NCT06107556

Brief Summary

The retrospective study investigates the part of responsibility of neuromuscular disorders associated with chronic hemiparesis in walking impairment.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Oct 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 19, 2023

Completed
Same day until next milestone

Study Start

First participant enrolled

October 19, 2023

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 19, 2023

Completed
11 days until next milestone

First Posted

Study publicly available on registry

October 30, 2023

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2024

Completed
Last Updated

October 30, 2023

Status Verified

October 1, 2023

Enrollment Period

Same day

First QC Date

October 19, 2023

Last Update Submit

October 24, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • Coefficient of antagonist activation

    The coefficient of antagonist activation of gastrocnemius medialis and soleus was calculated from EMG data by the ratio between the root mean square amplitude during antagonist effort and maximal agonist effort for the same muscle.

    1 year

Interventions

Gait analysisDIAGNOSTIC_TEST

3D gait analysis with electromyographic measurements

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Person with a history of stroke

You may qualify if:

  • Adult
  • Person who performed tridimensional gait analysis in laboratory
  • Person who had a stroke at least 6 months before the gait analysis

You may not qualify if:

  • Any other neurological pathology or gait disorders
  • Botulinum toxin injection in the last 3 months before the gait analysis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Laboratoire Analyse et Restauration du Mouvement

Créteil, France

Location

MeSH Terms

Conditions

StrokeMobility LimitationMuscle SpasticityParesis

Interventions

Gait Analysis

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsMuscular DiseasesMusculoskeletal DiseasesMuscle HypertoniaNeuromuscular ManifestationsNeurologic Manifestations

Intervention Hierarchy (Ancestors)

GaitPhysical ExaminationDiagnostic Techniques and ProceduresDiagnosisPhysical Functional PerformancePhysical FitnessHealthPopulation Characteristics

Study Officials

  • Emilie Hutin

    Hôpitaux Universitaires Henri Mondor

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Emilie Hutin, Ph.D.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Director

Study Record Dates

First Submitted

October 19, 2023

First Posted

October 30, 2023

Study Start

October 19, 2023

Primary Completion

October 19, 2023

Study Completion

June 30, 2024

Last Updated

October 30, 2023

Record last verified: 2023-10

Data Sharing

IPD Sharing
Will not share

Locations