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Education Program in Myasthenia

Efficiency of a Therapeutic Patient Education Program in Myasthenia Gravis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04714658
Acronym
MG-ETP
Enrollment
100
Registered
2021-01-19
Start date
2021-01-22
Completion date
2025-05-22
Last updated
2021-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Auto-immune Myasthenia

Brief summary

Patient therapeutic education (PTE) has become a must in the modern management of chronic diseases. Its main objective is to improve compliance with treatment and the application of preventive measures. The main goal of this study is to assess the influence of the therapeutic education program on the perception of the disease in patients with autoimmune myasthenia. Secondary objectives are to assess quality of life, patient satisfaction of the PTE program, the acquisition of therapeutic goals and the influence of therapeutic education on the evolution of autoimmune myasthenia Study team hypothesize that therapeutic education could improve the patient's perception of myasthenia and its quality of life. By improving patient's adherence to treatments and his knowledge of the disease, it could also improve the evolution of myasthenia gravis. Study team suppose that PTE program can reduce the absenteeism at work, the number and duration of hospitalizations, particularly those in intensive care units.

Interventions

OTHERTherapeutic Education

Each patient will participate in 1 to 3 PTE sessions. 1. st group collective workshop : allow the patient to better understand autoimmune 2. nd workshop : fatigue and techniques that enable its best management. 3. rd workshop : improving the management of the emotions generated by myasthenia. It allows patients to express their experiences of the disease in front of a group, to talk about their difficulties in their relationships and mobilize their resources to promote exchanges.

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient with generalized autoimmune myasthenia with Acetylcholine Receptor Antibodies (AChR Ab) or with antibodies to the muscle-specific receptor tyrosine kinase (MuSK Ab) * Patient agreeing to participate in the therapeutic education program * Signing consent * Subject affiliated with a health insurance social protection regiment

Exclusion criteria

* Patients without serological confirmation of myasthenia or pure ocular form * Patient with cognitive impairment or behavioral problems that, in the investigator's opinion, will compromise their ability to comply with study procedures * Refusal of the patient to participate in the study * Patient who has already benefited from the therapeutic education program in myasthenia * Age \< 18 y.o. * Subject under safeguarding justice * Subject under guardianship or under curatorship

Design outcomes

Primary

MeasureTime frame
Brief Illness Perception Questionnaire6 month after the first visit

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026