Skip to main content
Clinical Trials/NCT04817124
NCT04817124
Completed
Not Applicable

Feasibility of Cognitive Training in Combination With Transcranial Direct Current Stimulation in a Home-based Context

University Medicine Greifswald1 site in 1 country30 target enrollmentMay 21, 2021
ConditionsAging

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aging
Sponsor
University Medicine Greifswald
Enrollment
30
Locations
1
Primary Endpoint
Feasibility of conducting the intervention in a home-based context
Status
Completed
Last Updated
last year

Overview

Brief Summary

The aim of this study is to investigate whether a tDCS-accompanied intensive cognitive training is feasible as a home-based intervention.

Detailed Description

The goal of the present study is to assess feasibility (primary) and cognitive training and transfer effects of a home-based multi-session cognitive training combined with transcranial direct current stimulation (tDCS). tDCS, particularly in combination with cognitive training, represents a promising approach to counteract cognitive decline and restore impaired functions. However, combined interventions of cognitive training and tDCS involve frequent visits to the facility, which leads to the need of space, time and personnel, and imposes strains on the participants. This study will elucidate the feasibility of tDCS and cognitive training in a home-based context. Healthy older adults will participate in a two-week cognitive training with concurrent online tDCS application in their own homes. Feasibility, as well as cognitive performance 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. A Follow-up session to assess long-term effects is planned four weeks after the post assessment. We hypothesize that with appropriate training of the participants and close supervision the use of combined tDCS and cognitive training in an ecologically valid environment by the participants themselves is feasible. In addition, we hypothesize this protocol will lead to improved performance on the trained tasks in both experimental groups. We expect increased performance on transfer tasks and long-term maintenance of the effects after anodal compared to sham stimulation. A successful implementation of the intervention in the home-based setting will contribute to the development of home-based tDCS as a widely available therapy option in clinical populations.

Registry
clinicaltrials.gov
Start Date
May 21, 2021
End Date
November 16, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Medicine Greifswald
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age: 60 - 80 years
  • Right handedness

Exclusion Criteria

  • Neurodegenerative neurological illnesses, epilepsy or history of seizures
  • Severe and untreated medical conditions that preclude 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 to tDCS application

Outcomes

Primary Outcomes

Feasibility of conducting the intervention in a home-based context

Time Frame: 2 weeks

Feasibility of home-based tDCS as operationalized by at least 2/3 (out of 6 planned sessions) successfully performed interventional sessions per participant. A session is regarded as successful if it is marked as completed in the stimulation system.

Secondary Outcomes

  • Working memory performance at follow-up assessment(4 weeks after intervention)
  • Working memory training performance (Letter Updating Task) at follow-up assessment(4 weeks after intervention)
  • Feasibility (questionnaire)(2 weeks)
  • Working memory performance at post-assessment(2 weeks)
  • Working memory training performance (Letter Updating Task) at post-assessment(2 weeks)

Study Sites (1)

Loading locations...

Similar Trials