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Evaluation of a mHealth Platform for Diarrheal Disease Decision-support

Primary Purpose

Diarrhea

Status
Completed
Phase
Not Applicable
Locations
Bangladesh
Study Type
Interventional
Intervention
Smartphone-based decision-support
Paper-based decision-support
Pre-Assessment of practices
Sponsored by
University of Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diarrhea

Eligibility Criteria

2 Months - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Acute uncomplicated diarrhea (less than 7 days with at least 3 loose stools in the last 24 hours)
  • Age greater than or equal to two months.

Exclusion Criteria:

  • No diarrhea
  • Complicated diarrheal disease (e.g. e.g. sepsis, meningitis, convulsions, electrolyte imbalance, myocardial infarction, respiratory failure, chronic kidney disease, severe malnutrition by clinical measures and mid-upper arm circumference (<11.5cm for >= 6 mo to less than 5 years; <11.0 cm for >= 2mo to <6 mo))

Sites / Locations

  • International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Paper-based decision-support

Smartphone-based decision-support

Arm Description

Prior to starting the study, 10 hospitals will be made into 5 pairs. The paper versus smartphone intervention will be randomized to one member of each pair. The study arm will consist of a pre-interventional (6 weeks) followed by an interventional period (12 weeks); this arms will use paper-based decision support at the 5 hospitals designated.

Prior to starting the study, 10 hospitals will be made into 5 pairs. The paper versus smartphone intervention will be randomized to one member of each pair. The study arm will consist of a pre-interventional (6 weeks) followed by an interventional period (12 weeks); this arms will use smartphon-based decision support at the 5 hospitals designated.

Outcomes

Primary Outcome Measures

Use of IV fluid
The percentage of patients prescribed IV fluid between the paper-based decision-support and the Smartphone decision-support.

Secondary Outcome Measures

Use of zinc
The percentage of patients under five years prescribed zinc between the paper-based decision-support and the Smartphone decision-support.
Use of indicated antibiotics
The percentage of patients prescribed the indicated antibiotic over 2 years of age that have acute watery diarrhea and severe dehydration between the paper-based decision-support and the Smartphone decision-support.

Full Information

First Posted
May 12, 2017
Last Updated
October 1, 2019
Sponsor
University of Florida
Collaborators
International Centre for Diarrhoeal Disease Research, Bangladesh, National Institutes of Health (NIH), Fogarty International Center of the National Institute of Health
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1. Study Identification

Unique Protocol Identification Number
NCT03154229
Brief Title
Evaluation of a mHealth Platform for Diarrheal Disease Decision-support
Official Title
The Evaluation of a mHealth Platform for Diarrheal Disease Decision-support in Hospitals: a Cluster Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
March 11, 2018 (Actual)
Primary Completion Date
September 23, 2018 (Actual)
Study Completion Date
September 23, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Florida
Collaborators
International Centre for Diarrhoeal Disease Research, Bangladesh, National Institutes of Health (NIH), Fogarty International Center of the National Institute of Health

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The study hypothesis is that clinical decision-support on a smartphone for the management of diarrheal disease will improve the assessment of dehydration, reduce IV fluid usage, and increase guideline adherence for the use of zinc and antibiotics. To test this hypothesis we will conduct a cluster randomized controlled trial in the diarrhea wards of 10 hospitals in Bangladesh. A 6-week pre-intervention period will establish a baseline at all sites, and in the intervention, hospitals will be randomized to use a paper versus smartphone adaptation of the WHO guidelines by the admitting physician. Inclusion criteria are patients 2 months and older that have uncomplicated acute diarrheal disease; estimated enrollment is 7893 patients. The primary outcome measure is use of IV fluids. This project may have broad impact that will include opportunities to provide improved decision-support for the assessment of dehydration, decreased use intravenous fluids and more prudent use of antibiotics.
Detailed Description
Technology is making possible new approaches to overcome old public health challenges. Cellular networks are now ubiquitous in resource-poor settings and offer new opportunities for high-yield interventions for both chronic and acute diseases. We are specifically interested in developing mHealth solutions for diarrheal disease for two reasons. The first reason is that diarrheal disease globally remains the second leading cause of death for children less than 5 years of age. Barriers to combat this problem include poor adherence to guidelines for rehydrating children and outbreaks often outpace current epidemiological tools. The second reason is that diarrheal diseases in a setting like Bangladesh, including cholera outbreaks, are a model system to develop and test mHealth solutions that can be adapted to more complex chronic and acute diseases in Bangladesh and globally. In partnership with the International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b; primary collaborator) and the Institute of Epidemiology, Disease Control, Research (IEDCR) within the Ministry of Health and Family Welfare in Bangladesh, we propose to compare a paper-based versus a smartphone-based decision-support tool in a cluster randomized controlled trial (cRCT) to determine the impact of the method of decision-support on the use of IV fluids (primary outcome) and indicated medications (secondary outcomes). The smartphone tool is an adaptation of the paper-based World Health Organization guidelines, and is called the 'Rehydration Calculator.' The cRCT will be conducted collaboratively between the icddr,b and government hospitals (N=10) in Bangladesh over 4.5 months per site. A 6-week pre-intervention period will establish a baseline at all sites, and in the intervention, hospitals will be randomized to use the paper versus smartphone tool by the admitting physician. Inclusion criteria are patients 2 months and older that have uncomplicated acute diarrheal disease; estimated enrollment is 7893 patients. Standard of care will be practiced at all sites, with the exception of the decision-support tool(s) in the interventional period. The primary outcome measure is use of IV fluids. This project may have broad impact that will include opportunities to provide improved decision-support for the assessment of dehydration, decrease intravenous fluid use and improve antibiotic stewardship.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster randomized controlled trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
4975 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Paper-based decision-support
Arm Type
Active Comparator
Arm Description
Prior to starting the study, 10 hospitals will be made into 5 pairs. The paper versus smartphone intervention will be randomized to one member of each pair. The study arm will consist of a pre-interventional (6 weeks) followed by an interventional period (12 weeks); this arms will use paper-based decision support at the 5 hospitals designated.
Arm Title
Smartphone-based decision-support
Arm Type
Active Comparator
Arm Description
Prior to starting the study, 10 hospitals will be made into 5 pairs. The paper versus smartphone intervention will be randomized to one member of each pair. The study arm will consist of a pre-interventional (6 weeks) followed by an interventional period (12 weeks); this arms will use smartphon-based decision support at the 5 hospitals designated.
Intervention Type
Other
Intervention Name(s)
Smartphone-based decision-support
Intervention Description
WHO guidelines have been adapted from paper onto a smartphone referred to as a Rehydration Calculator
Intervention Type
Other
Intervention Name(s)
Paper-based decision-support
Intervention Description
WHO guidelines presented on paper
Intervention Type
Other
Intervention Name(s)
Pre-Assessment of practices
Intervention Description
Observation of baseline clinical practice.
Primary Outcome Measure Information:
Title
Use of IV fluid
Description
The percentage of patients prescribed IV fluid between the paper-based decision-support and the Smartphone decision-support.
Time Frame
Intervention is 3 months per hospital
Secondary Outcome Measure Information:
Title
Use of zinc
Description
The percentage of patients under five years prescribed zinc between the paper-based decision-support and the Smartphone decision-support.
Time Frame
Intervention is 3 months per hospital
Title
Use of indicated antibiotics
Description
The percentage of patients prescribed the indicated antibiotic over 2 years of age that have acute watery diarrhea and severe dehydration between the paper-based decision-support and the Smartphone decision-support.
Time Frame
Intervention is 3 months per hospital

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute uncomplicated diarrhea (less than 7 days with at least 3 loose stools in the last 24 hours) Age greater than or equal to two months. Exclusion Criteria: No diarrhea Complicated diarrheal disease (e.g. e.g. sepsis, meningitis, convulsions, electrolyte imbalance, myocardial infarction, respiratory failure, chronic kidney disease, severe malnutrition by clinical measures and mid-upper arm circumference (<11.5cm for >= 6 mo to less than 5 years; <11.0 cm for >= 2mo to <6 mo))
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eric J Nelson, MD PhD
Organizational Affiliation
University of Florida, USA
Official's Role
Principal Investigator
Facility Information:
Facility Name
International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)
City
Dhaka
State/Province
Dhaka Division
ZIP/Postal Code
1212
Country
Bangladesh

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28103233
Citation
Haque F, Ball RL, Khatun S, Ahmed M, Kache S, Chisti MJ, Sarker SA, Maples SD, Pieri D, Vardhan Korrapati T, Sarnquist C, Federspiel N, Rahman MW, Andrews JR, Rahman M, Nelson EJ. Evaluation of a Smartphone Decision-Support Tool for Diarrheal Disease Management in a Resource-Limited Setting. PLoS Negl Trop Dis. 2017 Jan 19;11(1):e0005290. doi: 10.1371/journal.pntd.0005290. eCollection 2017 Jan.
Results Reference
background
PubMed Identifier
33328057
Citation
Khan AI, Mack JA, Salimuzzaman M, Zion MI, Sujon H, Ball RL, Maples S, Rashid MM, Chisti MJ, Sarker SA, Biswas D, Hossin R, Bardosh KL, Begum YA, Ahmed A, Pieri D, Haque F, Rahman M, Levine AC, Qadri F, Flora MS, Gurka MJ, Nelson EJ. Electronic decision support and diarrhoeal disease guideline adherence (mHDM): a cluster randomised controlled trial. Lancet Digit Health. 2020 May;2(5):e250-e258. doi: 10.1016/S2589-7500(20)30062-5.
Results Reference
derived
Links:
URL
http://journals.plos.org/plosntds/article?id=10.1371/journal.pntd.0005290
Description
Pilot study publication

Learn more about this trial

Evaluation of a mHealth Platform for Diarrheal Disease Decision-support

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