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Digital Solution to Improve Cognitive Function in Epilepsy: PRODDIGE Project (PRODDIGE)

Primary Purpose

Cognitive Change

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
cognitive rehabilitation
Sponsored by
Central Hospital, Nancy, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cognitive Change

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Person with epilepsy, according to Fisher et al. (2005) criteria: all type of epilepsy could be include (new-onset and drug-resistant)
  • Treatment must have been stable for 4 months: have the same molecule
  • Person who has received full information about the organization of the research and has not objected to his or her participation and the use of his or her data
  • Person aged 18 and over
  • Mandatory affiliation to a social security scheme
  • Validated cognitive inclusion criterion: having a YES response on the cognitive complaint questionnaire :

A.Spontaneous complaint :

Does the patient spontaneously complain of language difficulties?

B.Subjective complaint :

  1. Do you search for your words?
  2. Do you sometimes feel like you have the word on the tip of your tongue?
  3. Do you sometimes have trouble finding the names of people you know well?
  4. Do you ever say one word for another?

Exclusion Criteria:

  • Person with another neurological condition

Patients and normal control :

  • A person over the age of majority who is subject to a legal protection measure or who is unable to express their consent.
  • Person deprived of liberty by a judicial or administrative decision
  • A person who regularly uses psychoactive substances (cannabis, alcohol, etc.).

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Placebo Comparator

    No Intervention

    Arm Label

    "application supervised by a psychologist via teleconsultations"

    "application in total autonomy"

    "control" group without using the application

    Arm Description

    patient have app, and teleconsultation with psychologist

    patients have app, they play when they want

    patients haven't app

    Outcomes

    Primary Outcome Measures

    Number of weekly connections of epileptic patients in each group.
    Evaluate the compliance to the digital application by counting the number of connections

    Secondary Outcome Measures

    Feeling the frequency of lexical access problems
    Interview : Questionnaire language score : 0 to 12 points : 12 = worse outcome
    Self-esteem assessment
    Interview : Self-esteem score (Rosenberg scale) 0 to 40 points : 40 = better outcome
    Mood assessment
    Depression scale score (Neurological Disorder Depression Inventory for Epilepsy : NDDI-E) : 6 to 24 points : 24 = worse outcome
    Anxiety assessment
    Anxiety scale score : (Generalized Anxiety Disorder: GAD-7) : 0 to 21 points : 21 = worse outcome
    Information processing speed
    Computerized Speed Cognitive Test (CSCT): processing speed index: number of correct items in 90 sec. 0 to 110 points : 110 = better outcome
    Lexicon access assessment
    Lexicon access tests (Denomination Orale 80): number of correctly named words (0 to 80 words) : 80 = better outcome
    lexicon access assessment in time
    Lexicon access tests (Denomination Orale 80): time in second
    Selective and sustained attention assessment
    Selective Attention Test: Paced Auditory Serial Audition Test 4 seconds (PASAT): 0 to 60 score : 60 = better outcome
    Working memory assessment
    Backward digit span: number of digits recalled correctly in inverse order: 0 to 9 score: 9 = better outcome
    Verbal fluency assessment
    Verbal Initiation Test: Phonological Fluency: number of words beginning with P given in 2 minutes 0 to 50 words Category fluency test: number of words given in 2 minutes that belong to the category of Animals.0 to 50 words
    Naming assessment Boston naming task
    Number of correctly named words Boston Naming Test: number of correctly named words :0 to 50 points : 50 = better outcome
    Naming assessment in time
    Number of correctly named words Boston Naming Test: time in second
    Naming assessment BETL
    Number of correctly named words (BETL task : batterie evaluation troubles lexicaux = assessment of lexical impairment battery) 0 to 54 point : 54 = better outcome
    Naming assessment BETL intime
    BETL task : batterie evaluation troubles lexicaux = assessment of lexical impairment battery) : time in second

    Full Information

    First Posted
    June 29, 2021
    Last Updated
    September 15, 2021
    Sponsor
    Central Hospital, Nancy, France
    Collaborators
    UCB Pharma
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05057156
    Brief Title
    Digital Solution to Improve Cognitive Function in Epilepsy: PRODDIGE Project
    Acronym
    PRODDIGE
    Official Title
    Digital Solution to Improve Cognitive Function in Epilepsy: PRODDIGE Project
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2021
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    October 2021 (Anticipated)
    Primary Completion Date
    October 2023 (Anticipated)
    Study Completion Date
    March 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Central Hospital, Nancy, France
    Collaborators
    UCB Pharma

    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
    Background: Epilepsy leads to cognitive impairment in 20-50%. Compared to seizures, these cognitive disorders are a major additional factor in occupational, social and family disability. Memory and language skills are most often impaired. These disorders are well described, multifactorial, but no therapy (drug and/or non-drug) has been validated to date. Recently, cognitive remediation techniques have shown benefits in certain neurological pathologies, such as multiple sclerosis. In adult epilepsy, few previous cognitive remediation studies were performed but suffer significant methodological shortcomings that limit the scope of their results. Studies that have focused on cognitive function have shown promising results for attention and memory. In contrast, in the area of language, no studies have been published. Objective: to evaluate the effectiveness of a digital solution (PRODDIGE*) on the lexical access capacities in people with epilepsy. Method: Randomized, multicentric, observational study which will compare the use of a digital solution (PRODDIGE) in total autonomy versus the supervised use by a trained neuropsychologist. A neuropsychological assessment will be provided before and after a period of 4 months of use of the digital solution. Material: The medical project aims to offer an application of cognitive remediation to patients who suffer from cognitive impairments and especially language disorders. T The App is like a serious game, it's based on the playfulness of "game" and the seriousness of "medical exercise". During the exercise the patient can ask for clues help and isn't constrained by time in order to succeed "his mission". Conclusion: This will be the first French speaking app specifically dedicated to rehabilitation of language deficits observed in people with epilepsy. The expected benefits are an improvement of the patients' language complaints, the regular use of an adapted digital solution to improve their language difficulties, but also a better understanding of their disorders and an improvement of their self-esteem.
    Detailed Description
    o best help patients, Norsys enterprise designed the app with three key principles: Co-designed, to encourage the emergence of original solutions about uses from patients and therapists, User-friendly, to encourage the patient to exercise regularly and with pleasure (soft, optimistic, pleasant and calm mood), Accessible design, to get an application compatible and adapted to the specifics of these patients (contrast, color, typography, manipulation) According to these principles, the app gives access to 6 mini-games in its first version and will be available on iOS and Android smartphones. These exercises allow patients to work on specific aspects of their pathologies, this is how the exercises are intended to be playful, dynamic (ex. drag'n'drop) and sometimes collaborative.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cognitive Change

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    multicentric, transversal and randomized trial.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    90 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    "application supervised by a psychologist via teleconsultations"
    Arm Type
    Experimental
    Arm Description
    patient have app, and teleconsultation with psychologist
    Arm Title
    "application in total autonomy"
    Arm Type
    Placebo Comparator
    Arm Description
    patients have app, they play when they want
    Arm Title
    "control" group without using the application
    Arm Type
    No Intervention
    Arm Description
    patients haven't app
    Intervention Type
    Behavioral
    Intervention Name(s)
    cognitive rehabilitation
    Intervention Description
    patients have to use an app with cognitive games
    Primary Outcome Measure Information:
    Title
    Number of weekly connections of epileptic patients in each group.
    Description
    Evaluate the compliance to the digital application by counting the number of connections
    Time Frame
    5 months
    Secondary Outcome Measure Information:
    Title
    Feeling the frequency of lexical access problems
    Description
    Interview : Questionnaire language score : 0 to 12 points : 12 = worse outcome
    Time Frame
    0 and 5 months
    Title
    Self-esteem assessment
    Description
    Interview : Self-esteem score (Rosenberg scale) 0 to 40 points : 40 = better outcome
    Time Frame
    0 and 5 months
    Title
    Mood assessment
    Description
    Depression scale score (Neurological Disorder Depression Inventory for Epilepsy : NDDI-E) : 6 to 24 points : 24 = worse outcome
    Time Frame
    0 and 5 months
    Title
    Anxiety assessment
    Description
    Anxiety scale score : (Generalized Anxiety Disorder: GAD-7) : 0 to 21 points : 21 = worse outcome
    Time Frame
    0 and 5 months
    Title
    Information processing speed
    Description
    Computerized Speed Cognitive Test (CSCT): processing speed index: number of correct items in 90 sec. 0 to 110 points : 110 = better outcome
    Time Frame
    0 and 5 months
    Title
    Lexicon access assessment
    Description
    Lexicon access tests (Denomination Orale 80): number of correctly named words (0 to 80 words) : 80 = better outcome
    Time Frame
    0 and 5 months
    Title
    lexicon access assessment in time
    Description
    Lexicon access tests (Denomination Orale 80): time in second
    Time Frame
    0 and 5 months
    Title
    Selective and sustained attention assessment
    Description
    Selective Attention Test: Paced Auditory Serial Audition Test 4 seconds (PASAT): 0 to 60 score : 60 = better outcome
    Time Frame
    0 and 5 months
    Title
    Working memory assessment
    Description
    Backward digit span: number of digits recalled correctly in inverse order: 0 to 9 score: 9 = better outcome
    Time Frame
    0 and 5 months
    Title
    Verbal fluency assessment
    Description
    Verbal Initiation Test: Phonological Fluency: number of words beginning with P given in 2 minutes 0 to 50 words Category fluency test: number of words given in 2 minutes that belong to the category of Animals.0 to 50 words
    Time Frame
    0 and 5 months
    Title
    Naming assessment Boston naming task
    Description
    Number of correctly named words Boston Naming Test: number of correctly named words :0 to 50 points : 50 = better outcome
    Time Frame
    0 and 5 months
    Title
    Naming assessment in time
    Description
    Number of correctly named words Boston Naming Test: time in second
    Time Frame
    0 and 5 months
    Title
    Naming assessment BETL
    Description
    Number of correctly named words (BETL task : batterie evaluation troubles lexicaux = assessment of lexical impairment battery) 0 to 54 point : 54 = better outcome
    Time Frame
    0 and 5 months
    Title
    Naming assessment BETL intime
    Description
    BETL task : batterie evaluation troubles lexicaux = assessment of lexical impairment battery) : time in second
    Time Frame
    0 and 5 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Person with epilepsy, according to Fisher et al. (2005) criteria: all type of epilepsy could be include (new-onset and drug-resistant) Treatment must have been stable for 4 months: have the same molecule Person who has received full information about the organization of the research and has not objected to his or her participation and the use of his or her data Person aged 18 and over Mandatory affiliation to a social security scheme Validated cognitive inclusion criterion: having a YES response on the cognitive complaint questionnaire : A.Spontaneous complaint : Does the patient spontaneously complain of language difficulties? B.Subjective complaint : Do you search for your words? Do you sometimes feel like you have the word on the tip of your tongue? Do you sometimes have trouble finding the names of people you know well? Do you ever say one word for another? Exclusion Criteria: Person with another neurological condition Patients and normal control : A person over the age of majority who is subject to a legal protection measure or who is unable to express their consent. Person deprived of liberty by a judicial or administrative decision A person who regularly uses psychoactive substances (cannabis, alcohol, etc.).
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    helene brissart, PhD, HDR
    Phone
    3383851689
    Email
    h.brissart@chru-nancy.fr
    First Name & Middle Initial & Last Name or Official Title & Degree
    louis maillard, Pr
    Phone
    383852377
    Email
    l.maillard@chru-nancy.fr

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Digital Solution to Improve Cognitive Function in Epilepsy: PRODDIGE Project

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