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Long term follow-up of PLS-patients: cognitive aspects and reliability of the diagnose

Long term follow-up of PLS-patients: cognitive aspects and reliability of the diagnose - Long term follow-up of PLS-patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43298
Enrollment
55
Registered
2016-06-15
Start date
2016-08-04
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

PLS Primary lateral sclerosis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Participation of the former PLS related study of 2003-2006 Age 18-years or above.

Exclusion criteria

Exclusion criteria: None.

Design outcomes

Primary

MeasureTime frame
Reliability of the diagnose will be tested by use of anamnesis, neurological examination and genetic research. Cognitive and behavioural functioning will be assessed and explored using the ECAS, ALS-FTD-Q, FAB and HADS rating scales. Neuropsychological evaluation will be performed.

Secondary

MeasureTime frame
Physical deterioration and functioning of the patient will be measured by use of the MRC-scores used during the neurological investigation and the ALS-FRS scale.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)