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N/A N=284 Randomized Prevention

Water, Sanitation, and Hygiene Mobile Health Messages as an Innovative Tool to Facilitate Behavior Change

Cholera

Enrolled (actual)
284
Serious AEs
0.0%
Results posted
May 2024
Primary outcome: Primary: Number of Participants That Reported Handwashing With Soap at Stool and Food Related Events — 37; 4; 27; 10 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
CHoBI7 mHealth program Arm (Behavioral); general message on oral rehydration solution (ORS) (Behavioral)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Johns Hopkins Bloomberg School of Public Health
Primary completion
Nov 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants That Reported Handwashing With Soap at Stool and Food Related Events
37; 4; 27; 10
PRIMARY
Post Intervention Chlorine Concentration in Drinking Water
23; 0
SECONDARY
Percentage of Diarrheal Events
11; 4

Summary

Develop a scalable approach for delivering water, sanitation, and hygiene (WASH) messages to households in areas with confirmed cholera patients in Dhaka, Bangladesh. This will be done by conducting formative research through in-depth interviews, focus group discussions, and intervention planning workshops with households in areas with confirmed cholera patients and government officials to identify perceptions of WASH behaviors and to inform the development of a mobile health intervention (mHealth) for this population. This intervention approach will then be piloted in a subset of households, and revised according to feedback. Then the investigators will conduct a randomized controlled of the refined mHealth intervention.

Eligibility Criteria

Inclusion Criteria

  • At least one household member must report ownership of an active mobile phone in their possession on the day of enrollment

Exclusion Criteria

  • Household has a tap or basin with running water inside their home.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04816552). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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