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NCT06452576 Clinical Trial

Use of Vibration During Constraint-induced Movement Therapy

Hemiparesis Clinical Trial

— CPT  

Official title:
Use of Vibration During Constraint-induced Movement Therapy

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06452576
Other study ID # Pro00137672
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 5, 2024
Est. completion date September 9, 2024

Study information
Verified date June 2024
Source Medical University of South Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether the hand function will improve more by using low-level vibration during constraint-induced movement therapy (CIMT), compared to CIMT alone without vibration.

Description:

The low-level vibration has been shown to increase therapy outcome when used as an adjunct to therapy in adults with hemiparesis. Children who participates in the CIMT camp at MUSC will be recruited to take part in the study. Participating children will wear a watch device on their weaker arm during CIMT. The watch will vibrate only for the children who were assigned to the treatment group.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 8
Est. completion date September 9, 2024
Est. primary completion date September 9, 2024
Accepts healthy volunteers No
Gender All
Age group 4 Years to 9 Years
Eligibility Inclusion Criteria: - Unilateral upper limb motor weakness - Can use the affected upper limb as a gross assist during play and self-care activities - Ambulatory for their age with intact balance and protective reactions in the less involved upper limb. Exclusion Criteria: - Developmental delays limiting spontaneous use of the affected upper limb - Other health impairment

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Vibration
Watch vibrates.
Behavioral:
• constraint-induced movement therapy
A splint or mitt is placed on the stronger, unaffected hand to encourage use of the affected upper limb in therapy.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Medical University of South Carolina

Outcome
Type Measure Description Time frame Safety issue
Primary Box and Block Test number of blocks moved in a minute pre-therapy and post-therapy, up to 5 consecutive days
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