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Assessment of ADCY5-related Movement Disorders With Motion SENSors (SENSeo-ADCY5)

Primary Purpose

ADCY5-related Dyskinesia

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
caffeinated coffee - decaffeinated coffee
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for ADCY5-related Dyskinesia focused on measuring ADCY5, COFFEE, movement disorders

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ADCY5 mutation carriers
  • Age > 15 years old and 3 months
  • Informed consent from the patient or/ and a legal representative when appropriate
  • Affiliated with a social security system or beneficiary of such a regime or by waiver from CPP ( french ethic committee) for patients outside the European union ( EU)
  • daily caffeine consumer

Exclusion Criteria:

  • Hypersensitivity to caffeine or to xanthine derivatives
  • Heart condition contraindicating coffee intake
  • Liver failure
  • Impaired comprehension interfering with an informed consent
  • Positive pregnancy test for women of childbearing potential
  • Patient treated by Enoxacin, Ciprofloxacin, Norfloxacin (Noroxin), Cimetidine, Phenytoin β-adrenergic drugs (β2 mimetics) at inclusion.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    Caffeinated coffee

    Decaffeinated coffee

    Arm Description

    Drink caffeinated coffee one morning and drink decaffeinated coffee the other morning

    Drink decaffeinated coffee one morning and drink caffeinated coffee the other morning

    Outcomes

    Primary Outcome Measures

    Quantification movement disorders
    Assessment of correlation between displacement data using the ViconTM system and standardized clinical scales' scores of movements

    Secondary Outcome Measures

    Coffee effects
    Change in abnormal movements, measured with motion sensors (ViconTM system) after caffeinated coffee vs after decaffeinated coffee
    Involuntary scales evaluation
    Change in abnormal movements, measured with standardized clinical scale (Abnormal Involuntary Movement Scale (AIMS; Global score range 0 to 28 and severity subscore range 0 to 4; higher scores mean worse outcome), after caffeinated coffee vs after decaffeinated coffee
    Dyskinesia impairment evaluation
    Change in abnormal movements, measured with standardized clinical scale Dyskinesia Impairment Scale (DIS) (total score range 0 to 288; higher scores mean worse outcome) after caffeinated coffee vs after decaffeinated coffee
    Dyskinesia Rating Scale evaluation
    Change in abnormal movements, measured with standardized clinical scale Unified Dyskinesia Rating Scale (UDysRS) (total score range of 0 to 104; higher scores mean worse outcome), after caffeinated coffee vs after decaffeinated coffee

    Full Information

    First Posted
    April 29, 2021
    Last Updated
    November 26, 2021
    Sponsor
    Assistance Publique - Hôpitaux de Paris
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05136495
    Brief Title
    Assessment of ADCY5-related Movement Disorders With Motion SENSors
    Acronym
    SENSeo-ADCY5
    Official Title
    Assessment of ADCY5-related Movement Disorders With Motion SENSors: a Feasibility Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2021
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 12, 2022 (Anticipated)
    Primary Completion Date
    January 12, 2024 (Anticipated)
    Study Completion Date
    January 12, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Assistance Publique - Hôpitaux de Paris

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    ADCY5-related movement disorders are caused by dominant mutations in the ADCY5 gene. This rare neurogenetic disease is characterized by childhood-onset generalized hyperkinetic movements. Currently, the only tools available to rate the severity of movement disorders observed in ADCY5-patients are clinical rating scales of abnormal movements. These scales use the investigators' judgement to rate globally the severity of movements observed in various body parts of the patient. This protocol proposes to investigate a multimodal approach, combining a clinical scale assessment with ViconTM's objective movement measurement. A secondary objective of the study is to assess the effect of coffee on ADCY5-patients.
    Detailed Description
    ADCY5-related movement disorders are caused by dominant mutations in the ADCY5 gene. This rare neurogenetic disease is characterized by childhood-onset generalized hyperkinetic movements. The abnormal movements typically comprise a combination of dystonia, myoclonus and chorea occurring on a background of axial hypotonia, with superimposed disabling episodes of paroxysmal dyskinesia. The causing mutations are located in the ADCY5 gene coding for the Adenylate Cyclase 5 (AC5). AC5 is highly expressed in the striatal projection neurons of the striatum, a region involved in the control of movements. No effective treatment has been found. Currently, the only tools available to rate the severity of movement disorders observed in ADCY5-patients are clinical rating scales of abnormal movements. These scales use the investigators' judgement to globally rate movements severity in various body parts. This leads to inter-raters' scoring variability. An objective assessment through refined and comprehensive quantification of movements is needed. A motion capture system, such as ViconTM, could better reflect the global and focal variations of abnormal movements. This would be critical for the evaluation of responses to potential treatments. This protocol proposes to investigate a multimodal approach, combining a clinical scale assessment with ViconTM's objective movement measurement. A secondary objective of the study is to assess the effect of coffee on ADCY5-patients. The caffeine contained in coffee acts as a nonselective adenosine receptor antagonist, with a strong affinity for A2A receptors. By blocking A2A receptors, caffeine reduces the enzymatic activity of the altered mutated AC5 protein coded by the mutated ADCY5 gene. This effect could modulate the abnormal movements observed in patients.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    ADCY5-related Dyskinesia
    Keywords
    ADCY5, COFFEE, movement disorders

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    10 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Caffeinated coffee
    Arm Type
    Experimental
    Arm Description
    Drink caffeinated coffee one morning and drink decaffeinated coffee the other morning
    Arm Title
    Decaffeinated coffee
    Arm Type
    Experimental
    Arm Description
    Drink decaffeinated coffee one morning and drink caffeinated coffee the other morning
    Intervention Type
    Other
    Intervention Name(s)
    caffeinated coffee - decaffeinated coffee
    Intervention Description
    Drink caffeinated coffee one morning and drink decaffeinated coffee the other morning
    Primary Outcome Measure Information:
    Title
    Quantification movement disorders
    Description
    Assessment of correlation between displacement data using the ViconTM system and standardized clinical scales' scores of movements
    Time Frame
    24 HOURS
    Secondary Outcome Measure Information:
    Title
    Coffee effects
    Description
    Change in abnormal movements, measured with motion sensors (ViconTM system) after caffeinated coffee vs after decaffeinated coffee
    Time Frame
    24 Hours
    Title
    Involuntary scales evaluation
    Description
    Change in abnormal movements, measured with standardized clinical scale (Abnormal Involuntary Movement Scale (AIMS; Global score range 0 to 28 and severity subscore range 0 to 4; higher scores mean worse outcome), after caffeinated coffee vs after decaffeinated coffee
    Time Frame
    24 Hours
    Title
    Dyskinesia impairment evaluation
    Description
    Change in abnormal movements, measured with standardized clinical scale Dyskinesia Impairment Scale (DIS) (total score range 0 to 288; higher scores mean worse outcome) after caffeinated coffee vs after decaffeinated coffee
    Time Frame
    24 Hours
    Title
    Dyskinesia Rating Scale evaluation
    Description
    Change in abnormal movements, measured with standardized clinical scale Unified Dyskinesia Rating Scale (UDysRS) (total score range of 0 to 104; higher scores mean worse outcome), after caffeinated coffee vs after decaffeinated coffee
    Time Frame
    24 Hours

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    15 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: ADCY5 mutation carriers Age > 15 years old and 3 months Informed consent from the patient or/ and a legal representative when appropriate Affiliated with a social security system or beneficiary of such a regime or by waiver from CPP ( french ethic committee) for patients outside the European union ( EU) daily caffeine consumer Exclusion Criteria: Hypersensitivity to caffeine or to xanthine derivatives Heart condition contraindicating coffee intake Liver failure Impaired comprehension interfering with an informed consent Positive pregnancy test for women of childbearing potential Patient treated by Enoxacin, Ciprofloxacin, Norfloxacin (Noroxin), Cimetidine, Phenytoin β-adrenergic drugs (β2 mimetics) at inclusion.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    louise laure MARIANI, MD, PhD
    Phone
    1 42 16 27 48
    Ext
    +33
    Email
    louise-laure.mariani@icm-institute.org

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Assessment of ADCY5-related Movement Disorders With Motion SENSors

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