Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
NCT06782321

Emotional Recovery Post-Stroke

Led by Medical University of South Carolina · Updated on 2025-05-23

80

Participants Needed

1

Research Sites

134 weeks

Total Duration

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Sponsors

M

Medical University of South Carolina

Lead Sponsor

T

The Duke Endowment

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Emotional Recovery Post-Stroke

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Self-reported stroke-related deficits in emotional wellness such as anxiety, sleep disturbance, dread, fear, loss of hope, sadness.
  • 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
  • Corrected vision adequate to read text on a screen
  • Able to fully participate in telerehabilitation and/or virtual group programming using a personal device and personal internet or cellular service
  • Cognitive, language, and motor ability to fully participate in assessment sessions as judged by a licensed stroke telerehabilitation therapist
Not Eligible

You will not qualify if you...

  • Unable to follow 1-2 step instructions during informed consent procedures
  • Pain that interferes with ability to perform upper extremity movement tasks
  • Impaired decision-making capacity as determined by the U-ARE protocol for consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical University of South Carolina

Charleston, South Carolina, United States, 29425

Actively Recruiting

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Research Team

K

Kelly Rishe

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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