Evaluation of the Efficiency of a Cognitive Remedial Program (PROCOG-SEP) Designed for Multiple Sclerosis Patients. A Double Blind Randomized Multicenter Trial.

Status unknownNot a drug-phase studyMS (type not specified)NCT01659593

What it found

No results found

We found no results in the registry or in papers.

What was tested

Treatment tested

  • procog

Placebo

  • Placebo

What it measured

Main measures

  • cognitive function measured by SRT-List score

    0-9 months

    Thinking and memory

Other measures (1)

  • quality of life measured by MusiQol

    0 -9 months

    Quality of life (reported by participants)

Who could take part

MS (type not specified) · 18 to 60

Show the full criteria

Inclusion criteria

* 18 ≤Aged ≤ 60 at baseline * Must be able to understand and read french language * Must sign the informed consent form * Must be affiliate to French social security * multiple sclerosis confirmed by Mac Donald criteria * EDSS ≤ 6.0 at baseline * Duration of multiple sclerosis ≤ 30 years at baseline * mild cognitive disorder ( at least 2 cognitive tasks, at most 5 )

Exclusion criteria

* under legal protection * treatment by corticosteroids in the past 4 weeks * cognitive remedial program already done * neuropsychologic assessment in the past 2 months * having an other chronic disease * having an other neurologic disease * alcohol or drug addiction

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

Cognitive disorders are well-known in multiple sclerosis (MS), even in earlier stages of the disease. They effect personal life. Their management may be overlooked. The evidence-based program proposes exercises to both stimulate preserved functions and develop new abilities compensating for cognitive disabilities. Aim of the study is to evaluate the efficiency of the remedial program (PROCOG-SEP) designed for MS patients, compared to an interactive discussion program(DISINT) 140 multiple sclerosis patients will be randomly assigned in one the program for 13 sessions over a 6-month period. Main outcome criteria is evolution of SRT-LIST before and after program.

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History

    1. Started

      Sept 2012

    2. Main results due

      Sept 2016

    3. Finished

      Jun 2018

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