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The Effects of Attentional Focus on Arm Training in Stroke

A Randomized Control Trial on the Effects of Attentional Focus on Motor Training of the Upper Extremity Using Robotics With Individuals After Chronic Stroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02890446
Enrollment
33
Registered
2016-09-07
Start date
2014-05-31
Completion date
2015-11-30
Last updated
2016-09-07

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

Conditions

Stroke

Keywords

attentional focus, upper extremity, hemiparesis, stroke

Brief summary

This study compares the effects of an internal versus an external focus of attention on motor training of the affected arm for individuals with stroke. Participants were randomly assigned to either the internal or external focus treatment groups and received 12 sessions of arm training.

Detailed description

Participants were randomized to one of two treatment groups and received upper arm reaching training on the InMotion 2 shoulder robot (12 hourly sessions over four weeks). The external focus group received instructions specifically to pay attention to the task goal--hitting targets on the video game, while the internal focus group was instructed to pay attention to the movement of their arm motions (video game monitor was turned off). Both groups practiced the same arm reaching pattern and were matched for level of arm impairment and training dosage.

Interventions

BEHAVIORALupper arm training on the InMotion 2 shoulder robot

Both groups practiced shoulder and elbow exercises on a robotic arm device under an external focus or internal focus practice condition. Practiced arm reaching in a clock-like design to facilitate horizontal shoulder flexion, extension, abduction, adduction. 12 sessions--3 times a week for 4 weeks

Sponsors

New York University
CollaboratorOTHER
New York Presbyterian Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnosis of stroke \> 6 months * moderate to severe arm impairment * intact visual scanning and spatial orientation of the affected arm * functional cognitive status * medically stable

Exclusion criteria

* concurrent occupational or physical therapy for the arm * joint contractures at the wrist, forearm, elbow, or shoulder * moderate to severe spasticity at the elbow or shoulder * presence of other neurological conditions * botulinum toxin injection in the affected arm \< 3 months prior * score of 0/5 on manual muscle test at the elbow or shoulder

Design outcomes

Primary

MeasureTime frameDescription
Change in coordination at the shoulder and elbow measured by joint independence after arm training assessed start of training, discharge and at follow up.baseline, 4 weeks, 8 weekskinematic measure of coordination between the shoulder and elbow joint
Change in quality of arm motion measured by smoothness at the start of arm training, at 4week, and 8 weeks.baseline, 4 weeks, 8 weekskinematic assessment of arm motion measured by average velocity decided by maximum velocity
Change in motor impairment of the arm measured by Fugl-Meyer Assessment (FMA) at the start of training, discharge, and follow up.baseline, 4 weeks, 8 weeksperformance based assessment of underlying motor impairment of the affected shoulder, elbow, hand after stroke
Change in motor impairment and functional ability of the arm measured by the Wolf Motor Function Test (WMFT) at start of training, discharge, and follow up.baseline, 4 weeks, 8 weeksperformance based assessment of underlying motor impairment and function of the affected arm after stroke

Outcome results

None listed

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