Implementing Technology Enhanced Real Time Action Observation Therapy in Persons With Chronic Stroke (TERTAOT)

University of Michigan

Status: Completed

Conditions: Hemiparesis; Hemiplegia; Chronic Stroke; Paralysis

Treatments: Device: Real-time action observation with augmented Kinect

Study type: Interventional

Funder types: Other

Identifiers

NCT03780296

HUM00121813

Details and patient eligibility

About

This is a feasibility study to alter the Microsoft Kinect software to be used as a rehabilitation tool. The prototype used is still in the early developing stage. The purpose of this research study is to develop a prototype of altered Microsoft Kinect Software and determine its use in improving the function of the study subjects' weaker extremities. The altered software will allow a viewing of the mirror image of the involved limb as it is moved. However, the image that is viewed will reflect normal movement even if the limb cannot move normally. By viewing normal movement of the weaker limbs the "mirror neuron" network in the brain will become activated and will ultimately improve the function of the weaker side.

Enrollment: 18 patients

Sex: All

Ages: 40 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• • Adults 40 years of age and older having had a stroke greater than 6-months post onset
• Able to follow commands in English
• Medically stable and without acute illness, such as infection, inflammation, ongoing chest pain, or short of breath with walking and light activities
• Able to stand up off of a standard height chair (16-18 inches)

Exclusion criteria

• • Cognitive impairment as measured by a score below 24/30 on Mini Mental State Examination
• A diagnoses of cancer involving the nervous or musculoskeletal system
• Severe pain in arms, legs, or spine measured by >6/10 using Verbal Numerical Pain Rating Scale that prevents them from standing or walking independently
• Diagnoses of other neurological diseases except for stroke, such as spinal cord injury or Parkinson's disease etc.
• Individuals at the advanced stage of a disease and with less than 12 months to live.

Trial design

Primary purpose: Device Feasibility

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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18 participants in 1 patient group

Real-Time Action Observation with augmented Kinect

Experimental group

Description:

Participants will receive 30 minutes of the augmented kinect software in real-time undergoing an exercise protocol involving seated upper extremity exercises, seated lower extremity exercises and standing upper extremity exercises.

Treatment:

Device: Real-time action observation with augmented Kinect