TRANSforming InTerprofessional Cardiovascular Prevention in Primary Care

NCT01418716 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 759

Last updated 2017-02-17

No results posted yet for this study

Summary

The TRANSIT program is a program to TRANSform InTerprofessional clinical practices to improve cardiovascular prevention in primary care. It addresses priorities in primary care relevant to the Chronic Care Model (Wagner 2001): self-management support, delivery-system design, and management of clinical information.

The program includes :

* a case manager to coordinate and provide care and follow up;
* clinical protocols and tools to support interprofessional and systematic follow up;
* training for clinicians;
* patient's personalized cardiovascular health booklet;
* tools to promote group sessions for patient education on cholesterol, hypertension, and diabetes.

The general OBJECTIVE of this trial is to evaluate and compare two STRATEGIES for implementing the TRANSIT program in Family Medicine Groups (FMGs):

1. facilitation, and
2. passive diffusion.

Passive diffusion is the usual strategy where clinicians implement an intervention program by themselves. Facilitation is a strategy whereby a facilitator provides support to a team of clinicians to help them introduce the changes required to implement the program into practice.

The hypothesis is that facilitation will be more efficacious to implement the program than passive diffusion:

* it will enhance the provision of cardiovascular preventive care;
* it will enhance interprofessional collaboration;
* it will enable more efficaciously the implementation of new clinical processes;
* it will improve patient clinical outcomes;
* it will cost more in the short term, but will have positive economic impact in the long term;
* there will be less "undesired effects" of all types related to implementation.

To test the hypothesis, we assess the efficacy of the implementation strategies to enhance interprofessional collaboration and better support patients in the management of their conditions. Impact on provision of care, interprofessional collaboration, clinical processes, and patient clinical outcomes (values, therapeutic targets, and lifestyle habits) will be evaluated. Moreover, the implementation cost related to each strategy will be estimated.

We complement the trial with qualitative methods to document the perceptions of clinicians, facilitators, patients and members of the family regarding the TRANSIT program, the implementation strategies and the observed changes in the clinical practices and outcomes.

Conditions

  • Diabetes Mellitus, Type 2
  • Hypertension
  • Dyslipidemias
  • Cholesterol, LDL
  • Comorbitdity

Interventions

OTHER

Facilitation

Facilitation is a change management process. In the TRANSIT study, the change consist in implementing the TRANSIT program in primary care clinics. In the facilitation group, external facilitators accompany, support, and empower clinical teams so they quickly develop a sense of ownership regarding new clinical practices and sustainably implement them with lower costs. External facilitators offer counseling, coaching, and various tools to an internal facilitation team composed of clinicians of the clinical team to support their efforts in implementing change in their practices. Facilitation activities are structured in a cycle of 4 steps, the Plan-Do-Study-Act cycle (PDSA cycle).

OTHER

Passive diffusion

Clinical teams in primary care clinics implement the TRANSIT program without the help of facilitators.

Sponsors & Collaborators

  • Université de Montréal

    collaborator OTHER
  • Fonds de la Recherche en Santé du Québec

    lead OTHER_GOV

Principal Investigators

  • Lyne Lalonde, Ph.D. · Centre de santé et de services sociaux de Laval ; University of Montreal

  • Johanne Goudreau, Ph.D. · Université de Montréal

  • Céline Bareil, Ph.D. · HEC Montréal

  • Éveline Hudon, M.D. · Université de Montréal

  • Fabie Duhamel, Ph.D. · Université de Montréal

  • Marie-Thérèse Lussier, M.D. · Université de Montréal

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2013-10-31
Completion
2016-10-31

Countries

  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01418716 on ClinicalTrials.gov