Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00057018 · ClinicalTrials.gov registry record · Phase 3

Improving Arm Mobility and Use After Stroke

A Phase 3 study of Cerebrovascular Accident, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

Completed
Registry status
Phase 3
Development phase
229
Enrollment target
7
Study locations

NCT00057018: Completed Phase 3 study of Cerebrovascular Accident, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

NCT00057018 is a Phase 3 study of Cerebrovascular Accident that has completed, run by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). The registered enrollment target is 229 participants, below the 509-participant average among 26 other Cerebrovascular Accident trials with a reported enrollment target (55% lower). The trial reports 7 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00057018, a Phase 3 study of Cerebrovascular Accident, has completed, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

COMPLETED
Registry status
Phase 3
Development phase
229 participants
Enrollment target
7
Study locations

Study Summary

An individual suffering a stroke or other brain injury may lose function on one side of the body (partial paralysis). As the individual shifts activities to favor the unaffected side, the problem worsens. Constraint induced (CI) therapy forces the individual to use the neglected arm by restraining the good arm in a sling. This study examines the effectiveness of CI therapy for improving arm motion after stroke.

Conditions Studied

Interventions

  • PROCEDURE Constraint-induced movement therapy

Study Locations (7)

North Carolina

  • University of North Carolina at Chapel Hill - Chapel Hill
  • Wake Forest University School of Medicine - Winston-Salem

Alabama

  • University of Alabama at Birmingham - Birmingham

California

  • University of Southern California - Los Angeles

Florida

  • University of Florida - Gainesville

Georgia

  • Emory University - Atlanta

Ohio

  • Ohio State University - Columbus

Trial Details

FieldValue
Enrollment Target 229 participants
Start Date 2000-04
Est. Completion 2006-01
Phase Phase 3

What the finished NCT00057018 record still lists

NCT00057018 is an interventional study that assigns participants to a tested intervention. The registered 229 participants enrollment target is mid-sized for trials with a published cap, below the 509-participant average among 26 other Cerebrovascular Accident trials with a reported enrollment target (55% lower).

The record links to 1 condition, with Cerebrovascular Accident appearing as the primary indexed condition, and to 1 intervention - of which Constraint-induced movement therapy is the first listed.

NCT00057018 lists 7 locations in 6 states (North Carolina, Alabama, California).

Frequently Asked Questions

What is clinical trial NCT00057018 about?

NCT00057018 is a clinical study titled "Improving Arm Mobility and Use After Stroke". An individual suffering a stroke or other brain injury may lose function on one side of the body (partial paralysis). As the individual shifts activities to favor the unaffected side, the problem worsens. Constraint induced (CI) therapy forces the individual to use the neglected arm by restraining t...

What is the current status of trial NCT00057018?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 229 participants. The study started on 2000-04. Estimated completion is 2006-01.

What conditions does trial NCT00057018 study?

This clinical trial studies the following conditions: Cerebrovascular Accident.

What interventions are being tested in trial NCT00057018?

The interventions under investigation include: Constraint-induced movement therapy (PROCEDURE).

Who is sponsoring clinical trial NCT00057018?

This trial is sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), which has 305 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00057018 being conducted?

This trial has 7 study locations across Alabama, California, Florida, Georgia, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Cerebrovascular Accident

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00057018's enrollment target sits among peer trials

229 6th of 26 higher than 21 of 26 other Cerebrovascular Accident trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cerebrovascular Accident trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02710253 · 230 participants · Phase 2

    Salvage Radiation Therapy in Treating Patients With Metastatic Cancer That Has Progressed After Systemic Immunotherapy

  • NCT02777879 · 230 participants

    Lung Microbiome and Inflammation in Early COPD

  • NCT03824483 · 230 participants · Phase 2

    Study of Zanubrutinib, Obinutuzumab, and Venetoclax in Patients With Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Leukemia (SLL)

  • NCT03833622 · 230 participants · NA

    Shared Decision Making to Improve Goals of Care in the ED

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00057018, the US trial registry maintained by the National Library of Medicine. NCT00057018 (mid enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.