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Study of the Test-retest Reliability of the Neuropsychiatric Fluctuations Scale in Parkinson's Disease (EFN-RETEST)

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status

Not yet enrolling

Conditions

Parkinson's Disease

Treatments

Other: Questionnaire and Physical Exam

Study type

Interventional

Funder types

Other

Identifiers

NCT06701955
2024-A01403-44 (Other Identifier)
38RC24.0196

Details and patient eligibility

About

This study focuses on neuropsychiatric fluctuations (NPF) in Parkinson's disease. Due to the lack of specific assessment tools, we developed the Neuropsychological Fluctuations Scale (NFS), a 20-item questionnaire. Recent studies have confirmed its reliability, sensitivity, and validity. To finalize its validation, assessing its test-retest reliability is an essential next step.

Full description

During the progression of Parkinson's disease, a large number of patients experience fluctuations in motor status associated with neuropsychiatric fluctuations (NPF) (alternating episodes of depression, anxiety, and apathy with hypomanic states, impulsivity, and attention disorders). NPF may have a significant impact on patients' quality of life as well as on that of their caregivers. Moreover, the presence of these fluctuations is a risk factor for the development of self-medication behaviors, which can lead to addiction to antiparkinsonian treatments.

Due to the lack of specific tools for assessing NPF, our team developed a 20-item self-questionnaire specifically evaluating NPF in acute phases: the Neuropsychological Fluctuations Scale (NFS), which was first published in Movement Disorders, Clinical Practice (Schmitt et al., 2018). Recently, we studied the psychometric properties of the NFS in two populations of Parkinson's disease patients and in the general population (EFN Pre-Validation and EFN-Validation studies: ClinicalTrials.gov NCT04455074). The results regarding internal consistency, sensitivity, and specificity of the NFS, as well as its internal structure and external validity, were published in Frontiers in Neurology in 2023 (Schmitt et al., 2023). It has been demonstrated that the NFS is an innovative tool that complements existing motor and non-motor evaluations, and its utility in diagnosing and managing NPF is significant.

In order to finalize the validation of the NFS and further understand its psychometric characteristics, assessing the temporal stability of the NFS through test-retest reliability is an essential step.

Enrollment

100 estimated patients

Sex

All

Ages

30 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age > 30 and ≤ 75 years

  • Idiopathic Parkinson's disease (according to the criteria of the Movement Disorders Society)
  • Presence of motor fluctuations described by the patient, their relatives, or identified by the clinician
  • Stability of antiparkinsonian treatment for at least one month
  • Mastery of the French language
  • Able to give consent.
  • Affiliated to the social security system

Exclusion criteria

Parkinsonian syndrome other than idiopathic Parkinson's disease

  • Dementia (MoCa < 23)
  • No antiparkinsonian treatment or treatment modified for less than one month
  • Persons referred to in Articles L1121-5 to L1121-8 of the CSP (corresponds to all protected persons: pregnant women, parturients, breastfeeding mothers, persons deprived of liberty by judicial or administrative decision, persons receiving psychiatric care under Articles L. 3212-1 and L. 3213-1 who are not covered by the provisions of Article L. 1121-8, persons admitted to a health or social establishment for purposes other than research, minors, persons subject to a legal protection measure or unable to express their consent))
  • Subject in a period of exclusion from another interventional study.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

sequence of intervention
Other group
Description:
self administered questionnaires at different time points..
Treatment:
Other: Questionnaire and Physical Exam

Trial contacts and locations

1

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Central trial contact

Andrea Kistner; Emmanuelle Schmitt, PHD

Data sourced from clinicaltrials.gov

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