NCT05659875Completed
CompARing Long terM Outcomes in Chronic Stroke Survivors Across Investigational Assessments Following a Prescribed Upper Extremity Exercise Program
CompARing Long terM Outcomes in Chronic Stroke Survivors Across Investigational Assessments Following a Prescribed Upper Extremity Exercise Program (ARM-PROGRAM)
Source: ClinicalTrials.gov · Last updated 9 Dec 2024
Brief summary (registry, in English)
The purpose of the study is to compare assessments of arm function following a standard exercise program in chronic stroke patients.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 1 (actual)
- First submitted
- 12 Dec 2022
- Start date
- 21 Feb 2023
- Primary completion date
- 21 Mar 2024
- Lead sponsor
- The University of Texas Health Science Center, Houston
- Diseases
- Stroke
- NCT number
- NCT05659875
What you commit to
- Study type: Interventional
- Participants enrolled: 1
- From 21 Feb 2023 to the primary completion date, 21 Mar 2024
- 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
- Prior arm injury impacting available passive or active range of motion or significant arm pain with movement
- Prior significant drug or alcohol abuse
- History of clinically significant ischemic or hemorrhagic stroke prior to index stroke resulting in prior arm injury or weakness.
Other illness
- Underlying brain pathologies such as metastatic or primary brain malignancies, comorbid multiple sclerosis, etc.
- Diagnosed with dementia
- Pre-stroke baseline modified Rankin Scale (mRS) \>3
- History of seizure/epilepsy
- Medical instability assessed by the treating stroke physician to participate to the study.
Other
- Pregnancy
- Contraindication to MRI or Transcranial Magnetic Stimulation (TMS).
Who the study is looking for
- Single qualifying stroke event as confirmed by CT or MRI
- At least 1 month post stroke
- Score of at least 2-/5 on Manual Muscle Test for wrist flexors or extensors, indicating adequate movement to complete robotic device use
- Able to follow written instructions
Age in the registry: 18 years to 80 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 |
|---|---|---|---|
| The University of Texas Health Science Center at Houston Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.