The Effect of Aging on Value Based Decision-making

May 20, 2019 updated by: Isabelle Brocas, University of Southern California

A Neuroeconomic Study of Choice Consistency in Aging

The investigators propose to study the effect of aging on the neural circuitry involved in valuation and value reasoning and to relate it to choice anomalies and inconsistencies. Quantifying and characterizing valuation-based decision-making deficits in older adults, and their relationship to the aging brain, can inform and facilitate intervention - both at the level of the individual and at the level of policy.

Study Overview

Status

Completed

Conditions

Detailed Description

The attribution of value to prospects is a fundamental element of decision-making, as most day-to-day decisions involve comparing items. Studies on aging document behaviors reflecting difficulties in making comparisons between options, in particular when those options are complex. Given the growing complexity of economic products (insurance, savings, mortgages or even telephone plans), older adults may have difficulty making decisions that accurately reflect their underlying preferences. It is plausible that this difficulty is linked to age-related brain function decline within sectors of the lateral prefrontal cortex implicated in working memory and cognitive control. This study assesses age-related changes in how the brain computes value and makes value comparisons using a well-established economic paradigm, the "generalized axiom of revealed preference" (GARP) Task, that tests the internal consistency of a subject's preferences by offering repeated choices between bundles of goods. A preliminary study suggests that aging is associated with greater GARP-Task inconsistency. Although the neural correlates of GARP inconsistency have not been directly established, indirect evidence suggests that the medial orbitofrontal cortex is important in all value-based decision-making, and that areas in the lateral prefrontal and parietal cortices (fronto-parietal network) are important for maintaining consistency in complex decisions (e.g., multi-attribute decisions). Aging is associated with structural and functional deficits within the fronto-parietal network. Therefore, the investigators believe that studying the neural correlates of the GARP-Task is a promising approach to investigate decision-making deficits in aging. The investigators will recruit 45 young adults, and 45 old adults. Participants will complete the GARP-Task and an functional Magnetic resonance imaging (fMRI) variant designed to isolate neural correlates of valuation of single items, of multiple instances of the same item ("scaling") and of sets of distinct items ("bundles"). Brain activity will be related to diagnosis and to variance in GARP-Task inconsistency. Given the prominence of age-related decline in working memory, the investigators hypothesize that age will be associated with higher GARP-Task inconsistency and to deficits in conditions that require manipulation of value signals (scaling and bundles). The investigators anticipate that these deficits will be associated with low recruitment within the fronto-parietal network and with reduced functional connectivity between this network and the medial Orbitofrontal Cortex (OFC).

Study Type

Observational

Enrollment (Actual)

90

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Los Angeles, California, United States, 90089
        • LABEL

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Healthy adults above 18yo

Description

Inclusion Criteria:

  • Healthy adults

Exclusion Criteria:

  • 1- Subjects under 18yo . 2- Subjects with known cognitive disorders 3- Subjects with visual or auditory deficits that would interfere with the ability to complete the experimental tasks.

    4- Subjects reporting having metal implants 5- Subjects with a history of major anxiety disorder or other major psychiatric condition, 6- Subjects with a documented or subjectively reported claustrophobia. 7- Subjects thinking they are or may be pregnant. 8- Subjects with a history of head trauma that resulted in loss of consciousness for more than 5 minutes.

    9-Hx of seizures 10-Left Handed 11- On any medications affecting cognition 12- For tasks involving foods: a) Currently on diet and or b) any known food allergies

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Adults 55 and younger
All participants will make simple decisions while in a scanner.
Adults 55 and older
All participants will make simple decisions while in a scanner.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Computerized behavioral choice task
Time Frame: 2 hours
The task consists in 450 trials. In each trial, the participant needs to choose between food items presented on a computer screen. Frequency of choices is used to assess the ranking (or value) of these food items and inconsistencies in choices are recorded. Food items vary in complexity (from single items to complex bundles).
2 hours
Brain imaging to track brain regions involving in value
Time Frame: 1 hour
fMRI images are collected during part of the behavioral choice task. Behavioral measures are used to track value encoding as well as inconsistent choices in the brain (as a function of item complexity). These data are eventually aggregated across participants in each condition (using standard methods) to identify the regions of interest involved in our experiment.
1 hour

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Isabelle Brocas, PhD, University of Southern California

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2016

Primary Completion (Actual)

April 30, 2018

Study Completion (Actual)

April 30, 2018

Study Registration Dates

First Submitted

November 6, 2017

First Submitted That Met QC Criteria

November 8, 2017

First Posted (Actual)

November 14, 2017

Study Record Updates

Last Update Posted (Actual)

May 22, 2019

Last Update Submitted That Met QC Criteria

May 20, 2019

Last Verified

May 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 1R21AG046917-01A1 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

We will share all data and results.

IPD Sharing Time Frame

After publication

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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