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A Multisite Trial of ACQUIREc Therapy

A Multisite Trial of ACQUIREc Therapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00991692
Enrollment
18
Registered
2009-10-08
Start date
2008-06-30
Completion date
2009-10-31
Last updated
2009-10-08

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

Conditions

Hemiparetic Cerebral Palsy

Keywords

Pediatric CI Therapy, ACQUIREc Therapy, Dosage, Occupational Therapy, Physical Therapy, Cerebral Palsy, Hemiparesis

Brief summary

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.

Interventions

OTHERTherapy services (ACQUIREc Therapy)

Dosage levels that are associated with the efficacy of intensive therapeutic services provided by OT and PT professionals.

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
3 Years to 8 Years
Healthy volunteers
No

Inclusion criteria

* Children 3-6 years of age * Hemiparetic CP

Exclusion criteria

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

Countries

United States

Outcome results

None listed

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