Cognitive Functioning in People With Myasthenia Graivs: Impact on Daily Life Activities, Work, Disability and Quality of Life
MYCOG
1 other identifier
observational
150
1 country
1
Brief Summary
MYCOG primarily aims to estimate the prevalence of cognitive difficulties in patients with MG treated at Besta Institute. Secondary aims include: a) assess the degree to which cognitive difficulties are associated to work impairment, limitations in ADL, symptoms of anxiety and depression, fatigue, disability and QoL; b) assess whether patients with different MG types show different degrees of cognitive impairment; c) assess whether patients with different MG antibody profiles show different degrees of cognitive impairment; d) assess whether patients under different MG-specific pharmacological treatments show different degrees of cognitive impairment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jun 2023
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 7, 2023
CompletedFirst Submitted
Initial submission to the registry
December 2, 2024
CompletedFirst Posted
Study publicly available on registry
December 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 12, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2025
CompletedFebruary 19, 2026
February 1, 2026
2.2 years
December 2, 2024
February 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
GEMS
Global examination of cognitive functioning
22 months
Secondary Outcomes (10)
CRIq
22 months
ENB-3
22 months
MG-DIS
22 months
MG-QOL15
22 months
MG-ADL
22 months
- +5 more secondary outcomes
Eligibility Criteria
Italian speakers, already followed at Besta Institute
You may qualify if:
- Patients with MG,
- followed-up at Besta institute
- aged 18-99,
- able to understand Italian language;
You may not qualify if:
- psychiatric comorbidies of psychotic nature;
- do not accept to participate on a voluntary basis;
- patients who should be excluded based on physician's judgement;
- patients who live in a nursing home for aged or disabled persons;
- respiratory impairment (patients under mechanical ventilation)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Fondazione IRCCS Istituto Neurologico Carlo Besta
Milan, 20133, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 2, 2024
First Posted
December 5, 2024
Study Start
June 7, 2023
Primary Completion
August 12, 2025
Study Completion
September 30, 2025
Last Updated
February 19, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share