Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:47 PM
Ignite Modification Date:
2025-12-24 @ 9:47 PM
NCT ID:
NCT05878132
Eligibility Criteria:
Inclusion Criteria:
* age ≥ 18 years
* unilateral hemispherical involvement
* diagnosis of stroke with onset ≥ three months
* hemiplegic upper limb with Functional test for hemiplegic upper extremity-Hong Kong version (FTHUE-HK) ≥ score of 3 (maximum of 7) (Fong et al., 2004).
* no complaint of excessive pain and swelling over the hemiplegic arm
* able to provide informed consent to participate.
Exclusion Criteria:
* participating in another similar form of experimental study during the same period
* having a history of botulinum toxin injection in the past three months
* having other significant upper limb impairment, i.e. fixed contractures, frozen shoulder, and severe arthritis
* having a diagnosis which would interfere in the use of the device, i.e. visual impairment, active cardiac issues and palliative treatment.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05878132
Study Brief:
Protocol Section:
NCT05878132