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Validity and feasibility of the PortaLite fNIRS device to measure brain activity during walking while performing a cognitive dual task in elderly with Parkinson*s disease - a pilot study

Validity and feasibility of the PortaLite fNIRS device to measure brain activity during walking while performing a cognitive dual task in elderly with Parkinson*s disease - a pilot study - Use of fNIRS during dual task walking in elderly with Parkinson*s Disease.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37012
Enrollment
20
Registered
2012-08-16
Start date
2012-08-31
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Parkinson's Disease

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age 60-85 years Diagnosis Parkinson*s Disease UKBB Hoehn and Yahr stage II-III (on medication) 2 or more falls within the 6 months prior to the study Able to walk at least 5 minutes unassisted (walking aid allowed) Deep Brain Stimulation parameters and medication stable for at least one month

Exclusion criteria

Exclusion criteria: Psychiatric co-morbidities (e.g., major depression - DSM IV criteria) History of stroke, traumatic brain injury, brain tumor or other neurological disorders Acute lower back or lower extremity pain, musculoskeletal injuries, peripheral neuropathy which restricts gait Clinical diagnosis of dementia (e.g., Alzheimer*s disease, vascular dementia) Severe freezing precluding safe participation Unable to comply with testing protocol

Design outcomes

Primary

MeasureTime frame
The signal-to-noise ratio of the PortaLite.

Secondary

MeasureTime frame
Changes in OxyHb, DeoxyHb, and total Hb in µmol/L from baseline to mean maximum value of a certain task measured with fNIRS Subjective perceived exertion is measure with a questionnaire (Borg schaal RPE)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)