Application and Effectiveness of the STEPPS in Patients with BPD, Extending to Their Famil
The present research project is framed within the issue of Borderline Personality Disorder (BPD). This condition stands as one of the most common challenges encountered within the mental health services of the National Health System. The primary objectives of this research are to verify whether the combined use of esta
| Condition(s) | Borderline Personality Disorder (BPD) |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | The present research project is framed within the issue of Borderline Personality Disorder (BPD). This condition stands as one of the most common challenges encountered within the mental health services of the National Health System. The primary objectives of this research are to verify whether the combined use of established treatments for patients and their families, conducted in parallel, leads to a greater improvement in patients and their families, respectively. Additionally, another aim of the project is to assess efficiency, defined as the acceptance of intervention programs by patients, their families, and clinical professionals, as well as to demonstrate their feasibility. |
| Who can participate | PATIENTS Inclusion Criteria: * Being at least 18 years old. * Be a patients with symptoms compatible with a diagnosis of BPD who is undergoing treatment or follow-up in someone of the indicated recruitment centers. * Sign an informed consent. Exclusion Criteria: * The presence of any pathology that prevents carrying out the intervention: major depression, psychosis, schizophrenia, substance dependence, eating disorders, another personality disorder, borderline IQ, etc., which due to its severity is currently interfering. FAMILIES: Inclusion Criteria: * Being at least 18 years old. * Be a relative of someone of the patients with symptoms compatible with a diagnosis of BPD who is undergoing treatment or follow-up in someone of the indicated recruitment centers. * Sign an informed consent. Ex |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Universitat Jaume I |
| Locations | Castellon, Spain, Spain |
| Start date | 2024-01-02 |
| NCT ID | NCT06195553 |
| Official listing | https://clinicaltrials.gov/study/NCT06195553 |