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CompletedNCT02627664ProdDiGYParkUpdated May 18, 2017

Study of Dysarthria, Swallowing Disorders and Respiratory in Parkinson's Disease

An observational study in Parkinson's Disease, sponsored by University Hospital, Lille. Completed at 1 site in France. Open to participants aged 35 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-05-18.

Sponsored by University Hospital, Lille · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
70
Ages
35 Years to 80 Years
Sex
All
01

Study summary

The investigators prospectively enrolled 64 early PD patients (less than 3 years after the first symptom) in order to prospectively assess the natural history of non-dopaminergic symptoms.

Read the detailed description

Patients were evaluated at baseline and after 2 years in off drug condition. Clinical, psychological, neuropsychological evaluations, functional respiratory evaluation, swallowing video fluoroscopy, dysarthria, gait and axial disorders.

02

Conditions studied

  • Parkinson's Disease

Keywords

  • Idiopathic early
  • Parkinson's Disease
03

Who can participate

Ages eligible
35 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients with Parkinson's disease (PD) with early idiopathic ( ≤ 5 years of evolution )

Inclusion criteria

  • idiopathic parkinson's disease

Exclusion criteria

Exclusion Criteria:

  • dementia
  • severe axial gait disorders
  • respiratory or ENT pathology
  • Pregnancy
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
70 participants (actual)
Patient registry
No

Groups and cohorts

  • observational study

    natural history of non dopaminergic signs

    Other: observational study

Interventions

  • Otherobservational study

    natural history of non dopaminergic signs

05

What researchers measure

Primary outcomes

  1. dysarthria severity assessed by the BECD scale

    BECD (French battery of clinical evaluation of the dysarthria) is a validated scale for qualitative assessment of dysarthria severity in neurological disorders, especially PD

    Time frame: 2 years

Secondary outcomes

  1. respiratory insufficiency detection

    pulmonary function tests include spirometry with standard spirometer and maximal inspiratory and expiratory flow volume curves . At least 3 reproductible F-V curves are necessary. Values of FCV, FEV, peak expiratory flow, peak inspiratory flow, forced expiratory flow, SNIP were measured 12 hours after last levodopa intake (off drug)

    Time frame: 2 years

  2. swallowing function

    150 mL glass of water test video fluoroscopy of swallow in off drug condition face and profile incidences: qualitative analysis of oral, pharyngeal, aspiration if necessary blindly assessed by 2 ENT experts in PD

    Time frame: 2 years

  3. gait axial function (freezing)

    SWS test rhythmic tests for differens imposed frequencies (upper lower limb and facial) kinematic analysis of gait parameters by VICON (oxford metrics)

    Time frame: 2 years

  4. Mattis scale

    Time frame: 2 years

  5. LARS scale

    Time frame: 2 years

  6. MADRS scale

    Time frame: 2 years

  7. PAS scale

    Time frame: 2 years

  8. MoCA

    Time frame: 2 years

  9. Genetic Polymorphisme

    To evaluate of cognitive and profile correlation to the polymorphisms of COMT (catechol-O-methyltransferase: Val158Met COMT) of MAPT H1 / H2 (microtubule associated tau protein) and ApoE (Apolipoprotein-E-ε2, 3, 4 )

    Time frame: 2 years

06

Study locations

1 site
  • Francine Niset
    Lille, 59000, France
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT02627664
Lead sponsor
University Hospital, Lille
Collaborators
France Parkinson Association
Responsible party
Sponsor
First posted
Dec 11, 2015
Start date
Mar 2011
Primary completion
Feb 9, 2017
Completion
Feb 9, 2017
Last update
May 18, 2017

Study contacts

luc defebvre, MD PhD
study chair · CHRU LILLE FRANCE

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2017. You cannot join it, but the record below documents what was studied.

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