ClinicalTrials.gg
CompletedNCT07931677Updated Nov 12, 2026

Identification of Cognitive and Motor Changes in Individuals With and Without Parkinson's Disease Using Hemoencephalography

An observational study in Parkinson Disease, sponsored by Federal University of Uberlandia. Completed at 1 site in Brazil. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-12.

Sponsored by Federal University of Uberlandia · Observational

Updated Nov 12, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
46
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 103 studies in Parkinson Disease with a site in Brazil — 19 open to participants now, 22 under way, 1 of them phase 3. Parkinson Disease · Brazil.

Started
2023
with 8 others
Observational
8 of 103
2 open now
Registered
100th of 103
by date
Lead sponsor
3 of 103
Federal University of Uberlandia

Among the 103 studies in Parkinson Disease with a site in Brazil, this one is one of 9 that started in 2023, is one of 8 observational ones, and was the 100th registered.

Parkinson Disease

4,576 studies on the registry are indexed under Parkinson Disease; 1,087 are open to participants now.

Browse Parkinson Disease studies →

Open to participants now

19 of the 103 studies in Parkinson Disease with a site in Brazil are open now. Recruiting first, the newest first:

14 more — sign in →

All 19 open studies →

A study can be open while its sites in Brazil have not opened yet or have stopped. Only those recruiting at a site in Brazil →

Who these studies take

Of the 749 Parkinson Disease studies recruiting now, 311 (42%) set no upper age limit and 127 (17%) stop at 75 or younger; 64 take children under 18; 189 take healthy volunteers.

This study: 18 Years and older · all sexes · healthy volunteers too.

The full table on the hub →

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 103 studies in Parkinson Disease with a site in Brazil, or all of them as a file.
02

Study summary

This is an observational, longitudinal study with a control group, with the general objective of analysing the pattern of response of prefrontal cortex activity during motor and cognitive tasks in individuals with and without Parkinson's disease (PD) over 12 months. Prefrontal activity was recorded with a portable hemoencephalography (HEG) device placed on the forehead, in rest-task-rest blocks, while participants performed the Box and Block Test, the Nine-Hole Peg Test, the Trail Making Test (parts A and B) and spiral and sinusoid drawings. The assessments were repeated in up to 12 sessions, planned approximately monthly, and the tasks were video-recorded showing only the hands. Participants with PD were also assessed with the MDS-UPDRS Part III, the Hoehn \& Yahr scale and the PDQ-39 at the first and last sessions. Information that can identify the participants will be removed from the database before storage in a repository. The results will contribute to understanding how prefrontal activity relates to motor and cognitive performance in PD and how it changes over time.

03

Conditions studied

  • Parkinson Disease

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Keywords

  • Parkinson's disease
  • hemoencephalography
  • prefrontal cortex
  • motor assessment
  • cognitive assessment
  • manual dexterity
  • longitudinal study
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

  • Experimental group: Individuals diagnosed with Parkinson's disease
  • Control group: Individuals without Parkinson's disease (PD) or other neurological disease

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Experimental group: diagnosis of Parkinson's disease
  • Experimental group: classified between stages 0 and 3 of the Hoehn \& Yahr scale
  • Experimental group: on antiparkinsonian medication
  • Both groups: no previous cardiorespiratory or musculoskeletal disorder

Exclusion criteria

Exclusion Criteria:

  • Use of deep brain stimulation
  • Visual impairment that affects the tests (Snellen \< 80)
  • below the education-adjusted cut-off (20 for 1-4 years of schooling, 25 for 5-8 years, 26.5 for 9-11 years and 29 for more than 11 years)
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

MMSE and MoCA

Short tests of memory and thinking, each scored out of 30. Lower scores suggest more difficulty; criteria give a range, either to include people with memory problems or to leave them out.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
46 participants (actual)
Patient registry
No

Groups and cohorts

  • Experimental group

    Group of subjects with Parkinson's disease

  • Control group

    Neurological healthy subjects

06

What researchers measure

Primary outcomes

  1. Prefrontal hemoencephalography during the Box and Block Test

    Prefrontal HEG index (dimensionless value reported by the device; no physical unit), expressed as the change from rest to task.

    Time frame: 12 months

  2. Prefrontal hemoencephalography during the Nine-Hole Peg Test

    Prefrontal HEG index (dimensionless value reported by the device; no physical unit), expressed as the change from rest to task.

    Time frame: 12 months

  3. Prefrontal hemoencephalography during the Trail Making Test part A

    Prefrontal HEG index (dimensionless value reported by the device; no physical unit), expressed as the change from rest to task.

    Time frame: 12 months

  4. Prefrontal hemoencephalography during the Trail Making Test part B

    Prefrontal HEG index (dimensionless value reported by the device; no physical unit), expressed as the change from rest to task.

    Time frame: 12 months

  5. Prefrontal hemoencephalography during spiral and sinusoid drawing

    Prefrontal HEG index (dimensionless value reported by the device; no physical unit), expressed as the change from rest to task.

    Time frame: 12 months

  6. Box and Block Test

    Number of blocks transferred in 60 seconds. Higher scores mean a better outcome.

    Time frame: 12 months

  7. Nine-Hole Peg Test

    Time in seconds to place and remove nine pegs. Higher values mean a worse outcome.

    Time frame: 12 months

  8. Trail Making Test part A

    Time in seconds to complete part A. Higher values mean a worse outcome.

    Time frame: 12 months

  9. Trail Making Test part B

    Time in seconds to complete part B. Higher values mean a worse outcome.

    Time frame: 12 months

  10. Pen speed during drawing

    Pen speed during spiral and sinusoid drawings, measured from the task videos, in percentage of the sheet size per second.

    Time frame: 12 months

  11. Drawing duration

    Time in seconds to complete the spiral and sinusoid drawings, measured from the task videos.

    Time frame: 12 months

  12. Drawing smoothness (spectral arc length)

    Spectral arc length (SPARC) of the pen trajectory during spiral and sinusoid drawings, measured from the task videos. Dimensionless; more negative values indicate less smooth movement.

    Time frame: 12 months

  13. MDS-Unified Parkinson's Disease Rating Scale Part III (MDS-UPDRS III)

    Clinical scale of motor signs of Parkinson's disease, applied to the experimental group. Each item is rated from 0 (normal) to 4 (severe); higher scores mean a worse outcome.

    Time frame: First and last sessions (12 months)

  14. Hoehn & Yahr scale

    Stage of Parkinson's disease (1 to 5), applied to the experimental group. Higher stages mean a worse outcome.

    Time frame: First and last sessions (12 months)

  15. Parkinson's Disease Questionnaire (PDQ-39)

    Disease-specific quality of life, applied to the experimental group. Summary index from 0 to 100; higher scores mean a worse outcome.

    Time frame: First and last sessions (12 months)

  16. Cognition (Mini-Mental State Examination)

    Screening score from 0 to 30. Higher scores mean a better outcome.

    Time frame: Baseline

  17. Visual acuity

    Visual acuity measured with the Snellen test

    Time frame: Baseline

07

Study locations

1 site
  • Núcleo de Inovação e Avaliação Tecnológica em Saúde / Centre for Innovation and Technology Assessment in Health
    Uberlândia, Minas Gerais 38408-100, Brazil
08

References and documents

Publications

  • de Moura Neto E, Cabral AM, Alves CM, Luvizutto GJ, Nardo JRM, Mendes LC, de Oliveira Andrade A. Hemoencephalography Reveals Activity of the Prefrontal Cortex During Motor Coordination Tasks in Individuals with Parkinson's Disease. In: XXIX Brazilian Congress on Biomedical Engineering. IFMBE Proceedings. Springer; 2025. p. 911-920. doi: 10.1007/978-3-031-93646-3_94

Individual participant data

Plan to share: Yes — The data will be anonymised and stored in a safe and international platform (Zenodo - https://zenodo.org/communities/niats). Only data that cannot be used to identify the participants will be shared.

Supporting information: Study protocol, Statistical analysis plan, Analytic code

Time frame: Starting 6 months after publication

Access criteria: Researchers that wish to have access to the data can request access at https://zenodo.org/communities/niats. Access will be granted for research purposes under a data sharing agreement.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Oct 2023 to primary completion in Jan 2026, 26 months.

Of 379 non-industry observational studies under Parkinson Disease, half reached primary completion within 48 months of starting (the median), counting those still running; a quarter within 22 and three quarters within 133. This study's 26 months is below that.

Counting every sponsor, half of 439 studies reached it within 47 months; a quarter within 22 and three quarters within 114.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 18, 2026
First posted
Nov 12, 2026
StartActual
Oct 23, 2023
Primary completionActual
Jan 13, 2026
CompletionActual
Jan 13, 2026
Last update
Nov 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 12, 2026
Show all 1 update
  1. Nov 12, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07931677
Lead sponsor
Federal University of Uberlandia
Collaborators
Núcleo de Inovação e Avaliação Tecnológica em Saúde
Responsible party
Adriano de Oliveira Andrade (Professor, Federal University of Uberlandia) — Principal investigator
First posted
Nov 12, 2026
Start date
Oct 23, 2023
Primary completion
Jan 13, 2026
Completion
Jan 13, 2026
Last update
Nov 12, 2026

Study contacts

Adriano Andrade, PhD
principal investigator · Federal University of Uberlandia

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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