Support groups for patients who have had a laryngectomy
Workshops and Exchange Groups for Laryngectomized Patients
This study is testing whether support groups can help people who have had their voice box removed due to cancer feel better and improve their quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris) |
| Trial ID | NCT06077643 on ClinicalTrials.gov |
What this trial studies
This observational study aims to improve the quality of life for patients who have undergone total laryngectomy due to laryngeal cancer. It involves creating self-help and support groups where participants can share experiences and receive guidance from resource patients. The sessions will include presentations, discussions with experts, and assessments of patient satisfaction using quality of life questionnaires. The study focuses on addressing the psychological and social challenges faced by laryngectomized patients post-surgery.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 who have had a total laryngectomy within the last four years and can attend all sessions at Bichat Hospital.
Not a fit: Patients who are bedridden for more than 50% of the time or do not speak or understand French may not benefit from this study.
Why it matters
Potential benefit: If successful, this initiative could significantly enhance the emotional and social well-being of laryngectomized patients.
How similar studies have performed: While there is limited research specifically on support groups for laryngectomized patients, similar approaches in other cancer care contexts have shown positive outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Paris
- Bichat - Claude Bernard Hospital — Paris, France (Recruiting)
Study contacts
- Principal investigator: Angèle Germon — Assistance Publique - Hôpitaux de Paris
- Study coordinator: Angèle Germon
- Email: angele.germon@aphp.fr
- Phone: 06.40.65.58.75
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.