BridgeMD
New treatment option for Stroke
Official title Emotional Recovery Post-Stroke
ClinicalTrials.gov ID: NCT06782321
What this study is testing
- What it's testing
- The purpose of this study is to evaluate whether adding an emotional wellness component to occupational therapy (OT) and/or speech therapy (ST) telerehabilitation improves overall emotional well-being and activity participation for people with stroke.
- Time commitment: about 8 weeks
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
- Self-reported stroke-related deficits in emotional wellness such as anxiety, sleep disturbance, dread, fear, loss of hope, sadness.
- Have experienced ischemic or hemorrhagic stroke at least 30 days prior
- Stroke-related aphasia and/or upper extremity hemiparesis
- Aged 21 years or older
- English as primary language
You likely can't join if
- Unable to follow 1-2 step instructions given by the study team member during the informed consent procedures.
- Pain that interferes with ability to participate in the study's upper extremity movement tasks.
- Have impaired decision making capacity as determined by the U-ARE protocol for assessing capacity to provide informed consent.
See the full eligibility criteria
- Self-reported stroke-related deficits in emotional wellness such as anxiety, sleep disturbance, dread, fear, loss of hope, sadness.
- Have experienced ischemic or hemorrhagic stroke at least 30 days prior
- Stroke-related aphasia and/or upper extremity hemiparesis
- Aged 21 years or older
- English as primary language
- Have corrected vision to be able to read text on a screen
- Able to participate fully in the study's tele-rehabilitation (Aim 1) and/or virtual group programing (Aim 2) with personally owned device (i.e., phone, tablet, or laptop) and personal Wi-Fi connection or cellular service
- Cognitive, language, and motor capacity to participate fully in the study's assessment session as per the judgment of the licensed, experienced stroke tele-rehabilitation occupational or speech therapist
- Unable to follow 1-2 step instructions given by the study team member during the informed consent procedures.
- Pain that interferes with ability to participate in the study's upper extremity movement tasks.
- Have impaired decision making capacity as determined by the U-ARE protocol for assessing capacity to provide informed consent.
The study team makes the final eligibility decision.
Where it's taking place
- Charleston, South Carolina, 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 study runs about 8 weeks per participant, based on its public description. The team confirms the exact schedule and number of visits before you 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 Charleston, South Carolina, 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.