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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02207387
Other study ID # H13-02074
Secondary ID
Status Recruiting
Phase N/A
First received July 28, 2014
Last updated March 31, 2015
Start date October 2013
Est. completion date March 2017

Study information

Verified date March 2015
Source University of British Columbia
Contact Tammy Kang
Phone 604 822 9722
Email tammy.kang@ubc.ca
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

This study will investigate the effects of a contingency-based musical walking intervention program called Ambulosono on neural mechanisms in the brain. The investigators will investigate the long-term impact of Ambulosono on brain plasticity with functional MRI technique. Participants will undergo 3 months of Ambulosono training and their pre-training and post-training fMRI brain scans will be compared to understand the neural networks and brain mechanisms following this intervention. The investigators hypothesized that Ambulosono may induce functional compensatory reorganization of neural networks in the brain. This project will allow us to address the important potential confound of placebo influence and to aid in optimizing this intervention program. Additionally, the investigators are hoping to investigate the synergistic effects of rasagiline and exercise; the investigators' hypothesis is that there will be a positive synergistic effect, and that exercise will augment the effectiveness of rasagiline in treating Parkinson's symptoms.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date March 2017
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender Both
Age group 19 Years and older
Eligibility Inclusion Criteria:

- Over 19 years of age

- Confirmed diagnosis of Parkinson's Disease

- Can walk 5 to 10 minutes unassisted

- Have a safe place to walk (outdoor or indoor)

- Have mild to moderate Parkinson's disease (HY1-3)

- Be able to lay flat in the scanner for the period of the study

- No reliance on wheelchair or other walking aid for ambulation

- Absence of any other serious medical conditions such as hearing impairment and dementia

- No history of other neurological and psychiatric illnesses

- No recent musculoskeletal impairment or injuries that may prevent walking

Exclusion Criteria:

- Under 19 years of age

- Unconfirmed PD diagnosis

- Require walking aid, wheelchair-bound

- No access to safe walking pathway

- Severe PD (Hoehn & Yahr stages>3)

- Impaired hearing

- Atypical Parkinsonism

- Concurrent dementia

- Recent knee, hip or foot injury (need permission from doctor)

Exclusion Criteria for fMRI

- Pacemaker

- Brain aneurysm clip

- Cochlear implant

- Recent surgery within the past 6 weeks

- Possibility of pregnancy

- Electrical stimulator for nerves or bones

- Implanted infusion pump

- History of any eye injury involving metal fragments

- History of working with metals (grinding, machining, or welding)

- Artificial heart valve

- Orthopaedic hardware (artificial joint, plate, screws, rods)

- Other metallic prostheses

- Coil, catheter or filter in any blood vessel

- Ear or eye implant

- Recent tattoos within the past 6 weeks

- Shrapnel, bullets, or other metallic fragments

- Medication releasing skin patches (nicotine, birth control, nitroglycerine)

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Azilect
Rasagiline is Parkinson's medication that can be taken alone early in the disease or with other medication and is hypothesized to produce synergistic effects with exercise.
Behavioral:
Exercise
Walking and other forms of exercise have been seen clinically and in numerous research studies to be effective against Parkinson's symptoms.
Other:
Music


Locations

Country Name City State
Canada Pacific Parkinson's Research Centre Vancouver British Columbia

Sponsors (2)

Lead Sponsor Collaborator
University of British Columbia Teva Pharmaceutical Industries

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Changes in mood Beck's Inventory for Depression
Beck's Inventory for Anxiety
Parkinson Fatigue Scale
baseline and one month and four months No
Other Changes in impact/quality of life PDQ-39 Quality of Life Questionnaire baseline and one month and four months No
Primary Change from baseline in brain imaging signals (fMRI) resting state data task-evoked data cortical thickness volume sizes of specified brain structures one month and four months No
Secondary Change from baseline in motor symptoms of PD Motor Symptoms:
UPDRS-III scores
Time taken to perform TUG and One Leg Stand Balance Test
Gait performance observed from Line Walking Test, 6-Minute Walking Test, Coordinated Arm and Leg Swing Test
baseline and one month and four months No
Secondary Change from baseline in cognition of PD Cognition:
MOCA scores
Changes in reaction times (Simple Reaction Time Test, Trail Making Test A and B)
Performance on Phonemic Verbal Fluency Test
baseline and one month and four months No
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