Unified Protocol for Treatment of Emotional Disorders in Brief Groups in Primary Care Services in Spain

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorInstituto de Investigación Sanitaria Aragón

About this trial

The aim of this project is to contribute to the improvement of psychological care received in primary care (PC), through the study of the cost-effectiveness and acceptability of the Unified Protocol for the treatment of emotional disorders in brief groups in primary care services in Spain (PU-AP) for the treatment of emotional disorders (EDs), the most prevalent in our society. To do so, a pilot study will be carried out, and, subsequently, a randomized clinical trial to study the efficacy, cost-effectiveness and acceptability of the Unified Protocol for the transdiagnostic treatment of EDs, applied in 5 or 8 group sessions. Finally, the researchers will analyze whether there are specific patient profiles that will benefit more from one or the other condition. The results will contribute to the personalization of the psychological treatment of users with EDs attending PC in the Spanish public health system.

Eligibility criteria

Qualifiers

Have at least one EDs diagnosis (anxiety, depressive, obsessive-compulsive, trauma and somatic disorders) from the ADIS-5 interview

Have a score between 0 and 5 severity (mild-moderate) on the diagnoses on the CSR of the ADIS-5

Be able to attend all assessment and treatment sessions

Individuals on pharmacological treatment will be asked to maintain the dosage for the duration of the study, unless there is a medical contraindication

Disqualifiers

Absence of clinical diagnosis

Presenting a diagnosis of EDs with a severity score on diagnoses between 6 and 8 on the ADIS-5 CSR (severe) or a clinical condition requiring specialized mental health intervention such as presence of severe mental disorder (e.g., personality disorder, bipolar disorder, or schizophrenia), suicide risk at the time of assessment, or substance use in the past three months

Who have received 8 or more sessions of CBT (during the past five years) with techniques such as cognitive flexibility or exposure

Who are receiving psychological treatment.

Trial design

Treatments tested in this trial

  • 5-session UP condition
  • 8-session UP condition

Treatment groups

180 Participants
are divided into 2 treatment groups

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

Centro de Salud Carinyena, Hospital Universitario de La Plana Status unavailable 12540, Villarreal, ValenciaSpainSpain