Frontopolar Cortex and Motivation in Healthy Older Adults
Causal Role of Frontopolar Cortex for Motivation in Healthy Older Adults: a Transcranial Direct Current Stimulation Study
1 other identifier
interventional
26
1 country
1
Brief Summary
Motivation represents a core aspect of goal-directed behavior as it determines how much effort individuals are willing to invest to reach their goals. While research on effort-based decision-making focuses mainly on effort preferences in younger adults, loss of motivation might be a key component of the apathetic tendencies frequently seen in older adults. However, an open question refers to which brain mechanisms underlie motivational processes in older adults. The investigators have recently shown that the frontopolar cortex plays a crucial in motivating the exertion of rewarded effort in younger adults. The goal of the current study is to determine whether frontopolar cortex plays a crucial role for motivation also in older adults and may thus be a promising target for improving the motivation deficits in healthy aging. Participants perform computer-based experimental tasks measuring the propensity to exert cognitive or physical effort for monetary rewards. During task performance, participants receive anodal or sham transcranial direct current stimulation (tDCS) over their frontopolar cortex. The study tests whether tDCS over frontopolar cortex allows modulating participants' motivation to engage in rewarded effort.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jan 2018
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 20, 2017
CompletedFirst Posted
Study publicly available on registry
June 23, 2017
CompletedStudy Start
First participant enrolled
January 16, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2020
CompletedApril 29, 2021
April 1, 2021
2.5 years
June 20, 2017
April 27, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
participants' decisions to exert cognitive or physical effort for monetary rewards
The project seeks to test the causal role of FPC in discounting of cognitive and physical effort in healthy older adults. For that purpose, participants perform a task on a computer which requires the participants to decide whether the participants are willing to exert cognitive or physical effort for a monetary reward. Participants perform this task both under anodal and under sham stimulation. It is tested whether anodal, relative to sham, stimulation increases participants' willingness to engage in rewarded cognitive or physical effort.
All participants perform this decision-making task in both experimental sessions (i.e., both the anodal and the sham stimulation session) for 20 min while receiving anodal or sham stimulation.
Study Arms (2)
anodal transcranial direct current stimulation
EXPERIMENTALanodal transcranial direct current stimulation (current strength: 1 mA, duration: 20 min) over the frontopolar cortex
sham transcranial direct current stimulation
SHAM COMPARATORsham transcranial direct current stimulation (current strength: 1 mA, duration: 0.5 min) over the frontopolar cortex
Interventions
Participants receive anodal or sham transcranial direct current stimulation while performing effort-based decision tasks.
Eligibility Criteria
You may qualify if:
- Age 65-80 years
- Informed consent as documented by signature
- Normal or corrected-to-normal vision
- Cognitive and language ability to understand study content and procedure
- Normal cognitive functioning (assessed by MMST)
- BDI-II score \< 20
You may not qualify if:
- Negative response to TMS/tDCS in past
- History of seizure
- History of stroke or heart attack
- History of head injury
- Psychiatric or neurological disorder
- Metal in body/head
- Implanted medical products like pacemaker, medical pumps, heart catheter
- Headache
- Tinnitus
- Currently taking medication affecting the central nervous system
- Insufficient sleep in preceding night
- Excessive consumption of alcohol within last 24 hours
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Zurich
Zurich, 8006, Switzerland
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Philippe N Tobler, Prof.
University of Zurich
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- The participants are blind to whether the participants receive anodal or sham stimulation in a session.
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 20, 2017
First Posted
June 23, 2017
Study Start
January 16, 2018
Primary Completion
June 30, 2020
Study Completion
June 30, 2020
Last Updated
April 29, 2021
Record last verified: 2021-04
Data Sharing
- IPD Sharing
- Will not share