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Development and Application of Portable Multisensory Stimulation Device

Development and Application of Portable Multisensory Stimulation Device: Vibroacustic Therapy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04005313
Enrollment
60
Registered
2019-07-02
Start date
2017-01-31
Completion date
2019-07-31
Last updated
2019-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Impairment

Keywords

Electromyographic activity, Neck pain, Electroencephalographic activity, dementia

Brief summary

This is a study to develop the vibroacustic devices, and to compare the effects between vibroacustic device therapy and music therapy in adults with dementia or with neck pain. The immediate effect and long-term training effect would be assessed.

Detailed description

The outcome measures included functional assessment ( such as: range of motion, balance etc.) and neurolphysiological assessment (such as: electroencephalographic activity or electromyographic activity).

Interventions

the participants will receive the vibroacustic device or music therapy

Sponsors

Buddhist Tzu Chi General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 95 Years
Healthy volunteers
Yes

Inclusion criteria

* mild to moderate Dementia * age-matched healthy subjects

Exclusion criteria

* can not follow order

Design outcomes

Primary

MeasureTime frameDescription
the electroencephalographic (EEG) activities ncluding Alpha, Beta, Theta, and Delta signals will be assessed in persons with mild to moderate dementia and healthy subjects.after sensory stimulation. .one yearThe EEG was recorded by EMOTIV EPOC+ mobile headset (Bioinformatics Company, USA). The wireless 14-EEG channels on the skull were located at anterior frontal (AF), frontal (F), frontal central (FC), temporal (T), parietal (P) and occipital (O) areas,The frequency analysis of brain waves includinh Alpha, Beta, Theta, and Delta signals before, during and after sensory stimulation will be recorded and analyzed.

Secondary

MeasureTime frameDescription
The pressure pain threshold following multisensory stimulation will be assessed around cervical region.one yearThe pressure pain threshold was measured by MicroFET3 ( Hoggan Health Industries, Utah, USA) at cervical region including cervical erector (CE), upper trapezius (UT) and sternocleidomastoid (SCM). At the trigger point of the muscle, the pressure of the test group is increased at a rate of about 1 newton/second. When the subject feels uncomfortable, the active stop is the end point of the test for perceived pain threshold.

Countries

Taiwan

Contacts

Primary ContactKwan-Hwa Lin, PhD
khlin03@mail.tcu.edu.tw0385653012499

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026