy scale greater than 2, i.e. from normal activity to ambulant and able to take care of themselves, but unable to provide work and bedridden for less than 50% of their time * Patient who does not speak or understand French * Lack of affiliation to a social security scheme or CMU * Patient benefiting from legal protection measures (guardianship or curatorship) * Patient who has communicated an objection to their inclusion, after informed information.

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Conditions

The condition(s) this trial relates to.

laryngeal carcinoma laryngeal neoplasm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Laryngeal cancer Laryngectomy; status

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Bichat - Claude Bernard Hospital

    RECRUITING

    Paris, 75018, France

More trials for these conditions

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