- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01422278
Rehabilitation of Conversion Gait Disorder
August 22, 2011 updated by: Annika A. Jordbru, Oslo University Hospital
Patients With Conversion Gait Disorder - Effect on Treatment and Common Gait Patterns. Randomized Clinical Trial
Evaluating the effects in functional status after three weeks of cognitive - and behavioural rehabilitation on patients with gait disorder.
The patients are followed up as after 1 and 12 months to study if any improvement is still present.
The patients are being recruited from neurological units.
The intervention is explanation of symptoms, positive reinforcement of normal behaviour and absence reinforcement of dysfunctional behaviour.
In addition the study aims at describing typical gait patterns at patients with gait disorder by using biomechanical measurements (EKG).
Study Overview
Detailed Description
Patients are being recruited from neurological unit/ div and out patients department of SSR and are randomized to treatment or control group.
Essential gait disorders do to conversion symptoms and willingness to participate in either of the two groups with informed consent are required.
Study Type
Interventional
Enrollment (Anticipated)
60
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Vestfold
-
Stavern, Vestfold, Norway, 3290
- Vestfold Hospital Trust, clinic physical medicine and rehabilitation
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 69 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- To determine the changes in functional status after three weeks of multidisciplinary rehabilitation in patients with conversion walking disorder.
Exclusion Criteria:
- Essential gait disorders do to conversion symptoms and willingness to participate in either of the two groups with informed consent are required.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in gait patterns
Time Frame: three weeks
|
three weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Improved life quality
Time Frame: 12 months
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Georg Høyer, DH, National committees for research ethics in Norway" for REK
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2007
Primary Completion (Actual)
September 1, 2010
Study Completion (Anticipated)
December 1, 2011
Study Registration Dates
First Submitted
January 16, 2006
First Submitted That Met QC Criteria
August 22, 2011
First Posted (Estimate)
August 23, 2011
Study Record Updates
Last Update Posted (Estimate)
August 23, 2011
Last Update Submitted That Met QC Criteria
August 22, 2011
Last Verified
August 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2.2004.164
- SSR.2005.1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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