Efficacy of "DBT-LIVE", an Identity Skills Training Program, for Borderline Personality Disorder.

Starting soon · Not applicable

Conditions studied: Treatment 1:Dialectical Behavior Therapy (DBT), Treatment as Usual

In brief

The main objective of this project is to adapt and evaluate the LIVE Skill module in the Spanish population. LIVE Skill is a psychological intervention protocol specifically designed to address identity disturbances in individuals with Borderline Personality Disorder (BPD). The project aims to examine its effectiveness in reducing identity disturbances, emotional regulation difficulties, and suicidal behavior, as well as in improving self-compassion, meaning in life, and personality functioning. In addition, the efficiency and feasibility of the program will be assessed by evaluating its acceptability among both patients and professionals, and its dissemination will be promoted to maximize its clinical impact. The methodology includes a sample of approximately 112 individuals diagnosed with BPD, recruited through the Valencian Association for Personality Disorders (ASVA-TP), who will be allocated into two groups. The project is structured into five studies. First, a qualitative pilot feasibility study will be conducted with approximately 30 participants through focus groups and interviews in order to refine the intervention protocol. The second study will describe the randomized clinical trial protocol, including the interventions and assessment procedures. Subsequently, a randomized controlled trial (RCT) will be carried out, comparing LIVE Skill with treatment as usual (TAU), with assessments conducted at pre-treatment, post-treatment, and six-month follow-up. Following the trial, a qualitative evaluation will be undertaken to identify treatment facilitators and barriers. Finally, the psychometric validation of the questionnaires used in the study will be conducted. The protocol will collect sociodemographic data and measures of identity, emotional regulation, self-compassion, meaning in life, suicidal ideation and behavior, personality functioning, as well as treatment acceptability and feasibility. Participants will provide informed consent and complete an initial assessment to confirm eligibility according to the inclusion and exclusion criteria.

Key facts

Study ID

NCT07684872

Run by

Universidad Europea de Valencia

People needed

112

Starts

2027-01-01

Expected to finish

2028-12-31

Last updated by the study team

2026-07-06

Who can join

Age: 16 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Being 16 years old or more.
• Having the diagnosis of Borderline Personality Disorder.
• Currently receiving treatment or follow-up care at the recruitment center mentioned above.
• Signing the informed consent form to participate in the study; in the case of minors, consent must be provided by parents or legal guardians.

You may not qualify if…

• Individuals with severe conditions that may interfere with participation in the research-such as psychosis, schizophrenia, or intellectual disability.
• Individuals with high substance use who are not in optimal condition to follow the treatment program.
• Individuals who present an imminent risk of suicide or who are not in adequate psychological condition to participate in the program.

Where it is running

• Valencia — Valencia, Valencia, Spain

Full record on ClinicalTrials.gov

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