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NCT03307161 Clinical Trial

Osteopathic Manual Treatment Parkinson's Disease and Truncal Dystonia

Parkinson Disease Clinical Trial

Official title:
Osteopathic Manual Treatment of Postural Abnormality, Pain, and Autonomic Control of Cardiac Function in People With Parkinson's Disease and Truncal Dystonia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03307161
Other study ID # 1130
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 2016
Est. completion date September 20, 2021

Study information
Verified date September 2021
Source New York Institute of Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will determine if posture and heart rate variability will significantly improve in Parkinsons disease with camptocormia after osteopathic manual treatments dystonia.

Description:

This study will determine if posture and heart rate variability will significantly improve in Parkinsons disease with camptocormia after receiving 8-weekly sessions of the osteopathic manual treatments for truncal flexion dystonia as measured by the distance of the external acoustic meatus from a plumb-line to lateral malleolus, spinal X ray, and heart rate variability.

Recruitment information / eligibility
Status Completed
Enrollment 10
Est. completion date September 20, 2021
Est. primary completion date September 20, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Parkinson's disease; able to stand for three minutes or more Exclusion Criteria: - severe dementia, moderate or severe hallucinations and psychosis; unable to stand for three minutes

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• osteopathic manual therapy
Investigators board certified in osteopathic manual therapy will use their hands in a non-invasive manner to improve dystonia symptoms

Locations
Country Name City State
United States New York Institute of Technology Old Westbury New York

Sponsors (1)
Lead Sponsor Collaborator
New York Institute of Technology

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary change in posture inches of forward head carriage 8 weeks
Primary change in heart rate variability heart rate changes 8 weeks
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