Gait Training for Persons With Stroke (GTS)
This study has been completed.
Sponsor:
University of Aarhus
Information provided by:
University of Aarhus
ClinicalTrials.gov Identifier:
NCT00612300
First received: January 28, 2008
Last updated: February 16, 2010
Last verified: February 2010
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Purpose
The objective of this study is to investigate the effects of an automatic gait trainer (Lokomat) handled by physical therapists compared with categorized gait training by physical therapists in ambulatory stroke patients. Gait speed, gait distance and gait symmetry are used to evaluate study effects.
Hypotheses: 1) The Lokomat improves stroke patients gait speed, distance and symmetry more than categorized gait training.
| Condition | Intervention | Phase |
|---|---|---|
|
Stroke Middle Cerebral Artery Infarction |
Behavioral: Lokomat - Physical therapy Behavioral: Physical therapy - Lokomat |
Phase 0 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Crossover Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | The Lokomat Gait Orthosis Compared to Categorized Gait Training by Physical Therapists in Patients Early Post Stroke |
Resource links provided by NLM:
Genetics Home Reference related topics:
cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
MedlinePlus related topics:
Methamphetamine
U.S. FDA Resources
Further study details as provided by University of Aarhus:
Primary Outcome Measures:
- 10 meters walking test (gait speed) [ Time Frame: at inclusion, week 3 and week 6 ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Six minutes walking test [ Time Frame: Inclusion, wek 3 and week 6 ] [ Designated as safety issue: No ]
- Gait symmetry index [ Time Frame: Inclusion, week 3 and week 6 ] [ Designated as safety issue: No ]
- Timed Up And Go [ Time Frame: Inclusion, Week 3 and Week 6 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 16 |
| Study Start Date: | June 2007 |
| Study Completion Date: | June 2009 |
| Primary Completion Date: | June 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: A-B
Gait training by an automatic gait trainer (Lokomat) for 3 weeks followed by 3 weeks of categorized gait training by a physical therapist
|
Behavioral: Lokomat - Physical therapy
A: Lokomat training, 30 minutes per day for 3 weeks, 5 days per week. B: Categorized gait training by physical therapist, 30 minutes per day for 3 weeks, 5 days per week
|
|
Experimental: B-A
Categorized gait training by physical therapists for 3 weeks followed by 3 weeks of lokomat training
|
Behavioral: Physical therapy - Lokomat
B: Daily 30 minutes of gait training with a physical therapist, 5 days per week for 3 weeks. A: Daily 30 minutes of Lokomat training, 5 days per week for 3 weeks. |
Eligibility| Ages Eligible for Study: | 30 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- First time Stroke
- Middle cerebral artery infarction
- Less than three month from stroke onset
- Able to walk with or without a stick at gait speed less than 0.5 m/s
- Participants are able to cope with the Lokomat
Exclusion Criteria:
- Co-morbidity which impedes study participations
- Language deficits which makes it impossible to understand oral or written study instructions
- More than 190 cm tall and 135 kg in weight
- Pregnancy
- No gait function prior stroke
- Skin sore or eruption on lower extremity or trunk, differences in lower extremity length of more than 2 cm or contracture of lower extremity which impedes gait training in the Lokomat -
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00612300
Locations
| Denmark | |
| Hammel Neurorehabilitation and Research Center | |
| Hammel, Denmark | |
Sponsors and Collaborators
University of Aarhus
Investigators
| Study Chair: | Jørgen F Nielsen, Professor | Hammel Neurorehabilitation and Research Center, Denmark |
| Study Director: | Carsten Kock-Jensen, MD | Hammel Neurorehabilitation and Research Center, Denmark |
| Principal Investigator: | John Brincks, PhD student | Hammel Neurorehabilitation and Reseach Center |
More Information
No publications provided
| Responsible Party: | John Brincks, PT, PhD student, Hammel Neurorehabilitation and Research Center |
| ClinicalTrials.gov Identifier: | NCT00612300 History of Changes |
| Other Study ID Numbers: | 2 |
| Study First Received: | January 28, 2008 |
| Last Updated: | February 16, 2010 |
| Health Authority: | Denmark: The Ministry of the Interior and Health |
Keywords provided by University of Aarhus:
|
Ambulatory stroke patients Gait training Lokomat Physical therapy |
Additional relevant MeSH terms:
|
Infarction Stroke Cerebral Infarction Infarction, Middle Cerebral Artery Ischemia Pathologic Processes Necrosis Cerebrovascular Disorders Brain Diseases |
Central Nervous System Diseases Nervous System Diseases Vascular Diseases Cardiovascular Diseases Brain Infarction Brain Ischemia Cerebral Arterial Diseases Intracranial Arterial Diseases |
ClinicalTrials.gov processed this record on May 19, 2013