ClinicalTrials.Veeva

Menu

A Multisite Trial of ACQUIREc Therapy

The University of Alabama at Birmingham logo

The University of Alabama at Birmingham

Status

Completed

Conditions

Hemiparetic Cerebral Palsy

Treatments

Other: Therapy services (ACQUIREc Therapy)

Study type

Interventional

Funder types

Other

Identifiers

NCT00991692
deluca-ms1

Details and patient eligibility

About

A multisite trial to testing different dosage levels of a systematic form of Pediatric Constraint-Induced (CI) Therapy called ACQUIREc Therapy. The high dosage treatment involved 6 hours of daily therapy services for 21 days. This was compared to a moderate dosage level of 3 hours of daily therapy services for 21 days. It was hypothesized that children receiving the higher therapy dosage would have greater and more clinically significant benefits from ACQUIREc Therapy but that both groups of children would benefit from the therapy services.

Enrollment

18 patients

Sex

All

Ages

3 to 8 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children 3-6 years of age
  • Hemiparetic CP

Exclusion criteria

  • No prior CI therapy treatments
  • No Botox for 6-months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

18 participants in 1 patient group

Treatment dosage levels examined
Experimental group
Treatment:
Other: Therapy services (ACQUIREc Therapy)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems