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CompletedNCT00991692Updated Oct 8, 2009

A Multisite Trial of ACQUIREc Therapy

An interventional study of Therapy services (ACQUIREc Therapy) in Hemiparetic Cerebral Palsy, sponsored by University of Alabama at Birmingham. Completed at 1 site in United States. Open to participants aged 3 Years to 8 Years. Per ClinicalTrials.gov, last updated 2009-10-08.

Sponsored by University of Alabama at Birmingham · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
18
Allocation
Randomized
Ages
3 Years to 8 Years
Sex
All
01

Study 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.

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Conditions studied

  • Hemiparetic Cerebral Palsy

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Keywords

  • Pediatric CI Therapy
  • ACQUIREc Therapy
  • Dosage
  • Occupational Therapy
  • Physical Therapy
  • Cerebral Palsy
  • Hemiparesis
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In context

Cerebral Palsy

1,853 studies on the registry are indexed under Cerebral Palsy; 435 are open to participants now.

This study's enrollment of 18 is below the median of 33 across 1,368 interventional studies indexed under Cerebral Palsy.

Browse Cerebral Palsy studies →

Lead sponsor

University of Alabama at Birmingham is the lead sponsor of 1,396 studies on the registry; 284 are open to participants now.

Of its 156 completed or terminated interventional studies of FDA-regulated products, 124 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
3 Years to 8 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Children 3-6 years of age
  • Hemiparetic CP

Exclusion criteria

Exclusion Criteria:

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

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Single (Outcomes assessor)
Enrollment
18 participants (actual)

Study arms

  • Experimental
    Treatment dosage levels examined

    Other: Therapy services (ACQUIREc Therapy)

Interventions

  • OtherTherapy services (ACQUIREc Therapy)

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

    Also known as: Occupational Therapy, Physical Therapy, Pediatric CI Therapy, ACQUIREc Therapy

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Study locations

1 site
  • University of Alabama at Birmingham
    Birmingham, Alabama 35124, United States
07

References and documents

Publications

  • DeLuca SC, Case-Smith J, Stevenson R, Ramey SL. Constraint-induced movement therapy (CIMT) for young children with cerebral palsy: effects of therapeutic dosage. J Pediatr Rehabil Med. 2012;5(2):133-42. doi: 10.3233/PRM-2012-0206. PubMed 22699104 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 8, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00991692
Lead sponsor
University of Alabama at Birmingham
First posted
Oct 8, 2009
Start date
Jun 2008
Primary completion
Aug 2009
Completion
Oct 2009
Last update
Oct 8, 2009

Study contacts

Stephanie C DeLuca, PhD
principal investigator · University of Alabama at Birmingham

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2009. You cannot join it, but the record below documents what was studied.

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