Social Feedback and Dysfunctional Risk Taking in NSSI Adolescents

Sponsor
University of Electronic Science and Technology of China (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05981677
Collaborator
(none)
80
47

Study Details

Study Description

Brief Summary

Nonsuicidal self-injury (NSSI) is defined as direct, intentional physical injury without suicidal intention. Problematic interpersonal relationships and decision-making have been demonstrated to play crucial roles in this maladaptive behavior, especially for adolescents. Accumulating evidence suggests that decision processes and risk-taking are strongly influenced by the affective state of the individual. However, whether these interactions are disrupted in NSSI adolescents has not been systematically examined. In the current study, the investigators modified one of the most widely used paradigms for measuring an individual's risk decision-making, the Balloon Analogue Risk Task (BART). The investigators combine social reward (green balloon), punishment (red balloon), and control feedback (yellow balloon), to investigate whether the NSSI adolescents have dysfunctional risk-taking behavior while facing different social outcomes. The investigators recruit one group of NSSI adolescents (n = 40) and one health control (HC) group (n = 40), to compare their risk-related decisions during the emotional BART. The investigators hypothesize that compared to HC, NSSI adolescents will show altered effects of social reward and punishment on risk-related decision-making, in particular higher risk avoidance in the context of social punishment.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    80 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Cross-Sectional
    Official Title:
    Risk and Social Feedback in Adolescents With Nonsuicidal Self-Injury
    Anticipated Study Start Date :
    Aug 1, 2023
    Anticipated Primary Completion Date :
    Jul 1, 2026
    Anticipated Study Completion Date :
    Jul 1, 2027

    Arms and Interventions

    Arm Intervention/Treatment
    NSSI

    HC

    Outcome Measures

    Primary Outcome Measures

    1. Risky avoidance measured by BART [About 20 minutes]

      Adjusted number of pumps (average number of pumps excluding balloons that exploded) as the index of risk avoidance. Alterations in the patients will be determined by using ANOVA models with the group (NSSI vs. HC) as a between-subject factor and emotional feedback (social reward, social punishment, and control) as a within-subject factor.

    2. Decision-making measured by BART [About 20 minutes]

      Earned money (total amount of money earned in the task) as the index of decision-making. Alterations in the patients will be determined by using ANOVA models with the group (NSSI vs. HC) as a between-subject factor and emotional feedback (social reward, social punishment, and control) as a within-subject factor.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    15 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 15-18 years

    • right-handed

    • normal or corrected normal visual acuity

    • meet the proposed DSM-5 frequency criteria (e.g., ≥5 days of NSSI behaviors in the past year)

    Exclusion Criteria:
    • diagnosis of borderline personality disorder, major depressive disorder, other

    • psychiatric disorders, etc.

    • high suicidal risk

    • recent use of medications that can affect neural activity

    • have received or are receiving Dialectical Behavior Therapy (DBT) other treatment for emotional problems within the past 6 months

    • have a contraindication to MRI scanning (e.g., metal implants, claustrophobia or other conditions that make them inappropriate for MRI scanning)

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Electronic Science and Technology of China

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Benjamin Becker, Professor, University of Electronic Science and Technology of China
    ClinicalTrials.gov Identifier:
    NCT05981677
    Other Study ID Numbers:
    • BAM_lab_NSSI_03
    First Posted:
    Aug 8, 2023
    Last Update Posted:
    Aug 8, 2023
    Last Verified:
    Aug 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 8, 2023