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CompletedNCT07928050Updated Nov 10, 2026

RehaBEElitation - Serious Game-Based Experimental Protocol to Improve Manual Dexterity in Individuals With Parkinson's Disease

An interventional study of RehaBEElitation serious game and Home exercise booklet in Parkinson Disease, sponsored by Federal University of Uberlandia. Completed at 1 site in Brazil. Open to participants aged 40 Years to 100 Years. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Federal University of Uberlandia · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 11 months after the study started (first participant enrolled Oct 2023, registered Oct 2026).
Updated Nov 10, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
27
Allocation
Non-randomized
Ages
40 Years to 100 Years
Sex
All
01

Study summary

This is a non-randomized controlled trial with two parallel groups, with the general objective of developing and applying an assessment and intervention protocol based on a serious game for the rehabilitation of hand function in individuals with Parkinson's disease (PD). The experimental group trained with the RehaBEElitation serious game, controlled by hand and wrist movements through a wearable sensor glove; the control group trained the same five movements with a home exercise booklet. Both groups trained twice a week for six weeks (12 sessions of 30 to 45 minutes) and kept their usual physiotherapy. Participants were allocated in sequence: those enrolled first received the serious game and those enrolled later received the booklet. Manual dexterity, motor signs, quality of life, functioning and upper-limb muscle activation (surface electromyography) were assessed before and after the intervention. This trial was registered retrospectively.

02

Conditions studied

  • Parkinson Disease

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Keywords

  • Parkinson's disease
  • serious game
  • rehabilitation
  • manual dexterity
  • upper limb
  • electromyography
  • home exercise
03

In context

Parkinson Disease

4,573 studies on the registry are indexed under Parkinson Disease; 1,086 are open to participants now.

This study's enrollment of 27 is below the median of 40 across 3,353 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

Federal University of Uberlandia is the lead sponsor of 61 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Diagnosis of Parkinson's disease confirmed by a neurologist or geriatrician
  • Age between 40 and 100 years
  • Mild to moderate disease (Hoehn \& Yahr stages I to III)
  • score above 25
  • No severe visual (Snellen chart) or hearing impairment
  • No other neurological or musculoskeletal disease
  • Functional and body-structure requirements for the training, assessed with the ICF checklist
  • Read and agreed to the form

Exclusion criteria

Exclusion Criteria:

  • Uncontrolled hypertension, unstable angina or recent myocardial infarction
  • History of seizures
  • Participation in another clinical trial involving rehabilitation or an experimental drug
  • Missing more than three sessions or withdrawing from the intervention
Terms in these criteria, in plain language(2)

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.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
27 participants (actual)

Study arms

  • Experimental
    RehaBEElitation serious game

    Group of subjects with Parkinson's disease trained with the RehaBEElitation serious game, twice a week for six weeks (12 sessions of 30 to 45 minutes), in addition to usual physiotherapy.

    Device: RehaBEElitation serious game

  • Active comparator
    Home exercise booklet

    Group of subjects with Parkinson's disease trained with a home exercise booklet with the same five movements, twice a week for six weeks (12 sessions of 30 to 45 minutes), with remote follow-up, in addition to usual physiotherapy.

    Behavioral: Home exercise booklet

Interventions

  • DeviceRehaBEElitation serious game

    3D serious game controlled by hand and wrist movements (open/close the hand, pinch grip, wrist flexion-extension and radial-ulnar deviation, forearm pronation-supination) through a wearable glove with inertial and force sensors and haptic feedback. Twice a week for six weeks (12 sessions of 30 to 45 minutes).

  • BehavioralHome exercise booklet

    Printed booklet with the same five hand and wrist movements, performed in two sets of 2 minutes with 1 minute of rest, twice a week for six weeks (12 sessions of 30 to 45 minutes), with remote follow-up.

06

What researchers measure

Primary outcomes

  1. Box and Block Test

    Number of blocks transferred in 60 seconds with the most affected hand. Higher scores mean a better outcome.

    Time frame: Baseline and 6 weeks

  2. Nine-Hole Peg Test

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

    Time frame: Baseline and 6 weeks

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

    Clinical scale of motor signs. Each item is rated from 0 (normal) to 4 (severe); higher scores mean a worse outcome.

    Time frame: Baseline and 6 weeks

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

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

    Time frame: Baseline and 6 weeks

  5. International Classification of Functioning, Disability and Health (ICF) checklist

    Activity and participation components; functioning and disability in daily life.

    Time frame: Baseline and 6 weeks

  6. Muscle activation of the flexor carpi radialis (surface electromyography)

    EMG of the flexor carpi radialis, normalised to the maximal voluntary contraction (%MVC), averaged across the reaching task, the Box and Block Test, the Nine-Hole Peg Test and the Trail Making Test.

    Time frame: Baseline and 6 weeks

  7. Muscle activation of the extensor carpi ulnaris (surface electromyography)

    EMG of the extensor carpi ulnaris, normalised to the maximal voluntary contraction (%MVC), averaged across the reaching task, the Box and Block Test, the Nine-Hole Peg Test and the Trail Making Test.

    Time frame: Baseline and 6 weeks

  8. Muscle activation of the biceps brachii (surface electromyography)

    EMG of the biceps brachii, normalised to the maximal voluntary contraction (%MVC), averaged across the reaching task, the Box and Block Test, the Nine-Hole Peg Test and the Trail Making Test.

    Time frame: Baseline and 6 weeks

  9. Muscle activation of the triceps brachii (surface electromyography)

    EMG of the triceps brachii, normalised to the maximal voluntary contraction (%MVC), averaged across the reaching task, the Box and Block Test, the Nine-Hole Peg Test and the Trail Making Test.

    Time frame: Baseline and 6 weeks

  10. Muscle activation of the anterior deltoid (surface electromyography)

    EMG of the anterior deltoid, normalised to the maximal voluntary contraction (%MVC), averaged across the reaching task, the Box and Block Test, the Nine-Hole Peg Test and the Trail Making Test.

    Time frame: Baseline and 6 weeks

  11. Trail Making Test part A

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

    Time frame: Baseline and 6 weeks

  12. Trail Making Test part B

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

    Time frame: Baseline and 6 weeks

  13. Handwriting movement analysis

    Spiral and sinusoid drawings (10 copies of each).

    Time frame: Baseline and 6 weeks

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

  • Cardoso Mendes L, Abreu Rosa de Sa A, Alves Marques I, Morere Y, de Oliveira Andrade A. RehaBEElitation: the architecture and organization of a serious game to evaluate motor signs in Parkinson's disease. PeerJ Comput Sci. 2023 Mar 15;9:e1267. doi: 10.7717/peerj-cs.1267. eCollection 2023. PubMed 37346638 ↗

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.

Data sharing details ↗ · zenodo.org

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 10, 2026
Show all 1 update
  1. Nov 10, 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
NCT07928050
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 10, 2026
Start date
Oct 24, 2023
Primary completion
Nov 5, 2024
Completion
Nov 5, 2024
Last update
Nov 10, 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 ↗

Not currently enrolling

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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