Skip to content

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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03780296
Acronym
TERTAOT
Enrollment
18
Registered
2018-12-19
Start date
2017-09-05
Completion date
2018-09-26
Last updated
2018-12-19

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

Conditions

Chronic Stroke, Hemiparesis, Hemiplegia, Paralysis

Keywords

Kinect, Rehabilitation, Virtual reality, Mirror therapy

Brief summary

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.

Interventions

DEVICEReal-time action observation with augmented Kinect

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.

Sponsors

University of Michigan-Flint
CollaboratorUNKNOWN
University of Michigan
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE

Intervention model description

Single group pre-test/post-test design

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Motor Activity Log (MAL)5 monthsMAL measures participants overall use or increased use and quality of use of affected upper limb
Change in 9 Hole Peg Test (9HPT)5 months9 HPT is a timed standardized measure participants overall function of dexterity.
Change in 10 Meter Walk Test (10mWT)5 monthsThe 10mWT is a standardized measure used to assess participants timed walking speed in meters per second over a short distance
Change in Functional Reach Test (FRT)5 monthsThe functional reach test is a standardized measure assessing the participants ability to reach forward with unaffected arm
Change in Timed Up and Go (TUG)5 monthsThe TUG is a standardized measure which assesses participants mobility, balance, walking ability, and fall risk in older adults
Change in 5 Time Sit to Stand (5xSS)5 monthsThis is a standardized measure assessing participants functional lower limb strength.

Countries

United States

Outcome results

None listed

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