Neurocognitive therapy with or without a soft robotic hand for hand recovery after stroke
Compares neurocognitive therapy, with and without a robotic glove, in people recovering from stroke.
Plain-language title generated from the registry record
Registry title: Effects Of Neurocognitive Therapy With And Without Soft Robotic Hand On Hand Function
Key facts
- Where
- Lahore, PakistanSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 40 and 60 years old?
Source: NCT06927284, who can take part
Where in Pakistan
- Sheikh Zayad HospitalLahore, PakistanTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Riphah International University
- Trial code
- NCT06927284
- Record updated
- 22 August 2025
- Original description
To determine the effect of neurocognitive therapy with and without a soft robotic hand on manual ability, dexterity, strength, spasticity and upper limb function in sub-acute stroke.Read full original descriptionShow less
Effects of Neurocognitive Therapy With and Without Soft Robotic Hand on Hand Function in Sub-acute Stroke
To determine the effect of neurocognitive therapy with and without a soft robotic hand on manual ability, dexterity, strength, spasticity and upper limb function in sub-acute stroke.
Inclusion: Participants of Post stroke patients (6-12 weeks ); Participants with Spasticity < 2 on modified Ashworth scale; Participants with first ever stroke; Participants with normal cognition > 24 on MoCA; Participants must be able to provide informed consent; Hemiparesis with arm motor deficit as assessed by with NIHSS >1(14).
Exclusion: Participants who have active pacemakers and other active implants; Participants who have a history of significant neurological or orthopedic disorders, other than stroke, that could interfere with upper limb motor or sensory recovery; Participants who have altered state of consciousness, severe aphasia, severe cognitive deficit; Participants who have severe pathologies of traumatic and or rheumatic nature, severe pain in effected arm (>5 on visual analog scale for pain) .