Integrated care program for managing depression
Integrated Depression Care Project
This study tests a new program that helps people with depression by improving how doctors and healthcare workers work together and providing better support for patients to manage their own care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 150 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | University Ghent Academic / other |
| Locations | 2 sites (Mechelen and 1 other locations) |
| Trial ID | NCT05788198 on ClinicalTrials.gov |
What this trial studies
The Integrated DEpression CAre (IDECA) Programme is designed to enhance the management of depression through a comprehensive intervention strategy. It includes the development of a shared care protocol that integrates primary, secondary, and tertiary care levels, along with training modules for healthcare providers and case managers. Additionally, the program offers patient education for self-management of depression and proposes a financing model for integrated care. The effectiveness of this approach will be evaluated through various clinical outcome indicators.
Who should consider this trial
Good fit: Ideal candidates for this program are individuals aged 18-65 who present with depressive symptoms at a general practitioner's office.
Not a fit: Patients with severe depression requiring immediate referral to specialized services may not benefit from this integrated care approach.
Why it matters
Potential benefit: If successful, this program could significantly improve the management and outcomes of depression for patients across different care levels.
How similar studies have performed: Other studies have shown promise in integrated care approaches for depression, suggesting potential for success in this program.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * persons between 18-65 * presenting to the general practitioner's office * with depressive symtomatology Exclusion Criteria: * Severe depression warranting direct referral to specialized services Inclusion criteria are kept broad on purpose as it's one of the research questions to define for which patients the intervention (namely the case management) is appropriate.
Where this trial is running
Mechelen and 1 other locations
- ELZ Mechelen-Katelijne — Mechelen, Belgium (Recruiting)
- ELZ Voorkempen — Zoersel, Belgium (Recruiting)
Study contacts
- Principal investigator: Liesbeth Borgermans, PhD — University Ghent
- Study coordinator: Ruben P Willems, PhD
- Email: ruben.willems@ugent.be
- Phone: +32488307749
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.