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Implementation Intention for Physical Activity in Multiple Sclerosis (apsep)

U

University of Paris 5 - Rene Descartes

Status

Unknown

Conditions

Motivation
Mindfulness

Treatments

Behavioral: Motivation

Study type

Interventional

Funder types

Other

Identifiers

NCT03785483
apsep-01

Details and patient eligibility

About

The purpose of this study is to evaluate the effectiveness of an 8-week intervention based on implementation intention (motivation) in patients with multiple sclerosis on objectively measured physical activity.

Enrollment

45 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult aged between 18 and 65 years
  • Multiple sclerosis
  • Recruited from CHU Poissy saint germain or Hôpital Raymond-Poincaré
  • Informed consent provided during inclusion interview

Exclusion criteria

  • Already participating in a clinical trial
  • Cognitive dysfunctions in understanding simple guidelines
  • Treatment reducing fatigue since less than 3 months
  • Psychiatric disorders
  • Unability to exercise
  • Previous cardiovascular diseases
  • Regular physical activity practice

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

45 participants in 3 patient groups

Motivation
Experimental group
Description:
Using implementation intention techniques such as action planning. Every week, participants state when, where, and what kind of prescribed exercises they will do.
Treatment:
Behavioral: Motivation
Mindfulness
Active Comparator group
Description:
10 minutes of audio recordings daily. Recordings contain: awareness of the breath, acceptation of thoughts and emotions, awareness of postures, awareness during stretching, awareness of a single movement (moving legs up while standing).
Treatment:
Behavioral: Motivation
Treatment as usual
No Intervention group
Description:
Physical activity prescribe 120 minutes per week.

Trial contacts and locations

2

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Central trial contact

Giovanni De Marco, Pr; Jean F Fournier, PhD

Data sourced from clinicaltrials.gov

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