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Recruiting NCT04211753

Effectiveness and Security Testing of a Mobile App (B·RIGHT) for Emotional Crisis in Borderline Personality Disorder

No phase Interventional Borderline Personality Disorder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Treatment as usual (schema therapy), Mobile app.
Who it may be relevant to
Registry conditions: Borderline Personality Disorder. Basic parameters: 18 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Spain
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effectiveness and Security Testing of a Mobile App (B·RIGHT) for Self-managing Emotional Crises in People With Borderline Personality Disorder: A Pragmatic Randomized Controlled Trial

Overview

To assess the effectiveness and security of a mobile App (beta version) for self-managing emotional crisis in a pragmatic randomized controlled trial with 80 patients with borderline personality disorder (40 patients with treatment as usual, TAU) versus 40 patients with TAU plus the mobile App)

Interventions

  • Behavioral Treatment as usual (schema therapy)
    weekly group psychotherapy and bimonthly individual psychotherapy
  • Device Mobile app
    Medical device for crisis intervention

Primary outcome measures

  • Number of psychiatric.emergencies and hospitalizations [Time frame: 9-month]
  • smartphone addiction [Time frame: 9-month]

Eligibility criteria

Inclusion criteria

  • DSM-5 (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition) of borderline personalidad disorder (BPD)
  • Aged 18-60 yeats old

Exclusion criteria

  • Comorbidity with mental retardation
  • Comorbidity with psychotic disorder
  • Comorbidity with antisocial personality
  • Comorbidity with autism spectrum disorder

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Spain · 1 center
  • Consorci Sanitari del Maresme — Mataró

Identifiers

NCT: NCT04211753 · CEIC 32/16

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗