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
About this trial
This is an interventional other trial for ADCY5-related Dyskinesia focused on measuring ADCY5, COFFEE, movement disorders
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.
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
NCT ID
NCT05136495
First Posted
April 29, 2021
Last Updated
November 26, 2021
Sponsor
Assistance Publique - Hôpitaux de Paris
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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