The mCME Project:Delivering Continuing Medical Education for Community Health Workers Via SMS Text Messages (mCME project)

January 11, 2016 updated by: Christopher J. Gill, Boston University
Community health workers (CHWs) provide essential basic medical care to hundreds of millions of people across the globe. CHWs offer a myriad of services including community sanitation, breast feeding counseling, family planning, management of febrile children, and malaria control and prevention, to name but a few. In fact, CHWs are often the only source of primary health care available to some of the most disadvantaged populations in the world. However, to be effective, CHWs must be trained - and retrained - at regular intervals, and the costs for such trainings can be substantial. In the US, clinicians are required to stay current and maintain their competence through continuing medical education (CME). Increasingly, CME activities are delivered via internet-based, self-teaching modules. A typical example would be a set of topical readings followed by multiple-choice questions, with the answers, and CME credit, provided to the user upon satisfactory completion of the module. This content is typically delivered over the Internet. However, there is no intrinsic reason why this approach could not be adapted so that CME activities are delivered using standard cell phones via SMS text messaging. This would significantly expand professional training opportunities to a far greater range of CHWs than possible through computer/tablet/smart phone platforms, and would be particularly valuable in poorer countries with limited training budgets. In the mCME project, the investigators propose to test the effectiveness and cost effectiveness of a mobile phone-based CME delivery strategy among Vietnamese community-based physician assistants (CBPAs), a cadre of CHW mandated to provide primary health care to rural and disadvantaged populations. The investigators hypothesize that providing CME activities over a mobile platform will significantly improve their professional knowledge, and may also improve their job satisfaction and self-efficacy.

Study Overview

Study Type

Interventional

Enrollment (Actual)

638

Phase

  • Not Applicable

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 to 99 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Graduated from a CBPA training program
  2. Possesses their own cell phone
  3. Phone able to send/receive text messages
  4. Aged 18 years or older

Exclusion Criteria:

  1. Unwilling to sign informed consent
  2. Lives/operates in an area without cellular coverage
  3. Unwilling to be randomized
  4. Unwilling to adhere to study procedures

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Group 1
Weekly non-medical SMS messages
Experimental: Group 2
Receipt of a daily SMS text message describing various aspects of clinical practice
Group 2 subjects receive a daily SMS bullet point, summarizing a key clinical point pertinent to the CBPA's daily work.
Other Names:
  • non interactive model CME
Experimental: Group 3
Receipt of a daily SMS text message describing various aspects of clinical practice, but phrased as multiple choice question
Group 3 subjects receive a c phrased as a multiple choice question. The content mirrors that of group 2, but is presented as a question to render it interactive
Other Names:
  • Interactive model CME

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Medical knowledge (Score on medical knowledge exams)
Time Frame: 6 months
Score on medical knowledge exams administered at baseline and at the end of six months of the intervention
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Job satisfaction (Score on likert scale)
Time Frame: 6 months
Score on likert scale measuring job satisfaction
6 months
Self efficacy (Score in likert scale)
Time Frame: 6 months
Score in likert scale measuring self efficacy
6 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
cost effectiveness analysis of the mCME intervention in terms of costs to increase a study test score by X %
Time Frame: Duration of project
costs and cost effectiveness analysis of the mCME intervention in terms of costs to increase a study test score by X %
Duration of project

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Christopher J Gill, MD MS, Boston University

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.

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

May 1, 2015

Primary Completion (Actual)

November 1, 2015

Study Completion (Actual)

November 1, 2015

Study Registration Dates

First Submitted

March 3, 2015

First Submitted That Met QC Criteria

March 5, 2015

First Posted (Estimate)

March 6, 2015

Study Record Updates

Last Update Posted (Estimate)

January 12, 2016

Last Update Submitted That Met QC Criteria

January 11, 2016

Last Verified

January 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • H-33241

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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