ClinicalTrials.Veeva

Menu

Efficacy Research of Bimanual Intensive Training in Children With Hemiplegic Cerebral Palsy

National Taiwan University logo

National Taiwan University

Status

Enrolling

Conditions

Cerebral Palsy

Treatments

Other: Camp-based bimanual intensive training(BIT)

Study type

Interventional

Funder types

Other

Identifiers

NCT04516876
202004060RIND

Details and patient eligibility

About

This research project aims to investigate the feasibility, efficacy, and acceptability of camp-based model of BIT.

Enrollment

30 estimated patients

Sex

All

Ages

5 to 12 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. Diagnosis of cerebral palsy(CP) with one or more affected sides.
  2. Considerable nonuse of the affected upper limb (amount-of-use score of the Pediatric Motor Activity Log < 2.5).
  3. No excessive muscle tone (Modified Ashworth Scale ≤ 2 at any joints of the upper limb) before beginning treatment.
  4. No severe cognitive, visual, or auditory disorders according to medical documents, parental reports, and the examiner 's clinical observation.
  5. No injections of botulinum toxin type A or operations on the upper limb within 6 months.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Camp-based bimanual intensive training(BIT)
Experimental group
Treatment:
Other: Camp-based bimanual intensive training(BIT)

Trial contacts and locations

1

Loading...

Central trial contact

Tien-Ni Wang, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems