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Assessment Effectiveness of the Leap Motion Capture® System on the Functionality of the Upper Limb in Acquired Brain Injury

Assessment Effectiveness of the Leap Motion Capture® System on the Functionality of the Upper Limb in Acquired Brain Injury

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04166617
Enrollment
30
Registered
2019-11-18
Start date
2019-11-12
Completion date
2021-11-11
Last updated
2019-11-18

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

Conditions

Brain Injuries, Traumatic, Patient Satisfaction, Stroke, Treatment Adherence

Brief summary

The affectedness of the motor control of the upper limb, particulary, the hand and/or fingers, appears in many neurological diseases, what is going to impact on the functionality of the subject. The use of new technologies in the rehabilitation environment, has the target to reduce the impact on the disabling conditions. So that, the goal of this investigation is to evaluate the system use effectiveness of the Leap Motion Controller® in the treatment on the upper limb on patients with neurological disease.

Interventions

OTHERConventional therapy

conventional physcial therapy rehabilitation for the upper limb

OTHERLeap motion plus conventional therapya

leap motion plus conventional physcial therapy rehabilitation for the upper limb

Sponsors

Universidad Rey Juan Carlos
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

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

Inclusion criteria

* people aged between 30 and 70 years old; * with a confirmed diagnosis of brain damage (\>6 months); * UL motor impairment with a Fugl-Meyer score≥16; * a modified Ashworth scale score≤2 in the deltoid, triceps brachii, biceps brachii and in the wrist and finger flexor and extensor muscles of the upper limb

Exclusion criteria

* the inability to understand instructions and actively cooperate in the tasks indicated based on a score ≥ 24 in the Mini-mental Test; * refusal to participate in the study; * visual impairment not correctable by glasses.

Design outcomes

Primary

MeasureTime frameDescription
Action Research Arm Test (ARAT)8 weeksShoulder Pain - Physioplus Objective The Action Research Arm Test (ARAT) is a 19 item observational measure used by physical therapists and other health care professionals to assess upper extremity performance (coordination, dexterity and functioning)
Jamar8 weeksJamar® hydraulic hand dynamometer was used to measure grip strength.
Box and blocks8 weeksBox and Blocks Test (BBT) was performed to measure unilateral gross manual dexterity in both the less and more affected side.

Secondary

MeasureTime frameDescription
Adherence to the therapy sessions8 weeksthe attendance rate (%) for therapy sessions
Questionary of Patient Satifaction8 weekswhich evaluate the level of satisfaction regarding the care and quality of the service received and the level of fulfillment of the patient's expectations regarding the treatment administered

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026