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Need for speed: a pilot study on feasibility of cognitive rehabilitation for patients with progressive multiple sclerosis (MS)

Need for speed: a pilot study on feasibility of cognitive rehabilitation for patients with progressive multiple sclerosis (MS) - Cognitive rehabilitation in progressive MS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON46532
Enrollment
18
Registered
2018-06-29
Start date
2018-05-18
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

attention) cognitive problems problems in thinking abilities (such as memory

Interventions

A computer based speed of processing training, based on the method of retraining, will be provided for 5 weeks (2 times a week, 60 minutes per session) to the experimental group (intensity to be adj
Cognition
Information Processing Speed
Multiple Sclerosis
Rehabilitation

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1) at least 18 years of age 2) confirmed diagnosis of progressive MS 3) mentally competent to give informed consent 4) able to follow instructions and to respond autonomously to questionnaires 5) sufficient motor skills to perform the computer-based trainings

Exclusion criteria

Exclusion criteria: 1) individuals with impaired vision to such extent that they cannot distinguish the stimuli of the SPT intervention 2) individuals with (a history of) other major neurological disorders (e.g. stroke) 3) individuals with current major psychiatric disorders (e.g. bipolar disorder) 4) individuals with a history (or current situation) of extensive drug abuse 5) no changes in medication use (antidepressants and psycho-active drugs) are allowed for the last 4 weeks (stable treatment regime) 6) individuals that already recently participated in cognitive rehabilitation (within the last year) are excluded from participation

Design outcomes

Primary

MeasureTime frame
Change in cognitive performance and subjective well-being perceived on cognitive functioning, mood, fatigue, and quality of life before and after the interventions are the main outcome parameters.

Secondary

MeasureTime frame
Not applicable.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)