Integrative Group-based Cognitive Rehabilitation Efficacy in Multiple
Integrative Group-based Cognitive Rehabilitation Efficacy in Multiple Sclerosis: a Randomized Clinical Trial
What it found
We found no results in the registry or in papers.
This trial finished 13 years ago. We found no results in the registry or in any paper that cites it.
What was tested
Treatment tested
- cognitive remediation program: REHACOP
What it measured
Main measures
Change in attention after receiving cognitive rehabilitation treatment
3 months
Thinking and memoryChange in working memory after receiving cognitive remediation treatment
3 months
Thinking and memoryChange in processing speed after receiving cognitive remediation treatment
3 months
Thinking and memoryChange in verbal memory after receiving cognitive remediation treatment
3 months
Thinking and memoryChange in verbal fluency after receiving cognitive remediation treatment
3 months
Thinking and memoryChange in executive functioning after receiving cognitive remediation treatment.
3 months
Thinking and memory
Who could take part
Relapsing and progressive · 20 to 60
Show the full criteria
Inclusion criteria
i) age 20-60 years ii) either male or female iii) patients with relapsing-remitting, secondary progressive or primary progressive MS
Exclusion criteria
i) presence of dementia ii) have suffered an exacerbation during the previous month to the cognitive assessment iii) being treated with corticosteroids iv) presence of other neurological disorder v) history of stroke or traumatic brain injury resulting in more than 30 minutes loss of consciousness vi) presence of psychiatric disorders
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
The study design was a parallel-group randomized trial with equal randomization. Recruitment and enrollment were conducted between January 2013 and March 2013. At base-line, cognitive data was collected. Afterwards, the participants were randomly allocated to either the REHACOP group or the Control group. During 3 months the intervention with REHACOP program took place and at follow-up patients were again re-evaluated to evaluate the change in cognitive measure. Post-treatment assessment (finished by July 2013) was performed within the first week after completing the intervention. Optional enrollment in pre-post neuroimaging will also allow us to look at changes in the brain. Objective: To examine the efficacy of an integrative cognitive training program (REHACOP) to improve cognition of patients with Multiple Sclerosis (MS).
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History
Started
Jan 2013
Main results due
Jul 2013
Finished
Jul 2013