Under construction – not a live service
Sign in
Taking people in SpainNo phase

Digital Platform Tested to Support Care in Early Psychosis Programme

Tests a digital platform to help young adults with early psychosis stay in care.

Plain-language title generated from the registry record
Registry title: Effectiveness of a Digital Platform in Engagement and Prognosis of Patients in an Early Intervention Pychosis Programme

Key facts

Where
Sant Boi de Llobregat, SpainSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 40 years old?

Source: NCT06556251, who can take part

Where in Spain

  • Parc Sanitari Sant Joan de DéuSant Boi de Llobregat, SpainTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Fundació Sant Joan de Déu
Trial code
NCT06556251
Record updated
25 May 2025
Original description
This is a randomised, prospective, controlled trial in which one group (experimental group; GE) receives access to the PIPPEP (Intervention Programme for Early Psychosis) platform in addition to the treatment as usual (TAU) in PIPPEP, while the other group (control group; GC) receives only TAU in PIPPEP.Read full original descriptionShow less

Evaluating the Effectiveness of a Digital Platform in the Engagement and Prognosis of Patients in the Early Intervention Programme in Psychosis

This is a randomised, prospective, controlled trial in which one group (experimental group; GE) receives access to the PIPPEP (Intervention Programme for Early Psychosis) platform in addition to the treatment as usual (TAU) in PIPPEP, while the other group (control group; GC) receives only TAU in PIPPEP.

Main objective:

- To assess whether the use of the PIPPEP platform improves psychosocial and pharmacological treatment adherence in mental health programmes.

Secondary objectives:

* To assess the cost-effectiveness of the PIPPEP app. * Evaluation of the dissemination of the platform. * To assess the clinical and functional outcomes of patients using the PIPPEP platform in terms of 1) positive symptoms, 2) side effects of antipsychotic medication, 3) perceived social self-stigma, 4) risk assessment, 5) comorbid symptoms and 6) social functioning

The participants are 1) between 18 and 40 years of age, who are being treated in one of the PIPPEP programmes for early intervention in psychosis at Sanitary Parc Sant Joan de Déu and who meet the inclusion criteria "extremely high risk of psychosis", "critical phase or "first psychotic episode" and 2) agree to participate in the study and sign the informed consent form.

Inclusion: Age between 18 and 40 years; Fulfil the criteria for one of the three groups (First Psychotic Episodes, Critical Period or Ultra High Risk of Psychosis; UHR); To undergo community-based treatment as part of one of our facility's early intervention programmes for psychosis; Have signed the informed consent form for the study.

Exclusion: Have had a medical condition that better explains the psychotic symptoms; No mobile phone/laptop/tablet to use the platform; Lack of skills and/or knowledge to use the platform; Not have knowledge of the Catalan or Spanish language; Have a diagnosed mental disability (premorbid Intelligence Quotient <70).

ClinicalTrials.gov NCT06556251