Cervical Dystonia Clinical Trial
Official title:
Effect of Osteopathic Manipulative Medicine on Motor Function and Quality of Life in Cervical Dystonia
NCT number | NCT02420106 |
Other study ID # | BHS-983 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | February 2014 |
Est. completion date | February 2019 |
Verified date | July 2019 |
Source | New York Institute of Technology |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the proposed research is to determine if Osteopathic manipulative medicine (OMM) used alone or in combination with the standard treatment of botulinum toxin intramuscular injections improves motor function and quality of life amongst people with cervical (neck) dystonia.
Status | Completed |
Enrollment | 10 |
Est. completion date | February 2019 |
Est. primary completion date | February 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 2 Years to 100 Years |
Eligibility |
Inclusion Criteria: - clinical diagnosis of cervical dystonia or spasmodic torticollis - ages 2-100 Exclusion Criteria: - no clinical diagnosis of cervical dystonia or spasmodic torticollis - symptoms beginning over the age of 40 - pregnant women are excluded from Aim 2 |
Country | Name | City | State |
---|---|---|---|
United States | New York Institute of Technology | Old Westbury | New York |
Lead Sponsor | Collaborator |
---|---|
New York Institute of Technology |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Motor Function | Motor function will be assessed by Vicon 3-Dimensional analysis of the subjects' biomechanics while walking and will depict stride length and arm swing on each side of the body as well as the posture of the shoulder and pelvic girdle with reference to the coronal, transverse and sagittal planes. | baseline and 5 weeks | |
Secondary | Change in Quality of Life | Quality of Life will be assessed by the CDIP-58 questionnaire | baseline and 5 weeks |
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