NCT07351877Recruiting
Precision Vibration Therapy for Neuromuscular and Functional Improvement in Older Adults and Stroke Survivors
Exploring the Clinical Benefits of Precision Vibration on Neuromuscular Induction, Proprioceptive Gain, Functional Enhancement, and Pain Relief in Older Adults and and Stroke Survivors
Source: ClinicalTrials.gov · Last updated 20 Jan 2026
Brief summary (registry, in English)
To address muscle weakness, sensory degradation, functional decline, and pain caused by geriatric syndromes in older adults and stroke survivors, this project proposes a series of studies aimed at improving neuromuscular performance, muscle strength, proprioceptive gain, functional outcomes, and pain relief through the use of a precise vibration system. In the first phase, a vibration exercise system will be implemented to recruit frail older adults and older adults with stroke for clinical trials. The goal is to verify the benefits of vibration intervention on limb muscle strength, proprioception, and movement function. In the third phase, quantitative pain assessments and related scales will be used to evaluate chronic pain thresholds and affected regions in older adults and stroke survivors, and to validate the effectiveness of vibration intervention in alleviating their pain.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- First submitted
- 29 Dec 2025
- Start date
- 18 Sept 2024
- Primary completion date
- 18 Dec 2027
- Lead sponsor
- National Health Research Institutes, Taiwan
- Diseases
- Stroke
- NCT number
- NCT07351877
What you commit to
- Study type: Interventional
- Planned participants: 80
- From 18 Sept 2024 to the primary completion date, 18 Dec 2027
- 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
- Concomitant vestibular or cerebellar disorders that severely impair motor performance
Other illness
- History of surgery on the upper or lower limbs within the past 6 months
- Stroke Survivors:
- Recurrent stroke during the current episode (i.e., acute re-stroke) or otherwise clinically unstable stroke presentation
- Cognitive impairment attributable to stroke that precludes effective communication or adherence to the study protocol
- Other neurological or psychiatric disorders judged likely to interfere with motor performance or study outcomes
Other
- Older Adults:
- Acute or chronic neurological injury involving the upper or lower limbs within the past 6 months
- Acute or chronic musculoskeletal injury involving the upper or lower limbs within the past 6 months
- Markedly elevated spasticity preventing isolated voluntary movement of the target limb (MAS score ≥ 3)
- Hemianopsia or severe hemineglect that significantly interferes with task execution
- Orthopedic or traumatic comorbidities causing significant pain or limiting safe participation during evaluation or intervention
Who the study is looking for
- Older Adults:
- Meet two or more criteria of the Study of Osteoporotic Fractures (SOF) frailty index
- Willing to participate in the study and comply with all study procedures
- Able to wear and safely use the vibration device
- Normal cognitive function (Mini-Mental State Examination \[MMSE\] score ≥ 23)
- Presence of knee joint pain in the lower limbs
- Stroke Survivors:
- Clinical diagnosis of ischemic or hemorrhagic stroke confirmed by a physician
- Clinically stable stroke condition (i.e., not in an acute or unstable phase)
- Brunnstrom stage ≥ III for the affected limb
- Cognitive ability sufficient to follow study procedures (MMSE score ≥ 23)
- Modified Ashworth Scale (MAS) score \< 3 for the paretic limb
- Able to sit safely and participate in vibration or rehabilitation sessions for up to 60 minutes per visit
- Willing and able to comply with all study procedures and provide written informed consent
Age in the registry: 18 years to 95 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 |
|---|---|---|---|
| National Center for Geriatrics and Welfare Research, National Health Research Institutes Coordinator of this site? Confirm its status | Taipei | Taiwan | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.