StrokeNCT05471375
C-STAR Movement Database
An observational study of Stroke and Parkinson Disease, run by Shirley Ryan AbilityLab at 1 site in United States.
Trial summary
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. Read more about this study
- Who is it for?
- Ages Up to 99 years
- Conditions the study is for
- Stroke, Parkinson Disease, Lower Limb Amputation Above Knee (Injury)
- What is being tested?
- Database Entry
- How many people
- 250 participants
- Where
- 1 siteUnited States
- Study dates
- 19 Aug 2022to 31 Dec 2026
- How long will I take part?
- 7 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Up to 99 years
- All sexes
- Child, Adult, Older adult
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.
Who may be able to join
- Age 0 to 99 years old
- Able and willing to give written consent and comply with study procedures
Who cannot join
- Unable to give written consent or comply with study procedures
- Any condition that would prevent safe completion of study activities, as determined by the Principal Investigator
Trial locations and contacts
1 site in 1 country.
About this study
Official title: 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.
Read the 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.
- Conditions
- Stroke, Parkinson Disease, Lower Limb Amputation Above Knee (Injury), Lower Limb Amputation Below Knee (Injury)
- Being tested
- Database Entry
- Medical subject headings
- Stroke, Parkinson Disease, Wounds and Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Database EntryOther
Database entries will contain wearable sensor, audio, and video data collected during rehabilitation-related movement assessments
| Study group | Role | What they receive |
|---|---|---|
| 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. Receives: Other: Database Entry | |
| 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. Receives: Other: Database Entry | |
| 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. Receives: Other: Database Entry | |
| 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. Receives: Other: Database Entry |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: Data will be collected and added to the C-STAR database for 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jul 2022
- Study start19 Aug 2022
- Primary completion31 Dec 2026 (estimated)
- Study completion31 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for StrokeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 250 participants (estimated)
- Target duration
- 7 Years
Sponsor and investigators
- Lead sponsor
- Shirley Ryan AbilityLab
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Arun Jayaraman, PT, PhD, Shirley Ryan AbilityLab
- Investigators
- Arun Jayaraman, PT, PhD, Principal investigator, Shirley Ryan AbilityLabLevi Hargrove, PhD, Principal investigator, Shirley Ryan AbilityLabRichard Lieber, PhD, Principal investigator, Shirley Ryan AbilityLab
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05471375
- Sponsor's protocol ID
- STU00216350
- Status last verified
- May 2026
- First submitted
- 20 Jul 2022
- Last updated
- 12 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 12 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Center for Smart Use of Technologies to Assess Real World Outcomes Movement Database
- ClinicalTrials.gov ID
- NCT05471375
- Acronym / sponsor ID
- STU00216350
- Conditions
- Stroke, Parkinson Disease, Lower Limb Amputation Above Knee (Injury), Lower Limb Amputation Below Knee (Injury)
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 250 participants (estimated)
- Lead sponsor
- Shirley Ryan AbilityLabUniversity, hospital or other
- Study start
- 19 Aug 2022 (actual)
- Primary completion
- 31 Dec 2026 (estimated)
- Study completion
- 31 Dec 2026 (estimated)
- First posted
- 22 Jul 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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 design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Target follow-up
- 7 Years
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Stroke | – | Other: Database EntryFor 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. |
| Parkinsons Disease | – | Other: Database EntryFor 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. |
| Lower Limb Amputation | – | Other: Database EntryFor 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. |
| Healthy Control | – | Other: Database EntryFor 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. |
Who may qualify
- Ages
- Up to 99 years
- Sex
- All
- Age groups
- Child, Adult, Older adult
- 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.
Key inclusion criteria (2 listed)
- Age 0 to 99 years old
- Able and willing to give written consent and comply with study procedures
Key exclusion criteria (2 listed)
- Unable to give written consent or comply with study procedures
- Any condition that would prevent safe completion of study activities, as determined by the Principal Investigator
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Database EntryDatabase entries will contain wearable sensor, audio, and video data collected during rehabilitation-related movement assessments | Other | Healthy Control, Lower Limb Amputation, Parkinsons Disease, Stroke |
Primary outcome
Database development
Time frame: Data will be collected and added to the C-STAR database for 3 years
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.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 May 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Arun Jayaraman, PT, PhD principal investigator
Shirley Ryan AbilityLab
Levi Hargrove, PhD principal investigator
Shirley Ryan AbilityLab
Richard Lieber, PhD principal investigator
Shirley Ryan AbilityLab
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Stroke and Parkinson Disease, run by Shirley Ryan AbilityLab at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 12 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Database development (time frame: Data will be collected and added to the C-STAR database for 3 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2026.