Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07211750

Integrated Care for Older Adults With Major Depression and Physical Multimorbidity - The I-CONNECT

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
82 (estimated)
Sponsor
KU Leuven · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to learn if I-CONNECT (Integrated Care for Older Adults with Major Depression and Physical Multimorbidity) can improve the health and well-being of older adults with depression or bipolar disorder and at least two chronic physical conditions, such as diabetes or high blood pressure. It will also study if the care model improves how people experience their care, lowers treatment burden, and how well the program is delivered. Researchers will compare two groups: I-CONNECT group: participants receive care coordination, a personalized care plan, medication review, shared decision-making support, and regular follow-up from a care coordinator working with their GP, psychiatrist, pharmacist, and specialists. Usual care group: participants continue with their normal healthcare from their GP and psychiatrist. Participants will: Receive either I-CONNECT or usual care, depending on their group Complete questionnaires about their mood, quality of life, and care experience Have their healthcare use (emergency visits and hospitalizations) tracked during the study

Detailed description

Mood disorders, including depression and bipolar disorder, are common in older adults and frequently occur alongside multiple long-term physical health problems. This combination worsens quality of life, raises mortality risk, and increases healthcare use and costs. Despite the high burden, healthcare systems often provide fragmented care, with limited coordination between providers and underuse of mental health resources. I-CONNECT is a person-centered integrated care model designed to address these challenges. It combines professional care coordination with structured medication review, active involvement of general practitioners, psychiatrists, pharmacists, and specialists, and support for self-management through shared decision-making. By bridging primary and mental healthcare, the model seeks to reduce fragmentation, strengthen continuity of care, and improve outcomes for older adults with complex needs. Study Objectives The primary objective is to test whether I-CONNECT improves overall health outcomes compared with usual care. Secondary objectives are to examine participants' experiences of care, the burden of managing multiple health problems, and the impact on healthcare utilization. Hypothesis The investigators hypothesize that the I-CONNECT intervention will: Improve both mental and physical health outcomes, Reduce treatment burden and stress for participants, Enhance satisfaction with care, and Support a more efficient use of healthcare resources. Implementation Evaluation In addition to effectiveness, the study will assess how I-CONNECT is implemented. Process measures will include fidelity to the care model, the amount of intervention delivered, and outcomes of medication reviews. Qualitative feedback from participants and providers will help identify barriers and facilitators to scale-up and sustainability.

Conditions

Interventions

TypeNameDescription
OTHERintegrated care intervention tailored to the needs of older adults leaving at home with mood disorders and multimorbidity in LeuvenThe six guiding principles are translated into practice through a structured six-step care model. Each step operationalizes one or more principles, ensuring that the model is consistently applied across patient trajectories. The program takes 12 months, with flexible contacts depending on patient's needs.

Timeline

Start date
2025-10-01
Primary completion
2026-10-01
Completion
2027-10-30
First posted
2025-10-08
Last updated
2025-12-12

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT07211750. Inclusion in this directory is not an endorsement.