Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID05945277

Effectiveness of the Critical Time Intervention-Peer Support Model for People With Serious Mental Illness After Psychiatric Hospital Discharge in Portugal

Led by Lisbon Institute of Global Mental Health - LIGMH · Updated on 2024-07-01

60

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

Sponsors

L

Lisbon Institute of Global Mental Health - LIGMH

Lead Sponsor

C

Columbia University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the Critical Time Intervention-Peer Support (CTI-PS) model, a recovery-oriented mental health program designed for people with serious mental illness such as psychotic disorders, schizophrenia, bipolar disorder, and schizoaffective disorder. This intervention focuses on individuals discharged from inpatient psychiatric treatment facilities, aiming to support their recovery by addressing the consequences of illness and promoting empowerment during a vulnerable transition period. The study is a pilot randomized controlled trial conducted in Portugal to assess the feasibility, implementation, and potential effectiveness of CTI-PS compared to usual care. The CTI-PS intervention is delivered by trained Community Mental Health Workers and Peer Support Workers who use their lived experience to support participants. The program lasts nine months and involves phases called Initiation, Try-Out, and Transfer of Care. Participants in the intervention group receive CTI-PS services alongside usual care. The goal is to help participants build lasting connections with formal and informal support systems, overcome barriers, and strengthen autonomy without becoming their primary source of care. Participants will be involved in the study for up to 18 months, with assessments at the start, 9 months, and 18 months. Researchers will evaluate outcomes such as quality of life, needs assessment, psychopathology, disability level, recovery orientation, self-stigma, and substance use using various standardized tools. Regular supervision of the intervention providers will be conducted throughout the study. The trial aims to explore how well CTI-PS can be implemented in Portugal and contribute knowledge about peer support models globally.

CONDITIONS

Brief Title

Critical Time Intervention-Peer Support

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 65 years
  • Diagnosed with any psychotic disorder based on ICD-10 criteria, including schizophrenia, bipolar disorder, or schizoaffective disorder
  • Discharged from inpatient psychiatric treatment facilities within the month prior to recruitment
Not Eligible

You will not qualify if you...

  • Active suicidal thoughts
  • Cognitive, neurological, or sensory conditions that would interfere with interview assessments

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 9 months

Participants receive Critical Time Intervention-Peer Support services in addition to usual care for 9 months after discharge from inpatient psychiatric treatment. This intervention provides practical and emotional support and helps develop connections to community and health services.

Regular contact with support workers throughout the 9-month period

Follow-up

Duration - Up to 18 months

Participants are monitored for outcomes related to mental health, disability, recovery orientation, self-stigma, and substance use for up to 18 months after starting the intervention.

Periodic assessments during the follow-up period

Trial Site Locations

Total: 3 locations

1

Centro Hospitalar Lisboa Ocidental

Lisbon, Portugal

Actively Recruiting

2

Centro Hospitalar Universitário Lisboa Norte

Lisbon, Portugal

Actively Recruiting

3

Hospital Beatriz Ângelo

Loures, Portugal

Actively Recruiting

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Research Team

M

Manuela Silva, M.D., PhD

M

Margarida Dias

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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