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Study of Mental Fatigue in Polio Survivors

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00487487
Enrollment
Unknown
Registered
2007-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2007-06-18

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

Conditions

Post-Poliomyelitis Syndrome

Keywords

Candidates for this study are survivors of paralytic poliomyelitis

Brief summary

Post-Poliomyelitis Syndrome (PPS) is the term describing the new problems affecting polio survivors many years after recovery from paralytic polio. Among the symptoms, fatigue is one of the most frequent and debilitating. In addition to physical incapacitation, the fatigue of PPS also affects mental function. The term brain fatigue is usually used by patients to express problems on the areas of attention, concentration, memory and clear thinking. Unfortunately, little is known about cognitive fatigue of PPS patients. This study is meant to examine if mental impairment is present in PPS patients and, if so, how it interferes on the self-function of patients. Patients will undergo an interview, clinical and neurological evaluation, and a battery of screening laboratory tests to make sure they are eligible for the study. Patients who qualify will undergo neuropsychometric tests in order to assay performance in the main areas of cognitive functioning. Through this organized approach we expect to be able to determine if mental fatigue is a significant problem affecting polio survivors, what areas are most affected, and how it may interfere with daily living.

Interventions

None listed

Sponsors

Uniformed Services University of the Health Sciences
Lead SponsorFED

Study design

Time perspective
OTHER

Eligibility

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

Inclusion criteria

* 18 years of age or older * Be a survivor of poliomyelitis * Willing to attend two clinic visits for completion of screening procedures and required tests

Exclusion criteria

* Suffer from medical conditions that can interfere with cognitive function, including stroke, traumatic brain injury, dementia (progressive memory loss), severe depression, psychosis or other psychiatric disorders, etc.

Countries

United States

Contacts

Primary ContactSandra Maxwell, RN
smaxwell@usuhs.edu301-9840400

Outcome results

None listed

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