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Volitional Dysfunction in Self-control Failures and Addictive Behaviors

Volitional Dysfunction in Self-control Failures and Addictive Behaviors

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04498988
Enrollment
338
Registered
2020-08-05
Start date
2014-12-01
Completion date
2024-06-30
Last updated
2024-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Addictive Behavior, Alcohol Use Disorder (AUD), Executive Dysfunction, Self-Control, Tobacco Use Disorder

Keywords

Cognitive control, Decision-making, Impulsivity, Risk-seeking

Brief summary

The aim of this project is to elucidate whether impairments of cognitive control, performance-monitoring, and value-based decision-making and dysfunctional interactions between underlying brain systems are mediating mechanisms and vulnerability factors for daily self-control failures and addictive disorders.

Detailed description

Failures of self-control during conflicts between long-term goals and immediate desires are a key characteristic of many harmful behaviors, including unhealthy eating habits, lack of exercise and problematic substance use, which often have adverse personal consequences and incur great societal costs. The project aims to elucidate neurocognitive mechanisms mediating deficient self-control, both in daily self-control failures and in substance use disorders and behavioral addictions, which are characterized by a loss of control despite awareness of adverse consequences. A prospective cohort study was launched using a multi-level approach that combines (i) a comprehensive clinical assessment, (ii) behavioral task batteries assessing cognitive control and decision-making functions, (iii) task-related and resting state fMRI, and (iv) Smartphone-based ecological momentary assessment of daily self-control failures. From a representative community sample, three groups of participants were recruited (each n = 100; age 20 - 26) with (a) symptoms of non-substance related and (b) substance-related addictive disorders and (c) syndrome-free controls. Participants are invited to yearly clinical follow-up assessments and further multi-level assessments 3 and 6 years after initial recruitment. Results obtained so far (until 06/2020) provide converging evidence that task performance as well as brain activity in monitoring, control, and valuation networks is reliably associated with the propensity to commit real-life self-control failures. Results support a process model, according to which deficient performance-monitoring leads to an insufficient recruitment of control networks, which attenuates the impact of long-term goals on neural value signals and increases the likelihood of self-control failures. In the final funding period (until 06/2024), the clinical follow-up period will be extended to 7 years. In addition, stress markers will be assessed as possible moderators of self-control. With the cross-lagged panel design it is expected to make a substantial contribution to the central unresolved question whether dysfunctions of cognitive control are causally involved in the development and trajectories of self-control failures and addictive behaviors, as well as to the disputed question of communalities and differences between different addictive disorders. Thereby, the project will to contribute to mechanism-based models of self-control impairments as a foundation for improved prevention and therapy.

Interventions

OTHERObservational study without interventions

Sponsors

German Research Foundation
CollaboratorOTHER
Technische Universität Dresden
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to 27 Years
Healthy volunteers
Yes

Inclusion criteria

(at baseline): 1. age 19-27 2. fulfill the criteria for one of three groups (SUD, ND, controls) 3. written informed consent

Exclusion criteria

(at baseline): 1. no written informed consent or limited ability to understand the questionnaires and tasks 2. disorders that might influence cognition or motor performance (e.g. craniocerebral injury) 3. magnetic resonance contraindications 4. current treatment for mental disorders 5. current use of psychotropic medication or substances 6. lifetime psychotic symptoms, bipolar disorder, or other SUD or ND not under study 7. major depression, somatoform, anxiety, obsessive compulsive, or eating disorders within the last 4 weeks

Design outcomes

Primary

MeasureTime frameDescription
Changes in real-life self-controlAt baseline and 3 and 6 years after baselineEveryday self-control was assessed using an Ecological Momentary Assessment (EMA) protocol adapted from Hofmann, Baumeister, Förster, and Vohs (2012). Self-control was defined as enactment of desires in conflict-laden situations.
Changes in quantity and frequency of addictive behaviorsAt baseline and 1, 2, 3, 4, 5, 6, 7 years after baselineChanges in quantity and frequency of addictive behaviours, which are combined into a quantity-frequency index.
Changes in cognitive control abilitiesAt baseline and 3 and 6 years after baselineThe Cognitive Control Task Battery of the Collaborative Research Center (CRC) 940 with nine executive function tasks (Stroop, AX continuous performance, color-shape, stop signal, letter memory, number-letter, go-nogo, 2-back, category switch) is used to derive a latent variable representing individual differences in general executive functioning (GEF). For the latent variable modelling error rates and reaction times from the tasks were combined, were appropriate, into inverse efficiency scores (IESs).
Changes in impulsive decision-makingAt baseline and 3 and 6 years after baselineThe Value-Based Decision-Making (VBDM) battery of the Collaborative Research Center (CRC) 940 including four decision-making tasks with a Bayesian adaptive algorithm was used to adaptively assess impulsive decision-making. For the delay and probability discounting tasks, a hyperbolic value function was used describing that the subjective values of delayed (or probabilistic) reward decline hyperbolically according to the discounting rate k. For the mixed gambles task, a simple linear function was used in which loss aversion (λ) is the relative weighting of losses to gains in the participant's. Individuals with higher impulsive decision-making are assumed to display higher k values in the delay discounting task, lower k values in probability discounting tasks, and lower λ values in the mixed gambles task.
Changes in neural correlates of response inhibitionAt baseline and 3 and 6 years after baselineBlood oxygenation level dependent (BOLD) responses in tasks measuring response inhibition (Go/Nogo, Stroop) using 3 Tesla functional magnetic resonance imaging (fMRI).
Changes in neural correlates of error monitoringAt baseline and 3 and 6 years after baselineBOLD responses in a task measuring error monitoring (Stroop) using 3 Tesla fMRI.
Changes in neural correlates of value-based decision-makingAt baseline and 3 and 6 years after baselineBOLD responses in a task measuring value-based decision-making using 3 Tesla fMRI.
Changes in structural brain characteristicsAt baseline and 3 and 6 years after baselineGray matter volume, cortical thickness and white matter properties in theoretically motivated regions of interest (e.g., right inferior frontal gyrus (rIFG), ventromedial prefrontal cortex (vmPFC), anterior cingulate cortex (ACC), anterior insula (aINS)) using 3 Tesla structural MRI.
Changes in addictive disorder severityAt baseline and 1, 2, 3, 4, 5, 6, 7 years after baselineChanges in number of fulfilled criteria according to the Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5)

Secondary

MeasureTime frameDescription
PersonalityAt baselineAs moderator variable we assessed the NEO Five Factor Inventory (NEO-FFI; outcomes are the sum scores).
Positive and negative affectAt baselineAs moderator variable we assessed the Positive and Negative Affect Schedule (PANAS; outcomes are the sum scores).
Changes in the action and state orientationAt baseline and 3 and 6 years after baselineAs moderator variable we assessed the Action-State Orientation Scale (ACS-90; outcomes are the sum scores).
Changes in impulsivityAt baseline and 3 and 6 years after baselineAs moderator variable we assessed the Barratt Impulsiveness Scale (BIS-11; outcome is the sum score).
Changes in self controlAt baseline and 3 and 6 years after baselineAs moderator variable we assessed the Brief Self-Control Scale (BSCS; outcome is the sum score).
Changes in chronic stressAt baseline and 3 and 6 years after baselineAs moderator variable we assessed the Trier Inventory for Chronic Stress (TICS; outcome is the sum score).
IntelligenceAt baselineAs control variable we assessed the intelligence quotient (IQ) using the Wechsler Intelligence Test for Adults (WIE).

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026