Creation and Setting up of Therapeutic Programs, Interprofessional Communication, Patients' Education and Counseling (EMCIQUAL)

Creation and Setting up of Therapeutic Programs, Interprofessional Communication, Patients' Education and Counseling: a Qualitative Study in 3 Physical Therapy and Rehabilitation Departments

The purpose of this study is to suggest system for improving patients' management through a detail analysis of physical therapy departments functioning

Study Overview

Detailed Description

First phase:

  • Description of the actual patients' management through individual semi directive interviews and focus groups of health professionals, patients, and members of the hospital directory departments.
  • Identification of barriers

Second phase: suggestion of system for improving patients' management

Study Type

Observational

Enrollment (Actual)

63

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Créteil, France, 94010
        • CHU Henri Mondor-Albert Chenevier
      • Garches, France, 92380
        • CHU Raymond Poincaré- Groupement hospitalier universitaire Ouest
      • Paris, France, 75014
        • Cochin Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

In each of 3 centers, we will evaluate :

  • 13 healthcare professionals
  • 8 patients
  • 1 hospital executives

Description

Inclusion Criteria:

  • For doctors: affiliation to physical therapy and rehabilitation departments, age, career and function
  • For other health professionals: affiliation to physical therapy and rehabilitation departments, service length, age, gender
  • For patients: age, gender and therapeutic programs

Exclusion Criteria:

- Persons not wishing to participate

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient management system
Time Frame: 1 year
Qualitative study in the form of semi-structured individual interviews and group meetings (focus group) with health professionals, patients (and members of the hospital management to collect comprehensive information, prior to the formalization and implementation of specific actions.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Serge Poiraudeau, MD, PhD, AP-HP, Descartes University, INSERM

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2012

Primary Completion (Actual)

January 1, 2014

Study Completion (Actual)

July 1, 2014

Study Registration Dates

First Submitted

April 30, 2013

First Submitted That Met QC Criteria

May 3, 2013

First Posted (Estimate)

May 7, 2013

Study Record Updates

Last Update Posted (Estimate)

July 28, 2014

Last Update Submitted That Met QC Criteria

July 25, 2014

Last Verified

July 1, 2014

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Professionals and Patients in the Department of Physical Medicine and Rehabilitation

3
Subscribe