700 Participants Needed

Care Transitions Program for Dementia

PM
MA
Overseen ByMartyne Audet, MSc
Age: 65+
Sex: Any
Trial Phase: Academic
Sponsor: Laval University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 1 JurisdictionThis treatment is already approved in other countries

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to enhance care coordination for individuals with major neurocognitive disorders, such as Alzheimer's, and their caregivers. It introduces the CoMPAS+ MNCD Program to streamline communication and support between healthcare providers and patients. The trial evaluates this program in various regions to assess its impact on care transitions, aiming to make the healthcare experience smoother for everyone involved. Individuals dealing with major neurocognitive disorders who have used healthcare services within the last six months might be suitable candidates for this trial. As an unphased trial, this study offers a unique opportunity to contribute to innovative care solutions and potentially improve the healthcare experience.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the research team or your doctor.

What prior data suggests that the CoMPAS+ MNCD Program is safe for improving care transitions?

Research has shown that the CoMPAS+ MNCDs Program has been adjusted to improve the transition of care for people with major neurocognitive disorders (MNCDs). Previous studies found that the CoMPAS program can boost the well-being of people living with dementia and their caregivers, indicating that the program is generally safe and well-received.

This trial is labeled as "Not Applicable" in terms of phases, meaning it focuses on improving care coordination and processes rather than testing a new drug or medical device. Therefore, it does not carry the usual safety risks associated with trials for new medications. The main aim is to enhance how care is managed and delivered, which typically does not involve direct risks to participants.123

Why are researchers excited about this trial?

Researchers are excited about the CoMPAS+ MNCDs Program because it offers a fresh approach to managing dementia care transitions. Unlike traditional treatments that focus mainly on medications or isolated healthcare interactions, this program emphasizes coordinated workshops involving health professionals and caregiver partners across different care settings. This approach aims to enhance communication and collaboration between hospitals, primary care, and home care services, potentially leading to more seamless care experiences for patients. By integrating various healthcare providers, the program seeks to reduce hospital visits and improve overall care quality for individuals with dementia.

What evidence suggests that the CoMPAS+ MNCDs Program could be effective for improving care transitions in dementia?

Research has shown that the CoMPAS+ program, which participants in this trial may experience through various local service networks, can improve the transition of care for patients with major memory disorders, such as Alzheimer's disease. Studies have found that programs like CoMPAS+ enhance communication and teamwork among healthcare providers, leading to better outcomes for patients and their caregivers. Specifically, the program has successfully enhanced the well-being of people with dementia and their caregivers by promoting communication focused on the individual. This ensures that care is tailored to the patient's specific needs and preferences. These improvements in care coordination can lead to a smoother healthcare experience for patients and their families.245

Who Is on the Research Team?

PM

Patrick M Archambault, MD, MSc, FRCPC

Principal Investigator

Laval University

Are You a Good Fit for This Trial?

This trial is for older adults with major neurocognitive disorders like Alzheimer's, and their caregivers. It focuses on improving care transitions between healthcare providers to enhance coordination and support.

Inclusion Criteria

Consent to the research team collecting data from the medical records of the person being cared for (FMG Electronic Medical Record (EMR) when accessible, Hospital Electronic Patient Record (EPR) when accessible, etc.)
Be a participant in the CoMPAS+ MNCD workshops and be part of at least one of the following categories of participants: Health professionals working in a CISSS CA health facility or with a community organization, CISSS CA decision-makers or local managers, Community service representative (e.g., Alzheimer's Society, L'APPUI)
Be able to consent independently to research and reside at home, in a retirement home, in an intermediate residence, or a family-type resource
See 4 more

Exclusion Criteria

I do not agree to share my medical records for this trial.
User living in a provincial long-term care facility at the time of recruitment
I am over 65, have a significant memory or thinking problem, and cannot consent to research on my own without a caregiver.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Implementation

Implementation of the CoMPAS+ MNCD Program through workshops and interventions in Local Services Networks

12-15 months
Multiple workshops and interventions

Follow-up

Participants are monitored for the impact of the Program on care transitions, quality of life, and caregiver burden

15 months
Telephone questionnaires at multiple time points

Evaluation

Evaluation of the Program's sustainability and scale-up potential through focus groups and interviews

12-15 months

What Are the Treatments Tested in This Trial?

Interventions

  • CoMPAS+ MNCDs Program
Trial Overview The CoMPAS+ MNCDs Program is being tested, which aims to improve the quality of care transitions for patients with neurocognitive disorders through better practices and local solutions in Family Medicine Groups.
How Is the Trial Designed?
3Treatment groups
Experimental Treatment
Group I: Local Services Network (LSN) Montmagny-L IsletExperimental Treatment1 Intervention
Group II: Local Services Network (LSN) BellechasseExperimental Treatment1 Intervention
Group III: Local Services Network (LSN) Alphonse-DesjardinsExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Laval University

Lead Sponsor

Trials
439
Recruited
178,000+

Institut national d'excellence en santé et service sociaux

Collaborator

Trials
1
Recruited
700+

CISSS de Chaudière-Appalaches

Collaborator

Trials
9
Recruited
16,500+

Published Research Related to This Trial

Older adults with dementia experience significantly higher rates of nursing facility use, hospitalizations, and transitions in care compared to those without a dementia diagnosis, indicating a complex care trajectory.
Most transitions to nursing facilities for individuals with dementia occur after hospitalizations, highlighting the interconnectedness of care settings and the need for coordinated support during these transitions.
Transitions in care for older adults with and without dementia.Callahan, CM., Arling, G., Tu, W., et al.[2022]
A partnership project aimed at improving care transitions for hospitalized seniors was implemented, focusing on three key levels: organizational agreements, unit-level adjustments, and individual care plans.
The project included tools like a transition checklist and customized supports, which helped enhance acceptance and facilitate safer transitions for seniors with complex medical and mental health needs.
Improving transitions between acute mental health and residential care.McLennan, M., Kurucz, S., Fudge, H.[2019]
A study analyzing discharge documentation for 60 older adults with dementia revealed that only 17% of the documentation met excellent standards for transitional care needs, indicating significant gaps in the quality of information provided during care transitions.
The variability in discharge documentation quality (37% excellent, 43% adequate, and 20% poor) highlights the urgent need for improvements to ensure safe and effective care for individuals with dementia moving from hospital to nursing home settings.
Analysis of discharge documentation for older adults living with dementia: A cohort study.Parker, KJ., Phillips, JL., Luckett, T., et al.[2021]

Citations

Study Details | NCT06608589 | CONSTELLATIONS Living ...In this study, the investigators adapt COMPAS+ to focus on improving care transitions for patients with major neurocognitive disorders (MNCDs) and their ...
Efficacy of COMPAs, an App Designed to Support ...Conclusions: COMPAs intervention improved well-being in persons living with dementia and their caregivers by developing person-centered ...
3.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/38963691/
Efficacy of COMPAs, an App Designed to Support ...COMPAs intervention improved well-being in persons living with dementia and their caregivers by developing person-centered communication within the dyad.
Improving the Care Transitions of Older Adults Living with ...In this study, the investigators adapt COMPAS+ to focus on improving care transitions for patients with major neurocognitive disorders (MNCDs) and their ...
RePORT ⟩ RePORTERWe're sorry but RePORTER doesn't work properly without JavaScript enabled. Please enable it to continue.
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security