Ignite Creation Date:
2024-07-17 @ 11:37 AM
Last Modification Date:
2024-10-26 @ 3:34 PM
Study NCT ID:
NCT06498011
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-07-12
First Post:
2024-06-24
Brief Title:
COgnitive-somatoSensory-MOtor Training to Improve Arm and Hand Function After Stroke iCOSMO
Sponsor:
University Health Network Toronto
Organization:
University Health Network Toronto
Study Overview
Official Title:
Comparing the Effect of a Graded Repetitive Arm Supplementary Home-based Exercise Programme With COgnitive-somatoSensory-MOtor Training to Improve Arm and Hand Function After Stroke iCOSMO
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
iCOSMO
Brief Summary:
The iCOSMO study investigates the feasibility and beneficial effects of an intervention combining sensation motor and cognition to improve arm and hand function after chronic stroke
Detailed Description:
The iCOSMO is a two-arm randomized controlled trial study evaluating the feasibility and efficacy of combined somatosensory-motor intervention using a cognitive approach to improve upper limb recovery in people with chronic stroke Forty participants will be recruited 20 in experimental group and 20 in the control group iCOSMO will include active touch and movement exploratory procedures during goal-oriented tasks as well as robotic training using the Kinarm Exoskeleton device The experimental group will receive a total of 36 hours of treatment 6 weeks The control group will receive a matched dose of a home-based motor exercise programme The outcome measures will include measures of feasibility such as the recruitment and adherence rates and standardised clinical and robotic assessments The participants will be tested at the start and end of the baseline phase at post-intervention and at 1-month follow-up
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None