ClinicalTrials.Veeva

Menu

Peer Support Impact on Therapeutic Adherence in Patients With Multiple Sclerosis (PAIR-SEP)

N

Nantes University Hospital (NUH)

Status

Not yet enrolling

Conditions

Multiple Sclerosis, Relapsing-remitting

Treatments

Other: Peer support

Study type

Interventional

Funder types

Other

Identifiers

NCT05519553
RC22_0175

Details and patient eligibility

About

A mixed methods randomized controlled trial pilot study to assess peer support impact on relapsing-remitting multiple sclerosis patients' therapeutic adherence.

Full description

Multiple sclerosis (MS) is a debilitating and incurable chronic disease. Patients might benefit from peer support provided by patients entitled to give advice on daily life management with MS. Studies have shown that peer support can enhance chronic patients' quality of life in Psychiatry and Oncology.

This pilot study aims at assessing the impact of peer support on therapeutic adherence and quality of life in patients with MS, but also to appraise the project feasibility and acceptability among the healthcare team, with large-scale implementation in mind.

This mixed methods pilot study consists in a monocentric open-label randomized controlled trial. It is located in Nantes, France, and aims to recruit 60 patients with relapsing-remitting MS undergoing drug therapy from the Nantes University Hospital Neurology Department. Patients will be randomized 1:1 to receive either usual care only or usual care combined with peer support (3 individual sessions at 1, 3 and 5 months with a peer support specialist).

Primary outcome is enhanced therapeutic adherence 6 months after baseline, secondary outcomes include therapeutic compliance, quality of life, anxiety and depression, social support. All dimensions will be assessed using validated health questionnaires at baseline and at 6 months.

Interventions acceptability and feasibility will be evaluated using qualitative methods: undirected interviews with patients from the intervention group and 2 focus-groups, one with the peer support specialists and the other with the healthcare team.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients
  • With relapsing-remitting MS according to 2017 revised Mc Donald criteria
  • Attending medical consultation at Nantes University Hospital Neurology Department
  • For whom background drug therapy is needed (oral or injectable)
  • Who gave consent to participate in trial

Exclusion criteria

  • Primary-progressive or secondary-progressive MS patients
  • Patients under protection of vulnerable adults measure or convicted
  • Patients not fluent in French
  • Patients with severe cognitive impairment, who may find difficult filling out questionnaires properly
  • Patients with a risk of follow-up interruption (move, nomadism...)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Experimental group
Experimental group
Description:
30 MS (Multiple sclerosis, relapsing-remitting) patients
Treatment:
Other: Peer support
Control group
No Intervention group
Description:
30 MS (Multiple sclerosis, relapsing-remitting) patients

Trial contacts and locations

0

Loading...

Central trial contact

Lebeaupin Maxime; Leïla MORET, MD - PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems