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Study of Modified Constraint-Induced Aphasia Therapy Schedule to Treat Patients Following Sub-acute Stroke

NCT01625676 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2012-06-21

No results posted yet for this study

Summary

The purpose of this study is to assess the feasibility of modified Constraint-Induced Aphasia Therapy (CIAT) in the early sub-acute stage and to examine the efficacy of modified CIAT versus standard treatment with the same intensity of intervention.

Conditions

  • Aphasia

Interventions

OTHER

Investigate efficacy of modified ciat schedule

2 hours of training over 15 days

OTHER

examine the efficacy of standard treatment versus modified ciat schedule

2 hours of training over 15 days

Sponsors & Collaborators

  • NRZ Magdeburg Median Kliniken GmbH & Co

    lead OTHER

Principal Investigators

  • Almut A Sickert, PhD · NRZ Median Klinik Magdeburg

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
34 Years
Max Age
84 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-08-31
Primary Completion
2010-10-31
Completion
2011-12-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01625676 on ClinicalTrials.gov