Ireland
--:--IST
Starting soon Observational

Feasibility Study of a Relapse Investigation Questionnaire Administered by an MS Care Coordinator Nurse in Patients With Multiple Sclerosis

NCT06994026 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-06-15
Last updated
2025-05-29

Condition(s) studied

Multiple SclerosisDisease ManagementFeasibility Studies

Study summary

This study aims to evaluate a questionnaire used by a specialized nurse to help manage relapses in people with multiple sclerosis (MS). The questionnaire is completed during a phone call when the patient reports new or worsening symptoms. It helps the nurse decide whether further tests or treatments are needed, based on a protocol developed with a neurologist. The goal is to improve how quickly and effectively patients receive care during a relapse. The study will include 10 adult patients with active forms of MS over a two-month period.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients followed by Dr. Manchon for Relapsing-Remitting Multiple Sclerosis or active Secondary Progressive Multiple Sclerosis * Adult patients (aged 18 or older) * Patients who have provided informed consent for participation in the local task-sharing protocol Exclusion Criteria: * Pregnant women * Minors (under 18 years old) * Patients with known renal failure * Patients who have not provided or are unable to provide consent for the local task-sharing protocol

Primary outcome measure(s)

  • Effectiveness of the relapse investigation questionnaire completed by the MS care coordinator nurse (IDEC) in guiding the patient's care pathway during a suspected relapse, according to the local task-sharing protocol. — June 2025 - August 2025

Trial sites (1)

FacilityCityRegionStatus
France Gonesse France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06994026 on ClinicalTrials.gov ↗ ← All trials in France