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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02994719
Other study ID # 2015P000310
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2016
Est. completion date June 20, 2025

Study information

Verified date April 2024
Source Beth Israel Deaconess Medical Center
Contact Veronique Vanderhorst, MD PhD
Phone 617-667-0519
Email vvanderh@bidmc.harvard.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate whether speed-dependent measures of gait can be identified in patients with neurological conditions that affect gait, particularly in subjects with parkinsonian disorders.


Description:

This study aims to determine whether the gait patterns in these subjects differ in predictable and quantifiable ways from those of age- and sex-matched healthy controls. This will be conducted by asking 40 Parkinsonian disorder subjects and 40 age-matched healthy control subjects to walk 9 trials over an 18 ft walkway embedded with pressure sensors at baseline, self-selected slower and faster speeds. In addition, the protocol aims to investigate whether clusters of gait patterns can be identified within subgroups of individuals with parkinsonian disorders with varying co-morbidities or treatment conditions as well as patients with ataxia syndromes. For this aim an additional 20 Parkinsonian disorder subjects need to be recruited. Patients with parkinsonism as defined by UK PD Brain Bank Criteria (n=60), subjects with acquired or inherited ataxic syndromes (n=10) and age- and sex matched controls (n=40) will be recruited. There is an optional second visit in the protocol during which approximately 20 subjects with Parkinsonian disorders, who are willing to come off antiparkinson medication and if applicable, off both medication and deep brain stimulation, are asked to walk an additional 9 trials.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date June 20, 2025
Est. primary completion date June 20, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Age 18-85 (for both healthy and affected subjects). - Presence of at least 2 of the following: bradykinesia, rest tremor, rigidity, postural instability (UK PD Brain Bank Criteria) (Affected subjects only). - Montreal Cognitive Assessment will be employed to determine whether subjects will need the assent of a legally authorized representative. Subjects with MOCA = 21 will be consented only with the assent of the subject and informed consent of the authorized legal representative (Affected subjects only). - These may include subjects who may have indeterminate parkinsonism, when it is not clear whether they have idiopathic Parkinson's Disease versus one of the Atypical Parkinsonisms, such as Vascular Parkinsonism, Multiple System Atrophy, Progressive Supranuclear Palsy, Normal Pressure Hydrocephalus or Corticobasal Degeneration (Affected subjects only). - Subjects with assistive devices will be eligible for the study and may use them during the study (Affected subjects only). - Absence of complaints regarding difficulty walking such as arthritic pain, fatigue during walking or slowness of walking (Healthy subjects only). Exclusion Criteria: - Presence of alternative explanation for parkinsonism such as head trauma, drug-induced parkinsonism (affected subjects only). - Currently being treated for major medical illness requiring recent hospitalization (<14 days) (for both healthy and affected subjects). - Currently participating in another clinical study with an intervention arm (for both healthy and affected subjects). - Inability to consent due to cognitive impairment and absence of legally authorized representative (for both healthy and affected subjects). - Subjects with any cardiac, pulmonary conditions (congestive heart failure requiring hospitalization within the past 90 days, recent myocardial infarction < 90 days, supplemental oxygen-requiring subjects due to cardiac or pulmonary conditions) that limit their ability to safely participate in a walking trial (for both healthy and affected subjects).

Study Design


Intervention

Drug:
Anti-Parkinson medication
During the optional second visit subjects with neurological disease and already on anti-parkinson medication are asked to come off their anti-parkinson medication.
Device:
Deep Brain Stimulation
During the optional second visit subjects with neurological disease already treated with deep brain stimulation are asked to come temporarily stop deep brain stimulation and resume stimulation, with walking trials done in each condition.

Locations

Country Name City State
United States Clinical Research Center BIDMC Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Beth Israel Deaconess Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gait speed Method of assessment: physiological parameter through study completion, an average of 1 year
Secondary Swing duration Method of assessment: physiological parameter through study completion, an average of 1 year
Secondary Stance duration Method of assessment: physiological parameter through study completion, an average of 1 year
Secondary Cadence Method of assessment: physiological parameter through study completion, an average of 1 year
Secondary Stride length Method of assessment: physiological parameter through study completion, an average of 1 year
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