No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
21 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
80 (estimated)
Sponsor
Medical University of South Carolina · Other
Who this trial is looking for
This trial is looking for people who have had a stroke and are dealing with emotional challenges like anxiety or sadness. Participants will receive emotional wellness support along with occupational or speech therapy through tele-rehabilitation.
Are You a Good Fit for This Trial?
You may be able to join if
I have emotional wellness issues after my stroke.
I had a stroke at least 30 days ago.
I have difficulty speaking or weakness in my arm from the stroke.
I am at least 21 years old.
I speak English as my primary language.
I can see clearly enough to read text on a screen.
I have my own device and internet to join the virtual programs.
I can participate fully based on my therapist's judgment.
You may not be able to join if
I cannot follow simple instructions during the consent process.
I have pain that makes it hard to do movement tasks.
I have trouble making decisions about my care.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion 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 ye…
Inclusion 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
Exclusion Criteria:
* 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.
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