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College Students Who Self-Harm

College Students Who Self-Harm: An Intervention Study

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02522143
Enrollment
0
Registered
2015-08-13
Start date
2014-02-28
Completion date
2014-12-31
Last updated
2017-06-20

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

Conditions

Borderline Personality Disorder, Suicide

Keywords

self-harm, self-mutilation, cutting

Brief summary

Study Aims/Objectives: This projects' Primary Aim is development of a Condensed DBT Stepped Care Model tailored to the unique requirements of students meeting sub-clinical diagnostic criteria for BPD (Borderline Personality Disorder) with its associated high rate of self-harm and suicide.

Detailed description

Study Aims/Objectives: This projects' Primary Aim is development of a Condensed DBT Stepped Care Model tailored to the unique requirements of students meeting sub-clinical diagnostic criteria for BPD with its associated high rate of self-harm and suicide. The investigator previously implemented a 4-mth condensed-DBT regimen with success in an adult clinical population. This study will evaluate an intensive 8 week intervention formulated for students to reduce the high prevalence of self-harm and dysfunctional behavior in this population and reduce the need for extended treatment in later years. It will include rigorous screening for collateral disorders, including Substance Use Disorders exacerbating BPD symptoms and suicide risk.

Interventions

BEHAVIORALInformational sessions describing BPD characteristics

Control intervention consists of informational sessions describing BPD characteristics/ treatment and time- / stress-management skills

BEHAVIORALCondensed-DBT treatment intervention

The Intervention consists of an 8-week manual based psychoeducational group utilizing modified condensed-DBT Treatment manual previously used in a treatment study (Moen et al, 2012).

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 27 Years
Healthy volunteers
No

Inclusion criteria

* Age 18 to 27 * Currently enrolled in college * Meet at least 4 of 9 Criteria of BPD (DSM-V) with one criterion being self-harm (e.g. cut, burn, or hit self)

Exclusion criteria

* have a current major psychiatric disorder diagnosis, or other gross cognitive impairment (as identified in the phone screen or the SCID I measure) or * have undergone DBT or * are suicidal and require full DBT and/or hospitalization or * are currently in any other individual or group therapy * unable to attend weekly visits over 8 weeks, starting March 24, 2014

Design outcomes

Primary

MeasureTime frameDescription
Change in BPD (Borderline Personality Disorder) behaviors8-weeksproduce greater decreases in depression, anxiety, self-harm, and other BPD behaviors,

Secondary

MeasureTime frameDescription
Change in reported psychiatric symptoms,8-weeksdiminish reported psychiatric symptoms, and Decreased utilization of Emergency Room, crisis, and University Disability Services on campus.
Diminished emergency room visits8 weeksself reported ER visits

Countries

United States

Outcome results

None listed

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