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Recruiting NCT06596187

NCT06596187 Differential Assessment of Hypertonia

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Clinical Trial Summary
NCT ID NCT06596187
Status Recruiting
Phase
Sponsor Chang Gung University
Condition SCI - Spinal Cord Injury
Study Type INTERVENTIONAL
Enrollment 45 participants
Start Date 2024-10-09
Primary Completion 2026-08

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Continuous passive motion device (CPM) of ankle - fastContinuous passive motion device (CPM) of ankle - slow

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 45 participants in total. It began in 2024-10-09 with a primary completion date of 2026-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Spasticity and rigidity are common symptoms of central nervous system injuries, such as spinal cord injury and Parkinson's disease, and result in distinct patterns of increased resistance during passive joint movements. Spasticity is characterized by a velocity-dependent increase in stretch reflexes, accompanied by exaggerated tendon responses, while rigidity is marked by consistent resistance throughout the range of motion, traditionally considered independent of stretch velocity. However, recent studies suggest that rigidity may also be influenced by stretch velocity. This study aims to investigate muscle tone by examining spasticity, rigidity, and normal muscle function through neural and biomechanical changes. Standard clinical tools, such as the Modified Ashworth Scale and Unified Parkinson's Disease Rating Scale, along with additional assessments like the Myoton and Post-Activation Depression (PAD), will be employed.

Eligibility Criteria

Health subjects: Exclusion Criteria: 1. Musculoskeletal injuries on legs. 2. Osteoporosis. SCI subjects: Inclusion Criteria 1. Participants with chronic spinal cord injury, with injury duration greater than one year. Exclusion Criteria 1. Current musculoskeletal or joint injuries in the lower limbs. 2. History of central or peripheral neuromuscular diseases. 3. Presence of a pacemaker. 4. Current use of antispastic or antidepressant medications. 5. Current venous thromboembolism or osteoporosis. 6. Impairment of the soleus H-reflex arc. PD subjects: Inclusion Criteria: \- Clinical diagnosis of Parkinson disease. Exclusion Criteria: 1. Musculoskeletal injuries on legs 2. Osteoporosis. 3. Any peripheral or central nervous system injury or disease patients.

Contact & Investigator

Central Contact

Ya-Ju Chang, PhD

✉ yjchang@mail.cgu.edu.tw

📞 +88632118800

Frequently Asked Questions

Who can join the NCT06596187 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, studying SCI - Spinal Cord Injury. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06596187 currently recruiting?

Yes, NCT06596187 is actively recruiting participants. Contact the research team at yjchang@mail.cgu.edu.tw for enrollment information.

Where is the NCT06596187 trial being conducted?

This trial is being conducted at Taoyuan, Taiwan.

Who is sponsoring the NCT06596187 clinical trial?

NCT06596187 is sponsored by Chang Gung University. The trial plans to enroll 45 participants.

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