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Brain Stimulation and Cognitive Training in Healthy Older Adults (TrainStim)

U

University Medicine Greifswald

Status

Completed

Conditions

Aging

Treatments

Behavioral: Intensive cognitive training
Device: Anodal tDCS

Study type

Interventional

Funder types

Other

Identifiers

NCT03838211
TrainStim3

Details and patient eligibility

About

The aim of this study is to investigate whether a tDCS-accompanied intensive cognitive training of working memory leads to performance improvement in healthy older individuals.

Full description

The goal of the present study is to assess behavioral (primary) and neural effects of a multi-session cognitive training combined with transcranial direct current stimulation (tDCS). Many studies to date have found tDCS to be an efficient method to enhance various cognitive functions by modulating cortical excitability in young adults, but its behavioral impact and underlying mechanisms in aging still need to be elucidated. Healthy older adults will participate in a three-week cognitive training with concurrent online tDCS application. Cognitive performance (primary), as well as structural and functional imaging data will be examined before, during and after the intervention. In order to draw conclusions about the effect of tDCS in addition to cognitive training, a control group, receiving sham stimulation during training, will be assessed. Furthermore, to assess neural correlates of performance improvement, functional and structural parameters will be measured with MRI before and after training. Follow-up sessions to assess long-term effects are planned four weeks and six months after the post assessment. The results of the study will offer valuable insights into efficacy of combined tDCS and cognitive training, as compared to training alone, in older adults. Moreover, improved understanding of tDCS effects on cognitive training performance and underlying neural correlates may help to develop novel approaches for cognitive decline in healthy and pathological aging.

Enrollment

56 patients

Sex

All

Ages

65 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Older adults (65 - 80 years);
  • Right handedness;
  • Unobtrusive neuropsychological screening

Exclusion criteria

  • Mild cognitive impairment (MCI) or dementia; other neurodegenerative neurological disorders; epilepsy; previous stroke;
  • Severe and untreated medical conditions that precludes participation in the training, as determined by responsible physician;
  • History of severe alcoholism or use of drugs;
  • Severe psychiatric disorders such as depression (if not in remission) or psychosis;
  • Contraindication for MRI (claustrophobia, metallic implants, ferromagnetic metals in the body, disorders of thermoregulation, pregnant women)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

56 participants in 2 patient groups

stimulation group
Experimental group
Description:
Anodal tDCS + intensive cognitive Training
Treatment:
Behavioral: Intensive cognitive training
Device: Anodal tDCS
sham group
Sham Comparator group
Description:
Sham tDCS + intensive cognitive Training
Treatment:
Behavioral: Intensive cognitive training

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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