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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02445768
Other study ID # PMR-2015-23168
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 2015
Est. completion date February 28, 2023

Study information

Verified date March 2023
Source University of Minnesota
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose now is to: 1. identify brain connections related to proprioception to have a better understanding of differences between people with stroke and healthy persons 2. evaluate how these brain connections will change in people with stroke when they are engaged in 6-week cognitive multisensory rehabilitation.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date February 28, 2023
Est. primary completion date February 28, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: Inclusion criteria for healthy subjects are: - medically stable; - 18 - 99 years of age; - able to hear the instructions given during the study Inclusion criteria for stroke patients are: - at least 6 months post-stroke; - medically stable; - 18 - 99 years of age; - subcortical or cortical infarct confirmed with MRI; - Mini-mental State Exam > 24/30 (Folstein et al., 1975); - able to hear the instructions given during the study; - able to comprehend the instructions given during the study; - able to commit time to participate in a 6-12-weeks rehabilitation program Exclusion Criteria: - having ever experienced a stroke or another brain injury or illness related to the brain that has lasting effects or effects experienced at the moment of recruitment; - severe sensory impairments such that different movements of the finger, hand or wrist are not reliably felt; - contractures in tested arm that hinder persons from keeping the outstretched arm in a relaxed position; - interfering comorbidities (e.g. fracture, cancer, peripheral neuropathy); - exhibit contra-indications to enter the magnetic field of the 3T (pacemakers, metal parts in the body etc); - pregnant or nursing mother; - adults lacking capacity to consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cognitive multisensory rehabilitation


Locations

Country Name City State
United States University of Minnesota Medical Center Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota

Country where clinical trial is conducted

United States, 

References & Publications (1)

Van de Winckel A, De Patre D, Rigoni M, Fiecas M, Hendrickson TJ, Larson M, Jagadeesan BD, Mueller BA, Elvendahl W, Streib C, Ikramuddin F, Lim KO. Exploratory study of how Cognitive Multisensory Rehabilitation restores parietal operculum connectivity and improves upper limb movements in chronic stroke. Sci Rep. 2020 Nov 20;10(1):20278. doi: 10.1038/s41598-020-77272-y. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Preliminary study to measure the brain mechanisms of cognitive multisensory rehabilitation The robots will be used for research in healthy adults and stroke patients in the proposed studies below and are designed to mimick the exercises given during cognitive multisensory rehabilitation. The robots have been tested and cleared by the 3T safety committee at the CMRR, U of M. The first objective is a feasibility study to investigate the brain mechanisms of cognitive multisensory rehabilitation, through use of the robot in the 3T scanner at the U of M in healthy participants with stroke. Changes in brain function will be measured in individuals with stroke who will receive 8 weeks of therapy. 8 weeks
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