- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04354168
Nthabi in Lesotho - Implementation
Women's mHealth Program: Nthabi Application in Lesotho
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Lesotho has second-highest HIV and fifth-highest tuberculosis prevalence rates worldwide, and a maternal mortality rate (1024/100,000) that is among the highest in Africa. As there are only 6.2 nurses and 0.5 physicians per 10,000 people, both about one-third of the African average, there is an enormous need for eHealth systems to assist the clinical care system.
Preconception care is an effort to focus on engaging young women in their health before they become pregnant since many women enter pregnancy at risk for poor outcomes because of preexisting medical conditions or not following evidence-based preventive action. In 2013, the WHO prioritized research that focuses on developing, delivering, and scaling preconception women's health interventions in low and middle-income countries to optimize health and birth outcomes. The WHO emphasized implementation research as the key step in helping to maximize the coverage and uptake of preconception care to enhance the long-term health outcomes for women and their children.
The existing "Gabby" system is a patient-facing, user-friendly, evidence-based, scalable, culturally adaptive, health communication system designed to improve women's health. The investigator's team has developed and tested several Embodied Conversational Agents (ECAs), which are virtual characters designed using expertise from health communication, psychotherapy, social psychology, sociolinguistics, linguistics, and communication theory.
For this project, the investigators will first adapt the existing "Gabby" system to a culturally appropriate mHealth application, called "Nthabi", and second, study the impact of the Nthabi application into district hospitals in Lesotho in partnership with the Lesotho Boston Health Alliance (LeBoHA) using the existing educational infrastructure. The research team will assess the effectiveness of Nthabi based on the periodic stage of change assessments over the two-month implementation, end-user content knowledge, and system usage.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Maseru, Lesotho, 105
- Lesotho Boston Health Alliance
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Female Resident of Lesotho
- English Speaking
- Have access to an Android smartphone
- Not currently pregnant at time of enrollment
Exclusion Criteria:
-None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Nthabi mHealth Application
About 20 women from each of the ten district hospitals will be recruited.
Each district hospital will have a separate administrative page on the Nthabi server where women will be enrolled with a unique username and password.
Upon enrollment, the women will be asked to engage with Nthabi for two months to discuss the relevant content areas they are interested in learning more about.
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Nthabi mHealth Application delivers educational content and recommendations to minimize or eliminate health risks.
The content is delivered via the Nthabi application downloaded on an Android phone smartphone.
End-users can select from a list of topics relevant to the Lesotho population to engage with the conversational agent, Nthabi, and discuss conditions such as tuberculosis, HIV testing, healthy diet, and family planning.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Preconception Health Knowledge
Time Frame: Baseline, 4 weeks
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Change in preconception health knowledge will be assessed by a change in the percentage correct scores between the Pre and Post tests which were developed by the investigator.
Higher positive change scores suggest more knowledge about preconception health.
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Baseline, 4 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ease of Use of Nthabi App
Time Frame: 4 weeks
|
This outcome was assessed by responses to a specific question in an investigator developed survey containing 22 questions eliciting responses on a 4-point Likert scale (strongly agree, agree, disagree, and strongly disagree).
The higher the percentage of strongly agree or agree responses the more favorable the results.
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4 weeks
|
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Nthabi App Health Education Content Organized and Timely
Time Frame: 4 weeks
|
This outcome was assessed by responses to a specific question in an investigator developed survey containing 22 questions eliciting responses on a 4-point Likert scale (strongly agree, agree, disagree, and strongly disagree).
The higher the percentage of strongly agree or agree responses the more favorable the results.
|
4 weeks
|
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Able to Complete Tasks Quickly Using Nthabi
Time Frame: 4 weeks
|
This outcome was assessed by responses to a specific question in an investigator developed survey containing 22 questions eliciting responses on a 4-point Likert scale (strongly agree, agree, disagree, and strongly disagree).
The higher the percentage of strongly agree or agree responses the more favorable the results.
|
4 weeks
|
|
Enjoyed Using the Nthabi App
Time Frame: 4 weeks
|
This outcome was assessed by responses to a specific question in an investigator developed survey containing 22 questions eliciting responses on a 4-point Likert scale (strongly agree, agree, disagree, and strongly disagree).
The higher the percentage of strongly agree or agree responses the more favorable the results.
|
4 weeks
|
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Intend to Keep Using the Nthabi App
Time Frame: 4 weeks
|
This outcome was assessed by responses to a specific question in an investigator developed survey containing 22 questions eliciting responses on a 4-point Likert scale (strongly agree, agree, disagree, and strongly disagree).
The higher the percentage of strongly agree or agree responses the more favorable the results.
|
4 weeks
|
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The Nthabi App Was Culturally Appropriate
Time Frame: 4 weeks
|
This outcome was assessed by responses to a specific question in an investigator developed survey containing 22 questions eliciting responses on a 4-point Likert scale (strongly agree, agree, disagree, and strongly disagree).
The higher the percentage of strongly agree or agree responses the more favorable the results.
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Brian Jack, MD, Boston University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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