NCT06653855 · Scott Getsoian
The Effect of Cupping on Spasticity and Function of the Lower Extremity During Rehabilitation After Stroke
What this study is about
Physical therapists use dry static cupping for the treatment of many conditions, including spasticity for patients post-stroke. While research better describes the effects of dry static cupping for patients with orthopedic conditions, information is lacking on central conditions, such as stroke and resulting spasticity.
View original scientific description
Physical therapists use dry static cupping for the treatment of many conditions, including spasticity for patients post-stroke. While research better describes the effects of dry static cupping for patients with orthopedic conditions, information is lacking on central conditions, such as stroke and resulting spasticity.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Acute stroke (within 6 months of stroke), with spasticity \& hemiparesis of LE
- Referred by doctor for rehabilitation for a stroke-related condition
- Attending Ascension Rehabilitation of Joliet for rehabilitation
- Able to read or verbally understand English or Spanish
Exclusion criteria
- Absent sensation of the areas to be cupped
- Significant cognitive impairment
- Prescription anticoagulant medications
- Blood clotting disorder
- Uncontrolled hypertension
- Uncontrolled diabetes
- Open wounds within the cupping area
- Current DVT
- Hematoma over the cupping area
- Fracture over the cupping area
- Active cancer within the cupping area
- Current use of Baclofen
- Current use of Botox
- Current use of an anti-spasticity medication
Where
- Joliet, Illinois
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Dec 13, 2024 · Source of record for eligibility and locations