- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05981612
Impact of Emotional Reactivity on Dysfunctional Decision-Making in NSSI Adolescents
April 9, 2024 updated by: Benjamin Becker, University of Electronic Science and Technology of China
Effects of Emotional Reactivity on Decision-Making in Adolescents With Nonsuicidal Self-Injury
Nonsuicidal self-injury (NSSI) is defined as direct, intentional physical injury without suicidal intention.
Studies revealed that dysfunctional interpersonal relationships and reward-related decision-making may play crucial roles in this maladaptive behavior, especially in adolescents.
These interpersonal decision contexts are characterized by constant updating of expectations of rewards and the actual received rewards as well as the associated emotional reactions.
These processes have recently been computationally formalized as prediction errors (PE), specifically reward PEs, valence PEs, and arousal PEs (Heffner et al., 2021; Nat Hum Behav).
In the current study, the investigators aim to investigate whether these PEs make discernible contributions to social decisions in the context of unfair experiences among adolescents with NSSI and matched healthy control adolescents (HC).
Specifically the investigators hypothesized that: 1) reward and emotional PEs show significant predictions of punishment decisions in both groups, 2) however, compared to HC adolescents, the NSSI group will exhibit selective dysfunctions in emotional but not reward PEs leading to punish a norm proposer who provided unfair offers.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
80
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Benjamin Becker
- Phone Number: +86.028-61830867
- Email: ben_becker@gmx.de
Study Locations
-
-
Sichuan
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Chengdu, Sichuan, China
- Recruiting
- Sichuan Provincial Center for Mental Health, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China
-
Contact:
- Lyuan Li
- Email: lly_psychology@163.com
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-
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
- Child
- Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Treatment-seeking NSSI individuals will be recruited from local hospitals and HC from the community.
Description
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)
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 |
|---|
|
NSSI
|
|
HC
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reward prediction errors (PEs)
Time Frame: About 20 minutes
|
Reward PEs will be calculated by the differences between the experienced (when be offered) reward and predicted (before the offer) reward.
|
About 20 minutes
|
|
Valence prediction errors (PEs)
Time Frame: About 20 minutes
|
Valence PEs will be calculated by the differences between the experienced emotional valence and predicted emotional valence.
|
About 20 minutes
|
|
Arousal prediction errors (PEs)
Time Frame: About 20 minutes
|
Arousal PEs will be calculated by the differences between the experienced emotional arousal and predicted emotional arousal.
|
About 20 minutes
|
|
The prediction of PEs of punishment decisions
Time Frame: About 20 minutes
|
All PEs and groups (NSSI, HC) will be used in a regression model to examined whether there is any alteration in the NSSI group when PEs are predicted to punishment (reject) decisions.
|
About 20 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
December 6, 2023
Primary Completion (Estimated)
July 1, 2026
Study Completion (Estimated)
July 1, 2027
Study Registration Dates
First Submitted
July 20, 2023
First Submitted That Met QC Criteria
August 4, 2023
First Posted (Actual)
August 8, 2023
Study Record Updates
Last Update Posted (Actual)
April 11, 2024
Last Update Submitted That Met QC Criteria
April 9, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BAM_lab_NSSI_04
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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