Quantification of UE Use and Effects of Feedback in the Home Setting
NCT ID: NCT02995213
Last Updated: 2017-09-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
12 participants
INTERVENTIONAL
2015-11-30
2016-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
i.) determine the feasibility of using accelerometers to quantify amount of UE use in the home setting in individuals chronic post-stroke,
ii.) quantify and compare the unilateral activity of the weaker (paretic) versus stronger (non-paretic) UEs, and
iii.) assess the effect of a 7 sessions of in-home accelerometer used-based feedback on unilateral and bilateral UE use.
iv.) assess kinematic, kinetic, and EMG data during UE movements unilaterally and bilaterally in subjects post-chronic stroke pre and post feedback.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Feedback Intervention
Accelerometer based feedback about paretic arm use
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Accelerometer based feedback about paretic arm use
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* chronic post ischemic or hemorrhagic cortical or subcortical stroke
* 25 - 100 years old
* upper extremity impairment
* Subjects will need to be able to flex their paretic shoulder and their elbow \> 40° without assist
* able to follow 2-step commands
* community dwelling with or without assistance
* intact superficial light touch sensation in both upper extremities
* must also have some movement in both arms
Exclusion Criteria
* no upper extremity injury within the last 3 months
25 Years
100 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cleveland State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Maureen Whitford
Assistant Professor
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
IRB-FY2016-84
Identifier Type: -
Identifier Source: org_study_id