Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
All Genders
NCT07213492

Multimodal Intervention to Support Hospital-to-Community Transition in Bipolar Disorder

Led by McMaster University · Updated on 2026-01-14

10

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

Sponsors

M

McMaster University

Lead Sponsor

S

St. Joseph's Healthcare Hamilton

Collaborating Sponsor

AI-Summary

What this Trial Is About

People with bipolar disorder (BD) are at high risk of relapse following hospital discharge, partly due to a lack of BD-specific expertise and resources within community services required for comprehensive treatment. Although clinical guidelines recommend combining medication and psychosocial support, and research shows that early intervention is associated with improved outcomes, no structured care programs currently exist for individuals in the early stages of BD, contributing to chronic illness progression and preventable hospitalizations. This open-label pilot trial will assess the feasibility, acceptability, and preliminary effectiveness of a structured care pathway to support the transition from hospital to community care. The intervention includes group-based psychoeducation, individual peer support, and personalized support for community healthcare providers to improve illness insight, treatment adherence, and symptom management.

CONDITIONS

Official Title

Multimodal Intervention to Support Hospital-to-Community Transition in Bipolar Disorder

Who Can Participate

Age: 18Years - 35Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient-participants must be between 18 and 35 years old.
  • Must have been diagnosed with bipolar disorder within the past 24 months.
  • Must have experienced psychosis and/or a lack of insight into their illness at the time of enrollment.
  • Must be able to understand and speak English.
Not Eligible

You will not qualify if you...

  • Individuals with a severe psychiatric condition that would prevent them from safely engaging in the intervention.
  • Those with significant cognitive impairment or a medical condition that interferes with their ability to participate in psychoeducation or peer-support sessions.
  • Individuals with an active substance use disorder that may impact adherence to the intervention.
  • Participants who do not speak English and are unable to engage in study sessions without language support.
  • Individuals who are already enrolled in another structured psychoeducational or peer-support program that could interfere with study outcomes.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

St. Joseph's Healthcare Hamilton

Hamilton, Ontario, Canada, L8N 3K7

Actively Recruiting

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Research Team

F

Fabiano A. Gomes, MD, Ph.D.

CONTACT

D

Daniela Giansante, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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