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Stroke Inpatient Rehabilitation Reinforcement of ACTivity

Stroke Inpatient Rehabilitation Reinforcement of ACTivty: An International Multisite Clinical Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01246882
Acronym
SIRRACT
Enrollment
140
Registered
2010-11-23
Start date
2011-01-31
Completion date
2012-11-30
Last updated
2019-05-01

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

Conditions

Stroke

Keywords

Stroke, gait, walking, disability, wireless inertial sensing, mobile health

Brief summary

The purpose of this study is to determine the effects of daily feedback about physical activity (number of bouts of walking, duration of bouts, total walking distance, average and fastest walking speed) and walking average speed compared to feedback about walking speed only on walking-related outcomes during inpatient rehabilitation for stroke. For the first time, daily walking and other exercise will be monitored by bilateral triaxial accelerometers on the ankles. Activity-recognition algorithms will analyze the inpatient sensor data and return a summary to the participants at each site.

Detailed description

Wireless Sensor System The inertial sensor system and activity-recognition algorithms were previously described and tested for short-term reliability. Three sets of triaxial accelerometers (Gulf Coast Data Concepts, Waveland, MS) were mailed to each site's coordinator. Therapists placed one sensor on each ankle before participants got out of bed each morning and removed them once they were in bed at the end of the day; sensor use during weekends was optional. A soft snap band secured each sensor proximal to the medial malleolus, flush against the bony tibia. Every night, sensors were plugged into a local computer to recharge while accelerometer data were uploaded to the central server at UCLA for secure storage and processing. Sensor Calibration and Data Processing In recognition of the variations in gait speed and stand and swing symmetry that occur in patients who need inpatient rehabilitation after stroke, we chose to generate individual templates of each participant's gait from a pair of standardized walks. On study entry participants performed two stopwatch- timed 10-meter walks at self-selected casual and safest fast walking speeds. A hybrid classifier employing dynamic time warping and Naïve Bayes algorithms generated statistical models of each participant's gait based on the two walks. Repeat walks were performed and the templates updated weekly for the remainder of each participant's rehabilitation stay to account for expected changes in gait parameters.

Interventions

BEHAVIORALAugmented activity feedback

Feedback about walking speed and amount of physical activity will be provided 3 times per week from data acquired from wireless sensors on each ankle.

BEHAVIORALSpeed-only feedback

Feedback about walking speed will be provided 3 times per week.

Sponsors

National Taiwan University Hospital
CollaboratorOTHER
Washington University School of Medicine
CollaboratorOTHER
University of Vigo
CollaboratorOTHER
Morinomiya Hospital, Osaka, Japan
CollaboratorUNKNOWN
Mayo Clinic
CollaboratorOTHER
IRCCS San Camillo, Venezia, Italy
CollaboratorOTHER
Fairlawn Hospital, Worcester, MA, USA
CollaboratorUNKNOWN
Chonnam National University Hospital
CollaboratorOTHER
Ain Shams University
CollaboratorOTHER
MedStar National Rehabilitation Network
CollaboratorOTHER
St. Luke's Hospital, Pennsylvania
CollaboratorOTHER
Father Muller Medical College
CollaboratorOTHER
Burke Rehabilitation Hospital
CollaboratorOTHER
Burwood Hospital, Christchurch, New Zealand
CollaboratorOTHER
Gazi University
CollaboratorOTHER
University College Hospital, Ibadan, Nigeria
CollaboratorUNKNOWN
Rehabilitation Hospital, Barcelona, Spain
CollaboratorUNKNOWN
IRCCS San Raffaele
CollaboratorOTHER
University of California, Los Angeles
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

* Admission for acute inpatient rehabilitation of a first stroke (or second stroke after full recovery from prior TIA/Stroke) * Time from onset of stroke to admission for rehabilitation \< 35 days * Stroke from any cause (thrombotic infarct, cardioembolus, intracerebral hemorrhage) that includes unilateral hemiparesis. Hemiparesis means less than / equal to 4/5 strength by the British Medical Council scale for hip flexion tested supine and for knee or ankle flexion and extension (scores less than / equal to 22 of 25 possible points) * Ability to follow simple instructions, especially to understand verbal reinforcement about activity. * Independent in mobility prior to admission by the Barthel Index. * Able to walk with no more than physical assistance of 2 persons for at least 5 steps (for example, 3 strides of the left leg alternating with 2 on the right leg). Subjects can use any type of assistive device and brace needed. * Able to understand and repeat information related to the Informed Consent. The subject signs a Consent form.

Exclusion criteria

* Current medical disease that will limit physical therapy at the time of randomization or limited walking prior to the stroke, such as serious infection, DVT, orthostatic hypotension, \> stage 2 decubitus ulcer of buttocks or legs, congestive heart failure, claudication, and pain with weight-bearing or walking. Subjects can be entered if a complication resolves within 7 days of admission screening. * Aphasia with inability to follow 2-step directions during therapeutic instructions or answers Yes/No to questions with \< 75% accuracy related to personal health and symptoms.

Design outcomes

Primary

MeasureTime frame
Gait speedDischarge

Secondary

MeasureTime frame
Distance walked in 3 minutesDischarge

Countries

Egypt, India, Ireland, Italy, Japan, New Zealand, Nigeria, South Korea, Spain, Taiwan, Turkey (Türkiye), United States

Outcome results

None listed

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