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Quantification of UE Use and Effects of Feedback in the Home Setting

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02995213
Acronym
OPTASpr2016
Enrollment
12
Registered
2016-12-16
Start date
2015-11-30
Completion date
2016-12-31
Last updated
2017-09-26

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

Conditions

Stroke

Brief summary

The investigators are proposing a pilot study, the purpose of which is to use accelerometers to quantify UE use (1 and two hand use) in people post-stroke from which the investigators will develop use-based feedback to improve recovery in the home setting. The objectives of this pilot study are to: 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.

Interventions

BEHAVIORALAccelerometer based feedback about paretic arm use

Sponsors

Cleveland State University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Subjects post-stroke * 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

* can't currently have another neuromuscular disorders such as spinal cord injury, traumatic brain injury, Parkinson disease or multiple sclerosis * no upper extremity injury within the last 3 months

Design outcomes

Primary

MeasureTime frame
Accelerometer based paretic arm amount of use3 week period

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026