C-STAR Movement Database

Center for Smart Use of Technologies to Assess Real World Outcomes Movement Database

The purpose of this study is to develop a database that contains movement and rehabilitation-related data collected through the use of wearable sensors and video. This database will serve as a resource for clinicians and researchers interested in the investigation of movement or rehabilitation-related research ideas.

Study Overview

• Status: Active, not recruiting
• Conditions: Stroke; Parkinson Disease; Lower Limb Amputation Below Knee (Injury); Lower Limb Amputation Above Knee (Injury)
• Intervention / Treatment: Other: Database Entry

Detailed Description

Scholarly research in the field of physical rehabilitation helps to aid in maximizing outcomes for individuals that require these services due to orthopedic and neurologic injuries. To produce quality research results, large cohorts of individuals are often required for data analysis. Some research facilities or labs do not have adequate access to large cohorts or may not have the means to recruit them. By building the C-STAR database, the intent is to create a database that can serve as a hub for data sets that researchers and clinicians with appropriate access may use to support their research questions related to movement and physical rehabilitation.

• Study Type: Observational
• Enrollment (Estimated): 250

Contacts and Locations

Study Locations

• United States
  • Illinois
    • Chicago, Illinois, United States, 60611
      • Shirley Ryan AbilityLab

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: No older than 99 years (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: N/A

• Sampling Method: Non-Probability Sample

Study Population

By building the C-STAR database, the intent is to create a database that can serve as a hub for data sets that researchers and clinicians with appropriate access may use to support their research questions related to movement and physical rehabilitation.

Description

Inclusion Criteria:

1. Age 0 to 99 years old
2. Able and willing to give written consent and comply with study procedures

Exclusion Criteria:

1. Unable to give written consent or comply with study procedures
2. Any condition that would prevent safe completion of study activities, as determined by the Principal Investigator

Study Plan

How is the study designed?

Number of groups / cohorts

4

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Stroke; For this cohort, individuals who have experienced a stroke will be asked to complete a variety of movement related rehabilitation assessments with wearable sensors and audio/video recording.	Other: Database Entry; Database entries will contain wearable sensor, audio, and video data collected during rehabilitation-related movement assessments
Parkinsons Disease; For this cohort, individuals who have been diagnosed with Parkinsons Disease will be asked to complete a variety of movement related rehabilitation assessments with wearable sensors and audio/video recording.	Other: Database Entry; Database entries will contain wearable sensor, audio, and video data collected during rehabilitation-related movement assessments
Lower Limb Amputation; For this cohort, individuals who have experienced a lower limb amputation will be asked to complete a variety of movement related rehabilitation assessments with wearable sensors and audio/video recording.	Other: Database Entry; Database entries will contain wearable sensor, audio, and video data collected during rehabilitation-related movement assessments
Healthy Control; For this cohort, individuals who have no significant neurologic or orthopedic injuries will be asked to complete a variety of movement related rehabilitation assessments with wearable sensors and audio/video recording.	Other: Database Entry; Database entries will contain wearable sensor, audio, and video data collected during rehabilitation-related movement assessments

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Database development	To develop an online database that contains movement and rehabilitation-related data collected with wearable sensors and video that may be accessed, with appropriate permissions, by clinicians and researchers that are interested in the investigation of movement or rehabilitation related research ideas.	Data will be collected and added to the C-STAR database for 3 years

Collaborators and Investigators

• Sponsor: Shirley Ryan AbilityLab
• Investigators: Principal Investigator: Richard Lieber, PhD, Shirley Ryan AbilityLab; Principal Investigator: Arun Jayaraman, PT, PhD, Shirley Ryan AbilityLab; Principal Investigator: Levi Hargrove, PhD, Shirley Ryan AbilityLab

Study record dates

Study Major Dates

• Study Start (Actual): August 19, 2022
• Primary Completion (Estimated): December 31, 2026
• Study Completion (Estimated): December 31, 2026

Study Registration Dates

• First Submitted: July 20, 2022
• First Submitted That Met QC Criteria: July 20, 2022
• First Posted (Actual): July 22, 2022

Study Record Updates

• Last Update Posted (Actual): May 12, 2026
• Last Update Submitted That Met QC Criteria: May 7, 2026
• Last Verified: May 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Synucleinopathies; Cerebrovascular Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases; Neurodegenerative Diseases; Movement Disorders; Parkinsonian Disorders; Basal Ganglia Diseases; Stroke; Wounds and Injuries; Parkinson Disease
• Other Study ID Numbers: STU00216350

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No