NCT07042152Recruiting
Wearable Device and Behavioral Support for Enhancing Arm Use After Stroke
Sensor Enhanced Activity Motivation After Stroke
Source: ClinicalTrials.gov · Last updated 19 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The goal of this study is to determine the effectiveness of behavioral support and feedback from a wearable device that senses arm movement in improving upper extremity function in a pilot, randomized controlled trial with chronic stroke patients
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 32 (estimated)
- First submitted
- 19 May 2025
- Start date
- 20 Aug 2025
- Primary completion date
- 31 Dec 2025
- Lead sponsor
- University of California, Irvine
- Diseases
- Stroke
- NCT number
- NCT07042152
What you commit to
- Study type: Interventional
- Planned participants: 32
- From 20 Aug 2025 to the primary completion date, 31 Dec 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Plans to alter any current participation in other rehabilitation therapy in the time period of the study
- A history of significant alcohol or drug abuse in the prior 3 years
Other illness
- Single or multiple, ischemic or hemorrhagic stroke less than 6 months ago
- Advanced liver, kidney, cardiac, or pulmonary disease
- Coexistent major neurological disease
- Coexistent major psychiatric disease
- Current enrollment in another study related to stroke or stroke recovery
Other
- Any substantial decrease in alertness, language reception, or attention
- Severe muscle tone at the upper extremity (score ≥ 3 on the Modified Ashworth Spasticity scale)
- Pregnant or lactating
- A terminal medical diagnosis consistent with survival \< 1 year
- Any other medical contraindication to participation in the study, as evaluated by our team physician.
- Visual Analog of Pain Scale Score of 7 or greater
Who the study is looking for
- 18 to 85 years of age
- Experienced a single or multiple, ischemic or hemorrhagic stroke, with unilateral weakness, over six months previously
- An ability to score at least 3 blocks on the Box and Block Test. BBT score of the affected arm is at least 5% worse than that present with the unaffected arm.
- Absence of major depression, as defined by DSM V criteria or a score on the Geriatric Depression Scale \< 10.
Age in the registry: 18 years to 84 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of California, Irvine Coordinator of this site? Confirm its status | Irvine | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.