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Functional Connectivity In Relation To Proprioception and Sensorimotor Recovery in Stroke Patients (Feasibility Study)

Functional Connectivity In Relation To Proprioception and Sensorimotor Recovery in Stroke Patients (Feasibility Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02445768
Enrollment
43
Registered
2015-05-15
Start date
2015-12-31
Completion date
2023-02-28
Last updated
2023-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Brief 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.

Interventions

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Preliminary study to measure the brain mechanisms of cognitive multisensory rehabilitation8 weeksThe 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026