eConculta: Impact of Virtual Visits in Primary Care (eConsulta)

February 7, 2011 updated by: Institut Catala de Salut

Before and After Study to Assess the Impact of the Use of Virtual Consultation on Frequency of Patient Attendance, and Satisfaction of Patients and Professionals

eConsulta is a before and after quasi-experimental study without control group and its purpose is to asses the impact of virtual visits in primary care on the frequency of attendance of the patients to the primary care centre. The use of virtual consultations should lower the number of face to face visits to primary care. It also should create satisfaction to both users: primary care professionals and patients.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Excess on primary care face to face demands generates a work overload for the professionals, and it could lead to a lower quality of care and less job satisfaction. Not all primary care demands need a face to face encounter so incorporating new technologies into daily practice care such as communication doctor/nurse-patient through a website could be part of the solution. So we designed a study in order to assess the impact of the use of virtual consultation on frequency of attendance and the satisfaction of patients and professionals with the service.

It is a before after quasi-experimental multi-centre study with no control group. Agreed voluntarily to participate 13 primary care centres, 20 primary care physicians, 17 nurses them having 16.720 reference adult patients. We designed a website where participants can access the internet and consult their doctor/nurse, who will answer within 48 hours at maximum. The intervention will last 6 months.

We believe that the site can be useful by both patient and professional. For some types of patient, the use of the site may increase its accessibility, reduce face to face consultations and improve satisfaction, while the professional makes a more efficient practice.

Study Type

Interventional

Enrollment (Actual)

16720

Phase

  • Not Applicable

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

      • Barcelona, Spain, 08001
        • EAP Gòtic
      • Barcelona, Spain, 08005
        • EAP Ramón Turró
      • Barcelona, Spain, 08018
        • EAP El Clot
      • Barcelona, Spain, 08020
        • EAP Sant Martí
      • Barcelona, Spain, 08027
        • EAP La Sagrera
      • Barcelona, Spain, 08029
        • EAP Montnegre
      • Barcelona, Spain, 08030
        • EAP Sant Andreu
      • Barcelona, Spain, 08032
        • EAP El Carmel
      • Barcelona, Spain, 08032
        • EAP Horta
      • Barcelona, Spain, 08037
        • EAP Pare Claret
      • Barcelona, Spain, 08038
        • EAP Dr. Carles Ribas
      • Barcelona, Spain, 08041
        • EAP Congrés
      • Barcelona, Spain, 08041
        • EAP Guinardó Baix

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

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 18 years or over
  • having a primary care centre assigned
  • to have both physician and nurse participating in the project
  • to use the same electronic clinical recording software

Exclusion Criteria:

  • none

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?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: eConsulta
Those patients who are offered to use the eConsulta, a web where they can virtually consult with their primary care doctor or nurse.
It is a web specifically designed for the project where elected patients can consult virtually with their primary care physician and within 48 hours have an answer.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of primary care face to face visits of the patients during the 6 month intervention, compared to the number of face to face visits of the same patient, in a 6 month previous period.
Time Frame: Visits done from 01/06/2010 to 01/12/2010 compared to the himself the same period 1 or 2 years before (depending on the flu)
Number of face to face visits of each patient (who used the eConsulta web site) to primary care physician or nurse during the 6 months of the intervention (from 01/06/2010 to 01/12/2010) compared to the number of visits of the same patients the same period 1 or 2 years before, depending on the appearance of a swine flu outbreak (2009 if there is a swine flu outbreak or 2008 if there is not). The information source of the number of visits will be the electronic clinical record, which is the same in all the practices participating.
Visits done from 01/06/2010 to 01/12/2010 compared to the himself the same period 1 or 2 years before (depending on the flu)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Measure the doctor/nurse satisfaction
Time Frame: At the end of the study, 01/12/2010

Satisfaction with the whole service with a 10 point scale. Items:

  1. Are you satisfied with the eConsulta?
  2. It is easy to use the web?
  3. Has it been easy to integrate it with the daily practice?
At the end of the study, 01/12/2010
Measure the patient satisfaction
Time Frame: At the end of the study, 01/12/2010

Satisfaction with the whole service with a 10 point scale. Items:

  1. Are you satisfied with the eConsulta?
  2. It is easy to use the web?
  3. Would you use it in the future?
At the end of the study, 01/12/2010

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Josep Casajuana, Institut Català de la Salut
  • Study Chair: Maria A Casas, Institut Català de la Salut
  • Study Chair: Rosa Chumillas, Institut Català de la Salut
  • Study Chair: Mireia Fàbregas, Institut Català de la Salut
  • Study Chair: Ana I Garaikoetxea, Institut Català de la Salut
  • Study Chair: Maria I Garrido, Institut Català de la Salut
  • Study Chair: Yolanda Lejardi, Institut Català de la Salut
  • Study Chair: María J Martínez, Institut Català de la Salut
  • Study Chair: Maria C Piorno, Institut Català de la Salut
  • Study Chair: Joan Camús, Institut Català de la Salut

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

Helpful Links

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

January 1, 2009

Primary Completion (Actual)

December 1, 2010

Study Completion (Actual)

December 1, 2010

Study Registration Dates

First Submitted

May 11, 2010

First Submitted That Met QC Criteria

May 17, 2010

First Posted (Estimate)

May 18, 2010

Study Record Updates

Last Update Posted (Estimate)

February 8, 2011

Last Update Submitted That Met QC Criteria

February 7, 2011

Last Verified

January 1, 2011

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.

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