Gabby Implementation: Parent Protocol

August 4, 2022 updated by: Boston Medical Center

Implementation of a Health Information Technology System for Young African American Women Into Community-Based Clinical Sites

The Gabby Preconception Care program is an innovative communication system designed to identify and mitigate or resolve health risks for young Black and African American (AA) women before pregnancy, as a means of reducing racial health disparities in birth outcomes. The system uses embodied conversational agent technology the investigators call "Gabby," who empathically interacts with users to assess health risks and delivers interventions to resolve or mitigate these risks. This research team has been working on the "Gabby" Preconception Care program, which features Virtual Patient Advocate (VPA) technology, for over seven years and the system is now ready for dissemination beyond the research environment and into the clinical and community context. The purpose of this project is to examine the implementation and dissemination process of the evidence-based Gabby Program.

Caseworkers at Healthy Start (HS) Programs and healthcare providers at Community Health Centers (CHC's) do not have time to assess for the over 100 preconception health risks that can impact birth outcomes; our system can assist by streamlining that assessment to create a personalized list of risks.Gabby will be introduced/released to sites as part of their standard of care where patients and clients can then share their list with healthcare providers and case workers/managers to make their in-person interactions much more effective. Studies by the research team have shown that Gabby reduces health risks by 25 percent among young Black and AA women. The investigators will evaluate the success of the implementation process through both quantitative and qualitative measures including key informant telephone interviews and guidance from a Gabby Toolkit Advisory Board in order to prepare an implementation toolkit that can be used to facilitate broader dissemination. The Gabby program will not be evaluated as a research intervention, as this has been done previously, instead, how well the Gabby program worked within each site will be assessed.

Study Overview

Detailed Description

The investigators' implementation approach includes: 1) engaging 6 Healthy Starts and 4 CHCs and assessing the workflow and readiness of these clinical sites; 2) implementing the Gabby program for a period of 3-6 months at each of these clinical sites; 3) assembling a preliminary, revised, and final implementation toolkit; and 4) broadly disseminating the toolkit and results of the implementation. Input from a Gabby Toolkit Advisory Board will guide implementation efforts and toolkit development to be used for wider dissemination into other clinical based sites.

Data sources will include qualitative and quantitative methods, such as surveys/ assessments, key informant interviews, system-generated data, learning communities, and implementation logs. Evaluation will focus on site recruitment, training, and engagement; client engagement; clinical risk reduction; toolkit, technical assistance, and support resources; and dissemination efforts.

Study Type

Observational

Enrollment (Actual)

125

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

    • Massachusetts
      • Boston, Massachusetts, United States, 02118
        • Boston Medical Center

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 39 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The study population will consist of staff members at participating sites and clients who use the Gabby system. The staff will be from the 6 selected Healthy Start sites and the 6 selected Community Health Centers who volunteer to participate by responding to a survey, being interviewed, or participating in a focus group about implementation of the Gabby program. The clients will be adult eligible women who receive services from one of the participating sites who meet the eligibility criteria.

Description

Inclusion Criteria:

For staff at Healthy Start sites and Community Health Centers

  • Staff (community health workers, social workers, clinicians, administrators) who work at a participating site
  • Trained about the Gabby system by the investigators
  • Speak and read English

For Gabby system users

  • Women who identify as black or African American who are clients of a participating Healthy Start site or receive care at a participating Community Health Center
  • Currently not pregnant
  • Speaks and read English
  • Has access to a smartphone or laptop/tablet
  • Has internet access
  • Plans to use the Gabby system for 6 months

Exclusion Criteria:

For Staff at Healthy Start sites and Community Health Centers

  • None

For Gabby system users

  • 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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Healthy Start Program 1
Community Partner with HRSA-funded Healthy Start designation and services a patient population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Community Health Center 1
Community Partner with Community Health Center or Federally Qualified Community Health Center designation and services a client population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Healthy Start Program 2
Community Partner with HRSA-funded Healthy Start designation and services a patient population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Community Health Center 2
Community Partner with Community Health Center or Federally Qualified Community Health Center designation and services a client population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Healthy Start Program 3
Community Partner with HRSA-funded Healthy Start designation and services a patient population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Community Health Center 3
Community Partner with Community Health Center or Federally Qualified Community Health Center designation and services a client population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Healthy Start Program 4
Community Partner with HRSA-funded Healthy Start designation and services a patient population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Community Health Center 4
Community Partner with Community Health Center or Federally Qualified Community Health Center designation and services a client population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Healthy Start Program 5
Community Partner with HRSA-funded Healthy Start designation and services a patient population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework
Healthy Start Program 6
Community Partner with HRSA-funded Healthy Start designation and services a patient population with over 50% identifying African American and/or Black
Iimplement an evidence-based preconception care intervention, Gabby, into community-based health settings
Assess implementation outcomes using the Proctor Implementation Outcomes Framework

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Acceptability of Gabby system by staff
Time Frame: 6 months
Information about the acceptability of the Gabby system will be gleaned form qualitative and quantitative data. Virtual interviewers of key staff will be done informed by an interview guide to collect the qualitative data. The quantitative data will be assessed using an investigator developed 33-question Likert scale-based survey. Responses along the 5-point Likert scale will consist of Strongly Disagree (1), Disagree (2), Neutral (3), Agree (4), Strongly Agree (5). Higher score from acceptability related questions indicate greater acceptability.
6 months
Feasibility of Gabby system by staff
Time Frame: 6 months
Information about the feasibility of the Gabby system will be gleaned form qualitative and quantitative data. Virtual interviewers of key staff will be done informed by an interview guide to collect the qualitative data. The quantitative data will be assessed using an investigator developed 33-question Likert scale-based survey. Responses along the 5-point Likert scale will consist of Strongly Disagree (1), Disagree (2), Neutral (3), Agree (4), Strongly Agree (5). Higher score from feasibility related questions indicate greater feasibility.
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total number of preconception health risks for Gabby users
Time Frame: 6 months
The total number of preconception risks is collected during the client/patient's interaction with the Gabby system and will be obtained from Gabby system reports produced by the Gabby System server
6 months
Change in number of preconception risks at 3 months
Time Frame: baseline, 3 months
The number of preconception risks is collected during the client/patient's interaction with the Gabby system and will be obtained from Gabby system reports produced by the Gabby System server
baseline, 3 months
Change in number of preconception risks at 6 months
Time Frame: baseline, 6 months
The number of preconception risks is collected during the client/patient's interaction with the Gabby system and will be obtained from Gabby system reports produced by the Gabby System server
baseline, 6 months
Stage of change for each preconception risk identified
Time Frame: 6 months
The client's stage of change for each preconception risk is collected during the client/patient's interaction with the Gabby system and will be obtained from Gabby system reports produced by the Gabby System server
6 months
Number of Gabby sessions by user
Time Frame: 6 months
The Gabby system records the number of log-ons/sessions for each user which will be obtained from Gabby system reports produced by the Gabby System server.
6 months
Total number of minutes used Gabby
Time Frame: 6 months
The Gabby system records the number of minutes of each session for every user which will be obtained from Gabby system reports produced by the Gabby System server.
6 months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Brian Jack, MD, Boston Medical Center, Family Medicine

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 (Actual)

October 15, 2017

Primary Completion (Actual)

March 15, 2022

Study Completion (Actual)

March 15, 2022

Study Registration Dates

First Submitted

August 12, 2020

First Submitted That Met QC Criteria

August 12, 2020

First Posted (Actual)

August 14, 2020

Study Record Updates

Last Update Posted (Actual)

August 8, 2022

Last Update Submitted That Met QC Criteria

August 4, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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