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Stroke, AcuteNCT05417802

Surveying Patient's Interest in Robotic Rehabilitation Device

An observational study of Stroke, Acute, run by State University of New York at Buffalo at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This is a survey study to understand the stroke survivor's interest in robotic training. Investigators will use a questionnaire and show a video of robotic therapy to ask questions on their interest. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Stroke, Acute
How many people
88 participants
Where
1 siteUnited States
Study dates
8 Dec 2021to 23 Apr 2026
Phase
Observational
Are there results?
None posted in the registry

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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Stroke patients

Who may be able to join

  • Adults with stroke
  • Adults with no cognitive difficulties

Who cannot join

  • Adults with pregnancy,
  • Adults with other neurological disorders than stroke
  • Adults with hemorrhagic stroke

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Buffalo General Hospital

    Buffalo, New York, 14203

Other trials in United States

About this study

This is a survey study to understand the stroke survivor's interest in robotic training. Investigators will use a questionnaire and show a video of robotic therapy to ask questions on their interest.

Read the detailed description

The purpose of this research is to investigate the interest of individuals with recent stroke in robotic therapy. Investigators will introduce a novel robotic platform to train ADLs of stroke patients. Investigators will examine the usability of this device as a home trainer for training rotational hand manipulation tasks such as opening a pickle jar, turning a key, missing a pot with a ladle, etc. The device will especially target stroke patients with ischemic stroke to enhance the performance of ADL. Also, investigators will examine the frequency and dosage of the current occupational therapy, followed by the satisfaction of the current therapy. Participant's participation will contribute to the development of a new therapy method using a robotic device for home-based training.

Conditions
Stroke, Acute
Medical subject headings
Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT05417802
Study groupRoleWhat they receive
Stroke with acute strokeInclusion criteria * Episode of single stroke within the past twelve weeks * Individuals' age over 18 years old. Exclusion criteria * Pregnant women , neurological disorders other than stroke (i.e. Parkinson's), non-ischemic stroke * Individuals with severe cognitive impairments (demonstrating difficulty to understand, read, and answer the questions in writing) * Individuals with difficulties to listen the instruction and video of the robotic device

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Current Therapy question - 1

    How many hours are you receiving occupational therapy for each session?

    Measured: through study completion, an average of 1 year

  2. Current Therapy question - 2

    How frequent are you receiving therapy (ex.: 2/week: two times per week)?

    Measured: through study completion, an average of 1 year

  3. Current Therapy question - 3

    When did you start your therapy (how many days after stroke)?

    Measured: through study completion, an average of 1 year

  4. Current Therapy question - 4

    What kind of therapy are you receiving now?

    Measured: through study completion, an average of 1 year

  5. Current Therapy question - 5

    Do you think that the therapy you are receiving is helpful to restore your arm function and help you participate in activities during daily living (example: drinking, feeding, moving objects)?

    Measured: through study completion, an average of 1 year

  6. Current Therapy question - 6

    Do you think that you are receiving enough occupational therapy to help you participate in activities during daily living (example: drinking, feeding, moving objects)?

    Measured: through study completion, an average of 1 year

  7. Interest in Robotic Rehabilitation question - 1

    Do you think that this device can be helpful to improve your arm function from stroke?

    Measured: through study completion, an average of 1 year

  8. Interest in Robotic Rehabilitation question - 2

    Do you think that you will use the device for home training when it is provided?

    Measured: through study completion, an average of 1 year

  9. Interest in Robotic Rehabilitation question - 3

    Do you think that the device is helpful to help you participate in activities during daily living (example: drinking, feeding, moving objects)?

    Measured: through study completion, an average of 1 year

  10. Interest in Robotic Rehabilitation question - 4

    If you have the device at home, how long would you like to exercise with the device?

    Measured: through study completion, an average of 1 year

  11. Interest in Robotic Rehabilitation question - 5

    If you have the device at home, how frequent would like to use this device?

    Measured: through study completion, an average of 1 year

  12. Interest in Robotic Rehabilitation question - 6

    Do you think that the training can be more effective by adding virtual reality?

    Measured: through study completion, an average of 1 year

  13. Interest in Robotic Rehabilitation question - 7

    If the device can apply therapeutic force, which type of force do you prefer for home-training?

    Measured: through study completion, an average of 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Jun 2022
  2. Study start8 Dec 2021
  3. Primary completion23 Apr 2026
  4. Study completion23 Apr 2026

Resources

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
Retrospective
Enrolment
88 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05417802
Sponsor's protocol ID
STUDY00004756
Status last verified
Oct 2026
First submitted
5 Jun 2022
Last updated
28 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The de-identified data will be shared upon request to PI.

Questions about this trial

What is this clinical trial studying?

An observational study of Stroke, Acute, run by State University of New York at Buffalo 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 3 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: finished, as of the sponsor's last update on 28 Oct 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Current Therapy question - 1 (time frame: through study completion, an average of 1 year). The study lists 13 primary outcomes in all. 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 28 Oct 2026.

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