Home-Based Automated Therapy of Arm Function After Stroke Via Tele-Rehabilitation
2 other identifiers
interventional
25
1 country
1
Brief Summary
Constraint-Induced Movement therapy, also known as CI therapy, is an approach to physical rehabilitation derived from basic behavioral and neuroscience research. It has been shown to be efficacious for rehabilitating use of the more-affected arm in individuals more than one year after stroke with mild to moderate motor impairment. The first component of the therapy is intensive training in use of the more-affected arm on functional tasks for 3 hours daily for 10 consecutive weekdays. The second is wearing a protective safety mitt on the less-affected hand for all waking hours of the approximately 2-week treatment period that it is safe to do so. The purpose of the mitt is to discourage use of the less-affected arm. The third is a group of behavioral techniques designed to transfer gains from the treatment setting to the real world, which takes a therapist, on average, 30 minutes to implement on each treatment day. The purpose of this project is to develop and test a method for automating the delivery of this efficacious treatment in a way that the therapy can be provided in stroke patients' homes. After developing an automated CI therapy workstation that has tele-health capabilities, the investigators will conduct a randomized controlled trial to evaluate whether CI therapy delivered in the home using this workstation with remote supervision by a therapist via an Internet-based audiovisual link provides outcomes that are just as good as CI therapy delivered by a "live" therapist.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable stroke
Started Jun 2010
Longer than P75 for not_applicable stroke
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2010
CompletedFirst Submitted
Initial submission to the registry
June 17, 2010
CompletedFirst Posted
Study publicly available on registry
July 5, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2018
CompletedSeptember 28, 2018
September 1, 2018
3.2 years
June 17, 2010
September 26, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Motor Activity Log (MAL) Arm Use Scale at 2 weeks
Well-validated structured interview that assesses how much and how well the more-affected arm after stroke has been used to accomplish everyday activities over a specified period.
Baseline to 2 weeks (average)
Secondary Outcomes (3)
Change in Wolf Motor Function Test (WMFT) Performance Rate at 2 weeks
Baseline to 2 weeks (average)
Change in MAL Arm Use Scale at 6 months
Baseline to 6 months (average)
Change in MAL Arm Use Scale at 12 months
Baseline to 12 months (average)
Study Arms (2)
CI therapy
ACTIVE COMPARATORTele-AutoCITE
EXPERIMENTALAutoCITE stands for Automated Constraint Induced Therapy Extender.
Interventions
CI therapy is a behavioral approach to physical rehabilitation that has three components: 1. intense training of the more affected arm for several hours daily for multiple consecutive days, 2. restraint of the less affected arm during training hours and afterwards during the treatment period, 3. A package of behavioral techniques designed to transfer gains from the treatment setting to daily life. In this trial, CI therapy will be administered for 3 1/2 hours per day for 10 consecutive weekdays.
Eligibility Criteria
You may qualify if:
- more than 1 year after stroke
- some ability to voluntarily open fingers on more affected side of body
- some ability to voluntarily raise wrist on more affected side of body
- ability to stand independently for two minutes
- ability to transfer from sit to stand independently
You may not qualify if:
- serious, concurrent medical conditions including frailty
- excessive spasticity (high muscle tone) in more affected arm
- impairment in thinking that makes compliance with study activities difficult
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Alabama at Birmingham
Birmingham, Alabama, 35294, United States
Related Publications (1)
Taub E, Uswatte G, Pidikiti R. Constraint-Induced Movement Therapy: a new family of techniques with broad application to physical rehabilitation--a clinical review. J Rehabil Res Dev. 1999 Jul;36(3):237-51.
PMID: 10659807BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gitendra Uswatte, PhD
Psychology Department, University of Alabama at Birmingham
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor of Psychology
Study Record Dates
First Submitted
June 17, 2010
First Posted
July 5, 2010
Study Start
June 1, 2010
Primary Completion
August 1, 2013
Study Completion
August 1, 2018
Last Updated
September 28, 2018
Record last verified: 2018-09