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AgingSoCoStimNCT04633499

Effects of tDCS on Social Cognition in Aging

A study testing Social Cognition Task and tDCS in people with Aging and Social Cognition, run by University Medicine Greifswald at 1 site in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of the study is to explore the effect of transcranial direct current stimulation (tDCS) on either the right tempo-parietal junction (rTPJ) or the dorsomedial prefrontal cortex (dmPFC) in healthy older adults (replication in a different sample of a study by Martin et al., 2020). Read more about this study

Who is it for?
Ages 18 to 80 yearsHealthy volunteers can take part
Conditions the study is for
Aging, Social Cognition
What is being tested?
Social Cognition Task and tDCS
Could I receive a placebo?
No, everyone receives an active treatment
How many people
90 participants
Where
1 siteGermany
Study dates
1 Aug 2020to 31 May 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • healthy older (60 - 80 years) and younger (18 - 30 years) participants
  • German as their main language or sufficient german skills to understand the experiment and the task

Who cannot join

  • participants with neuropsychological or psychiatric disease that affect cognition.
  • standard MRI exclusion criteria (e.g. pregnancy, metal implants)
  • standard tDCS exclusion criteria (e.g. metal implants in the head)

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • University Medicine Greifswald

    Greifswald, 17489

Other trials in Germany

About this study

Official title: Effects of tDCS on Visual Perspective Taking and Emotion Recognition in Healthy Older Adults

The aim of the study is to explore the effect of transcranial direct current stimulation (tDCS) on either the right tempo-parietal junction (rTPJ) or the dorsomedial prefrontal cortex (dmPFC) in healthy older adults (replication in a different sample of a study by Martin et al., 2020).

Read the detailed description

Humans are fundamentally social animals. The ability to operate within large social networks requires considerable cognitive capacity, often referred to as social cognition. One social cognitive process thought to involve embodied and nonembodied processes is perspective-taking. Recently, the right temporoparietal junction (rTPJ) has been suggested as a key hub for embodied processing relevant to social cognition. A study of Martin et al. (2020) could further provide causal evidence that the right temporoparietal junction is involved specifically in the embodied component of perspective-taking. Specifically, HD-tDCS (high-definition transcranial direct current stimulation) to the right temporoparietal junction, but not another hub of the social brain (dorsomedial PFC), increased the effect of body position during perspective-taking, but not tracking. As social cognition is affected by the aging process and decline of socio-cognitive abilities is a key feature of neurological diseases such as Alzheimer's or Parkinson's disease, the aim of the present study is to replicate the findings of Martin et al., (2020) in a sample of healthy older adults to better understand the modulation of socio-cognitive processes in older age.

The aim of the study is to explore the effect of transcranial direct current stimulation (tDCS) on either the right tempo-parietal junction (rTPJ) or the dorsomedial prefrontal cortex (dmPFC) in healthy older adults (replication in a different sample of a study by Martin et al., 2020). 60 healthy older adults and 30 younger participants (serving as a control group) will be tested in a Reading the Eyes in the Mind Task (RMET) and a Task of Visual Perspective Taking (VPT) , while stimulation either the rTPJ or the dmPFC with either active or sham tDCS (stimulation only in the group of older participants). In the RMET the expectation is that older participants have higher reaction times after correct answers under rTPJ tDCS. No stimulation effects of the dmPFC are expected. In the VPT older participants are expected to have a selective effect on body position (similar to the results of Martin et al., 2020) under rTPJ stimulation, but not dmPFC stimulation.

A further focus of the study is how functional and structural connectivity of the brain and individual differences measured with an MRI assessment influence with the success of the RMET and VPT paradigms in an explorative research question.

Being tested
Social Cognition Task, tDCS
Keywords
tDCS, Social Cognition

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Social Cognition TaskBehavioural

    Two paradigms will be tested: visual perspective taking and reading the mind in the eyes.

  • tDCSDevice

    tDCS either over the dmPFC or the rTPJ.

Study groups in NCT04633499
Study groupRoleWhat they receive
dmPFC tDCS + Social Cognition tasks in older participantsActive comparatorParticipants will receive either active or sham stimulation over the dmPFC while conducting two different social cognition paradigms: one regarding emotion recognition, one on visual perspective taking.
Receives: Behavioral: Social Cognition Task; Device: tDCS
rTPJ tDCS + Social Cognition tasks in older participantsExperimentalParticipants will receive either active or sham stimulation over the rTPJ while conducting two different social cognition paradigms: one regarding emotion recognition, one on visual perspective taking.
Receives: Behavioral: Social Cognition Task; Device: tDCS
Social cognition tasks in younger participantsActive comparatorParticipants will conduct two different social cognition paradigms: one regarding emotion recognition, one on visual perspective taking but without tDCS stimulation.
Receives: Behavioral: Social Cognition Task

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Response Time in milliseconds in Visual-Perspective Taking Paradigm (VPT) in the active tDCS.

    The outcome in the VPT paradigm will be response time in milliseconds (for correct answers only).

    Measured: at Day 1 or 7 (depends on randomization)

  2. Response Time in milliseconds in Visual-Perspective Taking Paradigm (VPT) in the sham tDCS.

    The outcome in the VPT paradigm will be response time in milliseconds (for correct answers only).

    Measured: at Day 1 or 7 (depends on randomization)

  3. Response Time in milliseconds in the Reading the mind in the eyes test (RMET) in the active tDCS.

    Outcome in the RMET will be reaction times in milliseconds (of correct answers only) in either rTPJ or dmPFC stimulation in comparison to sham stimulation.

    Measured: at Day 1 or 7 (depends on randomization)

  4. Response Time in milliseconds in the Reading the mind in the eyes test (RMET) in the sham tDCS.

    Outcome in the RMET will be reaction times in milliseconds (of correct answers only) in either rTPJ or dmPFC stimulation in comparison to sham stimulation.

    Measured: at Day 1 or 7 (depends on randomization)

Secondary outcomes (1)
  1. Functional and structural connectivity (via MRI)

    It will be investigated how functional and structural connectivity of the brain and individual differences measured with an MRI assessment influence with the success of the RMET and VPT paradigms in an explorative research question.Structural and functional connectivity will be assessed.

    Measured: MRI Assessment takes places before participants are stimulated with tDCS at Baseline (Day 1).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Nov 2020
  2. Study start1 Aug 2020
  3. Primary completion31 May 2022
  4. Study completion31 May 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
It is a randomized, balanced cross-over design with within- as well as between group comparisons. Two groups will be investigate: young participants (n = 30) and older participants (n = 60). The group of young participants will serve as a control group and will only get a neuropsychological assessment of their cognitive abilities at the beginning of the study, an MRI assessment and one session of the investigated paradigms (without tDCS). The group of older participants will conduct a session of MRI assessment and neuropsychological assessment, as well as two tDCS sessions (anodal/sham). The stimulation will either be over the rTPJ or the dmPFC. This set-up is identical to the study of Martin et al., (2020).
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
90 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04633499
Sponsor's protocol ID
SoCoStim
Acronym
SoCoStim
Status last verified
Jun 2022
First submitted
27 Aug 2020
Last updated
2 Jun 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Martin AK, Kessler K, Cooke S, Huang J, Meinzer M. The Right Temporoparietal Junction Is Causally Associated with Embodied Perspective-taking. J Neurosci. 2020 Apr 8;40(15):3089-3095. doi: 10.1523/JNEUROSCI.2637-19.2020. Epub 2020 Mar 4.

    PubMed 32132264
  • Roheger M, Mader A, Riemann S, Niemann F, Kessler K, Martin AK, Meinzer M. Intact embodiment during perspective-taking in older adults is not affected by focal tDCS. Geroscience. 2025 Dec;47(6):6823-6837. doi: 10.1007/s11357-025-01554-4. Epub 2025 Feb 19.

    PubMed 39966250

Questions about this trial

What is this clinical trial studying?

A study testing Social Cognition Task and tDCS in people with Aging and Social Cognition, run by University Medicine Greifswald at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Response Time in milliseconds in Visual-Perspective Taking Paradigm (VPT) in the active tDCS. (time frame: at Day 1 or 7 (depends on randomization)). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04633499, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jun 2022.

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