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Musical Biofeedback for Sensorimotor Control Capacity of Hands

Multisensory Biofeedback With Musical Interface for Sensorimotor Control Capacity of Hands

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04802564
Enrollment
73
Registered
2021-03-17
Start date
2021-03-15
Completion date
2025-06-11
Last updated
2025-08-21

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

Conditions

Hand Injuries

Keywords

musical biofeedback, auditory, vibrotactile stimulation

Brief summary

In the proposed study, the investigators assumed that music support treatment, a multisensory-based framework for ameliorating brain plasticity, combined with low-amplitude vibration stimulation can prime motor system and change in motor performance for the patient with a peripheral injury or the loss of a limb. The specific aim of this study is to develop a Multisensory Biofeedback with Musical Interface system, with the aim of improving the sensorimotor impairment of patients' hands.The expected outcomes of this research are to clarify the effects of application Multisensory Biofeedback with Musical Interface on motor and hand function for patients with hand injuries.

Interventions

OTHERregular hand therapy

edema control, scar management, stretching regimen, tendon gliding exercise, blocking exercise, muscle strengthening protocols

Sponsors

National Cheng-Kung University Hospital
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* tendon and bone injury in hand, wrist, and forearm; peripheral nerve injury in upper extremity; replantation; a combination of nerve and tendon or vascular injury; the protective sensation of the hand is absent or impaired

Exclusion criteria

* patients with deficits in cognition, perception or language comprehension, as well as severe pain and swelling in the upper limbs

Design outcomes

Primary

MeasureTime frame
Change in the result of pinch-holding-up-activity test8 weeks, 12 weeks and 24 weeks

Secondary

MeasureTime frame
Change in the result of Minnesota manual dexterity test8 weeks, 12 weeks and 24 weeks
Change in the result of Manual ability measurement4 weeks, 8 weeks, 12 weeks and 24 weeks
Change in the result of Near-Infrared Spectroscopy4 weeks and 12 weeks
Change in the result of Purdue pegboard test8 weeks, 12 weeks and 24 weeks
Chang in the result of active range of motion test4 weeks, 8 weeks, 12 weeks and 24 weeks
Chang in the result of two-point discrimination (S2PD) test4 weeks, 8 weeks, 12 weeks and 24 weeks
Chang in the result of Semmes-Weinstein monofilament (SWM) test4 weeks, 8 weeks, 12 weeks and 24 weeks

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026