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Effectiveness of Leap Motion on hand function in children with cerebral palsy

Effectiveness of Leap Motion controller on the functionality of the upper limb in children with bilateral spastic cerebral palsy: Randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210616051599N2
Enrollment
20
Registered
2022-05-08
Start date
2022-05-26
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Cerebral palsy. Cerebral palsy

Interventions

Intervention 1: Intervention group: In this study, the intervention will be a clinical trial in two groups of intervention and control. At the beginning of the intervention phase, an assessment is mad

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 8 Years

Inclusion criteria

Inclusion criteria: Age category 5 to 8 years. Ability to understand and follow simple verbal commands. Diagnosis of bilateral spastic cerebral palsy by a neurologist based on medical records. Level one or two or three manual ability classification system. Level one or two or three systems of gross motor function. No history of Botox injections, surgery and upper limb fractures during the last 6 months, according to a family report. Grade 2 or less spastic tone based on the modified Ashworth scale in the flexor muscle group of the wrist and elbow joints. Absence of obvious and noticeable deformity in the upper limbs based on clinical examination. Non-participation in research using "Leap motion" during the last six months. Absence of severe visual impairment.

Exclusion criteria

Exclusion criteria: Reluctance / ability of the child and family to continue participating in the research.

Design outcomes

Primary

MeasureTime frame
Manual skill score in QUEST questionnaire. Timepoint: At the beginning of the study and in the 12th and 16th weeks after the start of the study. Method of measurement: QUEST questionnaire.

Secondary

MeasureTime frame
Power grip. Timepoint: At the beginning of the study and at weeks 12 and 16 after the start of the study. Method of measurement: Dynamometer device.;Lateral pinch, palmar pinch. Timepoint: At the beginning of the study and at weeks 12 and 16 after the start of the study. Method of measurement: pinch gauge device.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsajjad sabbaghi siuki

University of social welfare and rehabilitation sciences

sajadsss1375@gmail.com+98 51 5222 8297

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026