Self Injury

6

Review clinical trials related to Self Injury. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Pilot Trial of an Emotion Regulation and Executive Functioning Intervention for Self-Injurious Thoughts and Behaviors (SITBs) in Children

The goal of this study is to develop and test an outpatient intervention for preadolescents (ages 7-12) with self-injurious thoughts and behaviors (SITBs). The main questions it aims to answer are: 1. Does the newer intervention lead to better engagement of families in treatment compared to treatment as usual (TAU)? 2. Is the new intervention feasible, acceptable, and appropriate? 3. Does the new intervention lead to more improvements in SITBs, mental health symptoms, and treatment targets compared to TAU? Preadolescent participants with SITBs and their families will be randomized to either the new intervention or TAU, which will consist of the typical interventions the study therapist would use for preadolescents with SITBs. Participants will: 1. Complete an initial baseline assessment to determine eligibility and assess SITBs, mental health symptoms, executive functioning, and emotion regulation 2. Participate in a \~weekly, outpatient intervention lasting around 3-4 months 3. Complete additional assessments at mid-treatment, post-treatment, and 3-month follow-up 4. Participate in an interview sharing their perceptions of the intervention

Participants needed: 52
Trial details
Age: 7-12Biological sex: AllType: InterventionalSponsor: University of Colorado, DenverUpdated: May 14, 2026
Eligibility criteria

between the ages of 7-12 [+5]

symptoms interfering with ability to participate in assessments/therapy (i.e., p... [+4]

Status: Recruiting

Manualized Assessment and Treatment Model of Challenging Behavior

Despite decades of mounting single-case-design evidence for the efficacy of applied behavior analysis (ABA) and other approaches for the assessment and treatment of challenging behavior, an evidence-based comprehensive approach remains to exist. The current study will collect test the efficacy of a standardized manual for assessing and treating challenging behavior for individuals with severe and mild challenging behavior.

Participants needed: 30
Trial details
Age: 3-17Biological sex: AllType: InterventionalSponsor: Rutgers, The State University of New JerseyUpdated: May 8, 2026Locations: 1
Eligibility criteria

children from ages 3 to 17; [+5]

patients who do not meet the inclusion criteria; [+5]

Status: Recruiting

Basic and Applied Research on Extinction Bursts

Although highly effective, treatments like FCT include extinction, which can have adverse side effects. The extinction burst, an increase in the frequency or intensity of destructive behavior at the start of treatment, is the most common side effect of extinction, and can increase the risk of harm to the patient and others. The goal of the current study is to evaluate the prevalence of extinction bursts when various parameters of reinforcement (i.e., rate, magnitude, quality) are manipulated.

Participants needed: 40
Trial details
Age: 3-17Biological sex: AllType: InterventionalSponsor: Rutgers, The State University of New JerseyUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

children aged 3 to 17; [+5]

patients currently receiving 15 or more hours per week of treatment for their pr... [+4]

Status: Recruiting

Extensions of Resurgence as Choice

Although behavioral treatments for decreasing destructive behavior, such as differential reinforcement of alternative behavior (DRA), are effective in the clinic, problem behavior often returns when a caregiver does not give the child their way in the natural environment (e.g., caregiver is busy with an infant sibling). This form of treatment relapse is known as resurgence. The goal of the current study is to evaluate whether alternating sessions in which the child can have their way (i.e., "on" sessions) with sessions in which the child can not have their way (i.e., "off" sessions) helps to mitigate resurgence.

Participants needed: 30
Trial details
Age: 3-17Biological sex: AllType: InterventionalSponsor: Rutgers, The State University of New JerseyUpdated: Apr 17, 2026Locations: 1
Eligibility criteria

boys and girls from ages 3 to 17; [+5]

patients who do not meet the inclusion criteria; [+5]

Status: Recruiting

Propranolol for Aggression, Self-Injury, and Severe Disruptive Behavior in Adolescents and Adults With Autism

The goal of this clinical trial is to learn if propranolol can help reduce challenging behaviors associated with Autism Spectrum Disorder, including aggression, self-injury, and severe disruptive behaviors. Participants will be randomly assigned to receive either propranolol or a placebo (a look-alike substance that contains no drug) daily for 12 weeks. After the 12 weeks, all participants will have the opportunity to receive propranolol for an additional 12 weeks.

Participants needed: 60
Trial details
Phase: Phase 2Age: 12-40Biological sex: AllType: InterventionalSponsor: Jeremy Veenstra-vanderweeleUpdated: Mar 30, 2026Locations: 2
Eligibility criteria

Age between 12-40 years. [+10]

Those who are unable to provide informed consent and have no parent/guardian/leg... [+17]

Status: Recruiting

Brief Admission by Self-referral for Individuals With Self-harm: Effects on Compulsory Care

Brief Admission by self-referral (BA) is a standardized treatment model, providing patient-controlled and person-centered care. It was developed to reduce self-harm and compulsory care by promoting autonomy. Randomized clinical trials have not yielded significant between group differences with respect to inpatient care, including compulsory care. The major difficulty in evaluating BA is preventing the control group from cross-contamination, as in the implementation process of BA, all physicians, all inpatient and outpatient staff as well as managers need to be informed and undergo basic education regarding the intervention. As BA addresses a prevalent and frustrating issue in psychiatric health care, there is considerable risk that the approach leaks to the control group, reducing the possibility to detect between-group differences. In the current study this will be addressed through a register-based approach, comparing similar clinics, implementing BA at different timepoints over time. Individuals with traits of borderline personality disorder will be included and comparisons will be made with respect to compulsory care, voluntary inpatient care and mortality.

Participants needed: 7,000
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Region SkaneUpdated: Aug 14, 2025Locations: 4Duration: 5 Years
Eligibility criteria

Living in the uptake area of Lund, Linköping, Helsingborg or Norrköping [+2]

not fulfilling inclusion criteria