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Compares treatment options for Stroke
Official title Efficacy of Tele-CPASS Compared to In-person CPASS Therapy for Upper Extremity Motor Recovery
ClinicalTrials.gov ID: NCT07661849
What this study is testing
- What it's testing
- This study evaluates whether a home-based telerehabilitation program (tele-CPASS) is as effective as an in-person rehabilitation program (CPASS) for improving arm and hand function after stroke. Stroke often leads to long-term difficulty using the affected arm in daily activities, and access to in-person therapy can be limited.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 21 and older
You may be able to join if
- Age 21 years or older
- Neuroimaging-confirmed stroke within 40 days prior to enrollment
- Persistent hemiparesis resulting in impaired upper extremity function, defined by a score of 0 to 3 on the NIH Stroke Scale motor arm item
- Able to participate in all study-related activities, including 1-year follow-up
- Short Blessed Memory Orientation and Concentration Scale score less than 8
You likely can't join if
- Inability to provide informed consent
- Persistent disabling neurologic condition, such as multiple sclerosis, Parkinsonism, amyotrophic lateral sclerosis, or dementia requiring medication
- Clinically significant fluctuations in mental status within 72 hours prior to randomization
- Active psychosis, psychosis within the prior 2 years, active substance abuse, or prior substance abuse
- Dense sensory loss, defined by a score of 3 or 4 on the NIH Stroke Scale sensory item
- Ataxia out of proportion to weakness in the affected arm, defined by a score greater than 1 on the NIH Stroke Scale ataxia item
See the full eligibility criteria
- Age 21 years or older
- Neuroimaging-confirmed stroke within 40 days prior to enrollment
- Persistent hemiparesis resulting in impaired upper extremity function, defined by a score of 0 to 3 on the NIH Stroke Scale motor arm item
- Able to participate in all study-related activities, including 1-year follow-up
- Short Blessed Memory Orientation and Concentration Scale score less than 8
- Able to follow 2-step commands
- Montreal Cognitive Assessment (MoCA) score greater than 25
- No upper extremity injury or condition that limited upper extremity use prior to the stroke
- Inability to provide informed consent
- Persistent disabling neurologic condition, such as multiple sclerosis, Parkinsonism, amyotrophic lateral sclerosis, or dementia requiring medication
- Clinically significant fluctuations in mental status within 72 hours prior to randomization
- Active psychosis, psychosis within the prior 2 years, active substance abuse, or prior substance abuse
- Dense sensory loss, defined by a score of 3 or 4 on the NIH Stroke Scale sensory item
- Ataxia out of proportion to weakness in the affected arm, defined by a score greater than 1 on the NIH Stroke Scale ataxia item
- Not expected to survive 12 months because of other illnesses
- Pregnancy
- Severe aphasia
- Receipt of botulinum toxin or expectation of receiving botulinum toxin during the study period
The study team makes the final eligibility decision.
Where it's taking place
- El Paso, Texas, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 21 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include El Paso, Texas, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.