GPS Project Evaluation of the Impact of the Reorganization of Work Into a Family Medicine Group on Pharmacotherapy and Support for the Autonomy of Seniors With Major Neurocognitive Disorders

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorCHU de Quebec-Universite Laval

About this trial

The model of care tested in the GPS project aims to optimize pharmacotherapy for seniors undergoing cognitive assessment or suffering from major neurocognitive disorder (MCND) at home. The goal is to reduce polymedication, inappropriate medications and the treatment burden of seniors and to maintain their cognitive health, quality of life and autonomy. The intervention will include knowledge exchange sessions with nurses, pharmacists, and doctors in FMGs, and increased collaboration between these professionals and home care services teams. Other goal is to increase the satisfaction of the seniors, their families, and the professionals involved in the GPS project.

Eligibility criteria

Qualifiers

All seniors (65 years of age or older) undergoing cognitive evaluation OR referred to a memory clinic OR having been diagnosed with cognitive impairment within the last year OR with MCND and followed up at home AND,

referred to the pharmacist, for the FMGs exposed

taking prescription medications

Disqualifiers

Seniors in palliative care OR

unable to answer questionnaires in French AND without a caregiver.

Trial design

Treatments tested in this trial

  • GPS clinical intervention

Treatment groups

400 Participants
are divided into 2 treatment groups

Sponsors and collaborators

CHU de Quebec-Universite Laval

Lead sponsor

CISSS de Chaudière-Appalaches

Collaborator

Ciusss de L'Est de l'Île de Montréal

Collaborator

Fonds de la Recherche en Santé du Québec

Collaborator