TREAT-AHC: Validation of a Clinical Assessment Scale Specific to Alternating Hemiplegia

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06007521
Collaborator
(none)
20
1
12
1.7

Study Details

Study Description

Brief Summary

Alternating Hemiplegia of Childhood (AHC) is a very rare neurological disorder of genetic origin, combining paroxysmal episodes and neurodevelopmental impairment. The disease is generally sporadic, and its incidence has been estimated at 1 in 100,000 births, with around 500 cases published worldwide. The true prevalence of AHC may be underestimated due to a lack of understanding of the disease and a high degree of phenotypic heterogeneity.

It should be noted that, to date, it is difficult to assess the clinical characteristics of AHC patients in a homogeneous way. The lack of disease-specific clinical outcome measures therefore constitutes a critical node for advancing AHC research. In addition, recognition of the pattern of movement disorders and the ability to classify their severity are very important and useful for the clinician. Homogeneous disease assessment will help plan rehabilitative and pharmacological interventions, facilitate monitoring of treatment outcomes, and predict prognosis.

This is why an AHC assessment scale have been developed in collaboration with clinical teams from the IAHCRC consortium.

The scale has already been tested and validated on Italian and Spanish patients. The aim of this study is therefore to validate the use of this same scale on our French population of AHC patients. The hypothesis of the study is that the practical use of this scale specific to alternating hemiplegia is reproducible. To this end, all the items on the scale will be scored independently for each patient by 4 neuropediatricians with expertise in the disease, in order to observe the reproducibility of the results obtained with this scale. The scale will be used for twenty AHC patients of all ages.

Condition or Disease Intervention/Treatment Phase
  • Other: interview with neurologist

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Validation of a Clinical Assessment Scale Specific to Alternating Hemiplegia
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Oct 1, 2024
Anticipated Study Completion Date :
Oct 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Patients with alternating hemiplegia

Patients with alternating hemiplegia, from 0 to 99 years old

Other: interview with neurologist
interview with neurologist

Outcome Measures

Primary Outcome Measures

  1. Composite primary endpoint : - missing data from the scale <5 - mean scores compared between the 4 neurologists are close to the scale's mid-point, i.e. floor and ceiling effects are < 20%, and skewness statistics are between 21 and 11 [At inclusion]

    All statistical tests will be performed using SPSS version 24.0 statistical software, and P < 0.05 will be considered significant. Validation of the use of the scale based on the results obtained independently by the 4 expert neurologists using a composite primary endpoint consisting of three criteria: missing data from the scale <5 mean scores compared between the 4 neurologists are close to the scale's mid-point, i.e. floor and ceiling effects are < 20%, and skewness statistics are between 21 and 11.

Eligibility Criteria

Criteria

Ages Eligible for Study:
0 Years to 99 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patient with confirmed diagnosis of AHC, unrestricted age range 0-99 years

  • At least one parent and/or legal guardian who understands and speaks the national language

Adult patients :
  • Gathering of the non-opposition of the patient and/or his legal representative
Minor patients :
  • Collection of non-opposition from parents/guardians
Exclusion Criteria:
  • Patient's refusal to participate in the study

  • Patient under court protection, unable to give consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service d'Epileptologie Clinique, des Troubles du Sommeil et de Neurologie Fonctionnelle de l'Enfant Bron Rhone France 69500

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT06007521
Other Study ID Numbers:
  • 69HCL23_0804
First Posted:
Aug 23, 2023
Last Update Posted:
Aug 23, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hospices Civils de Lyon
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 23, 2023