Integration of Chronic Disease Rehabilitation Services Into Primary Care

NCT01319656 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 326

Last updated 2021-09-29

No results posted yet for this study

Summary

The aim of PR1MaC is to establish a clinical intervention that will adapt and permanently integrate rehabilitation services into primary care settings, which would be the reference point in the health care system for people with Chronic diseases (CD). More specifically, the intervention will aim to: (1) clinically operationalize the mechanisms and tools necessary for delivery of integrated CD services, promoting continuity of care in response to the needs expressed by stakeholders; (2) implement and deploy rehabilitation services adapted to the realities of various clinical primary care settings and develop tools to ensure the sustainability of interventions beyond the rehabilitation period; and (3) support clinical primary care teams in the acquisition and maintenance of evidence-based practices for the targeted CDs.

Conditions

Interventions

BEHAVIORAL

Support, management, educational, counselling, follow-up

The project offers a range of activities (educational, counselling, follow-up) by several professionals. The varied range of services is spread out over six months and may include individual or group meetings with professionals. Informational documents and follow-up tools are provided to patients based on their condition, to facilitate the acquisition and maintenance of knowledge, self-management, and changes in risk behaviour.

Sponsors & Collaborators

  • Pfizer

    collaborator INDUSTRY
  • Fonds de la Recherche en Santé du Québec

    collaborator OTHER_GOV
  • Ministere de la Sante et des Services Sociaux

    collaborator OTHER
  • Centre de santé et de services sociaux de Chicoutimi

    collaborator OTHER
  • Centre de santé et de services sociaux de Jonquière

    collaborator OTHER
  • Martin Fortin

    lead OTHER

Principal Investigators

  • Martin Fortin, MD, M.Sc. · Université de Sherbrooke

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2012-07-31
Completion
2013-11-30

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 NCT01319656 on ClinicalTrials.gov