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Developing technology-based hand and arm activity tracking for children with hemiplegia

Developing technology-based hand and arm activity tracking for children with hemiplegia: the TwoCan Project

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN24515760
Enrollment
100
Registered
2019-11-18
Start date
2020-01-01
Completion date
Unknown
Last updated
2023-03-20

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

Conditions

Hemiplegic cerebral palsy (HCP) Nervous System Diseases Cerebral palsy

Interventions

Following baseline observational assessments of hand function, participants will wear two wrist-worn devices, on one each wrist which will measure the participants’ arm movements. They will wear the d

Sponsors

The Newcastle Upon Tyne Hospitals NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Children/young people (male or female) with HCP who: are 8-18 years old, and have Manual Ability Classification (MACS) level I-III 2. Typically developing controls (male or female) who: are 8-18 years old, and have normal hand function 3. Therapists of children with HCP who: are either physiotherapists or occupational therapists, and provide input related to upper limb function 4. For all of the above, adequate command of the English language and fully informed consent are required

Exclusion criteria

Exclusion criteria: 1. Those registered blind or partially sighted 2. Those unable to detect vibratory cues to wrist from the device 3. Those with significant cognitive and/or language deficit precluding ability to use the device and application 4. Those with current involvement in another research study likely to interfere with the conduct of this study

Design outcomes

Primary

MeasureTime frame
1. Feasibility and acceptability of the approach assessed through qualitative interviews with participants at the end of the study 2. Recruitment rate recorded as the number of eligible participants who consent to participate in the study within 6 months 3. Attrition rate recorded as the number of participants who consent to participate that remain in the study until the end of follow up at 10 weeks

Secondary

MeasureTime frame
Arm movement measured by wrist-worn accelerometer continuously for approximately 12 hours/day for the whole 10-week period

Countries

England, United Kingdom

Outcome results

None listed

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