Skip to content

Sensory-cognitive and Physical Fitness Training in Mild Cognitive Impairment

Computer-based Sensory-cognitive and Physical Fitness Training in Mild Cognitive Impairment (MCI) and Mild Alzheimer's Disease (AD)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01061489
Enrollment
65
Registered
2010-02-03
Start date
2009-08-31
Completion date
2013-03-31
Last updated
2016-07-14

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

Conditions

Mild Alzheimer's Disease, Mild Cognitive Impairment (MCI)

Keywords

neuroplasticity, Mild Cognitive Impairment (MCI), Alzheimer, sensory-cognitive training, physical fitness

Brief summary

Age-related cognitive decline is unavoidable. However, recent results of neuroplasticity-based research show that neuroplasticity-based training and physical activity might have the potential to decelerate or even reverse effects of aging and age-related cognitive impairments. Little is known whether these results also apply to pathological processes of aging such as mild cognitive impairment (MCI) and dementia. This multi-center study aims at investigating efficiency and feasibility of a neuroplasticity-based auditory discrimination training and a physical fitness training for patients suffering from mild cognitive impairment or mild Alzheimer's disease (Mini Mental State Examination, MMSE \> 19). Evaluation will include neuropsychological testing, electroencephalography (EEG) and magnetic resonance imaging (MRI) measurements as well as blood and liquor analyses.

Interventions

OTHERauditory discrimination training

10-week neuroplasticity-based training (5 days/week, 1 hour each, PC-based), training at home

OTHERphysical movement training

10-week training, small groups (2 days/week, 1 hour each) plus homework (3 days/week)

Sponsors

University of Ulm
CollaboratorOTHER
University of Konstanz
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* focus: subjective and/or objective memory complaints with MMSE \> 19 (MCI or mild Alzheimer's Disease, with stable medication for at least 3 months) * mild to moderate depression * corrected-to-normal hearing and vision * for MRI: non-magnetic metals inside the body * right handedness preferred

Exclusion criteria

* cognitive impairment/ dementia with MMSE \< 20, severe psychiatric or neurological disease (current and lifetime) * physical health that does not allow physical fitness tests and trainings * benzodiazepin, tricyclic antidepressants * for MRI: magnetic metal inside the body, cardiac pacemaker etc. * for liquor: insufficient blood coagulation, insufficient brain pressure

Design outcomes

Primary

MeasureTime frameDescription
Change in global cognitionpre, post, 3-month follow-upAverage score of the two component scores memory and attention / executive functions, derived from principal component analysis of 11 cognitive items (Munich verbal memory test (MVGT) encoding, MVGT long delayed free recall, free recall of the Alzheimer's Disease Assessment Scale, working memory in the Everyday Cognition Battery, Trail Making Test A and B, digit span forward and backward, digit-symbol-coding and semantic and phonematic fluency).

Secondary

MeasureTime frame
electrophysiological, MRI, blood and liquor correlatespre, post, 3-month follow-up

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026