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Official title Effects Of Neurocognitive Therapy With And Without Soft Robotic Hand On Hand Function
ClinicalTrials.gov ID: NCT06927284
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 40 to 60
You may be able to join if
- 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
You likely can't join if
- Participants who have a history of significant neurological or orthopedic disorders, other than stroke, that could interfere with upper limb motor or...
- 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) .
- Participants who have active pacemakers and other active implants.
See the full eligibility criteria
- 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)
- 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) .
- Participants who have active pacemakers and other active implants.
The study team makes the final eligibility decision.
Where it's taking place
- Lahore, Punjab Province, Pakistan
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 40 years to 60 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Lahore, Punjab Province, Pakistan. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.