Comparison of SMS and IVR Surveys in Tanzania
Primary Purpose
Surveys and Questionnaires, Noncommunicable Diseases
Status
Completed
Phase
Not Applicable
Locations
Tanzania
Study Type
Interventional
Intervention
IVR survey
SMS survey
Sponsored by
About this trial
This is an interventional other trial for Surveys and Questionnaires focused on measuring mobile phone surveys, interactive voice response, short message service
Eligibility Criteria
Inclusion Criteria:
- Access to a mobile phone
- Greater or equal to 18 years of age
- Conversant in the Swahili language
Exclusion Criteria:
- Less than 18 years of age
Sites / Locations
- Ifakara Health Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
IVR survey
SMS survey
Arm Description
Participants will receive an IVR survey
Participants will receive an SMS survey
Outcomes
Primary Outcome Measures
Cooperation Rate #1
As defined by American Association for Public Opinion Research, cooperation rate is defined as I/(I+P+R) where I is the number of participants with complete interviews, P is the number of participants with partial interviews, and R is the number of participants with refusals and breakoffs.
Response Rate #4
As defined by American Association for Public Opinion Research, response rate is defined as (I+P)/(I+P+R+eU) where I is the number of participants with complete interviews, P is the number of participants with partial interviews, R is the number of participants with refusals and breakoffs, and eU is the estimated eligible proportion of unknowns
Secondary Outcome Measures
Refusal Rate #2
As defined by American Association for Public Opinion Research, refusal rate is defined as (R)/(I+P+R+eU) where R is the number of participants with refusals and breakoffs, I is the number of participants with complete interviews, P is the number of participants with partial interviews, and eU is the estimated eligible proportion of unknowns
Contact Rate #2
As defined by American Association for Public Opinion Research, contact rate is defined as (I+P+R)/(I+P+R+eU) where I is the number of participants with complete interviews, P is the number of participants with partial interviews, R is the number of participants with refusals and breakoffs, and eU is the estimated eligible proportion of unknowns
Full Information
NCT ID
NCT04506918
First Posted
August 7, 2020
Last Updated
April 25, 2022
Sponsor
Johns Hopkins Bloomberg School of Public Health
Collaborators
Ifakara Health Institute
1. Study Identification
Unique Protocol Identification Number
NCT04506918
Brief Title
Comparison of SMS and IVR Surveys in Tanzania
Official Title
Comparison of Short Message Service (SMS) and Interactive Voice Response (IVR) Mobile Phone Surveys for Non-communicable Disease Risk Factor Surveillance in Tanzania
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
October 23, 2020 (Actual)
Primary Completion Date
April 30, 2021 (Actual)
Study Completion Date
April 30, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins Bloomberg School of Public Health
Collaborators
Ifakara Health Institute
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study focuses on mechanisms to adapt the performance of interactive voice response (IVR) and short message service (SMS) surveys conducted in low-and middle-income (LMIC) setting (Tanzania) and evaluates how the two survey modalities (IVR and SMS) affect survey metrics, including response, completion and attrition rates.
Detailed Description
Using random digit dialing (RDD) sampling technique, participants will be randomized to one of two arms : 1) IVR or 2) SMS. Participants in the first study arm will receive an IVR survey. Participants in the second study arm will receive a SMS survey. The IVR and SMS questionnaires contain a set of demographic questions and one non-communicable disease (NCD) module (alcohol, or tobacco, or diet, or physical activity, or blood pressure and diabetes). We will examine contact, response, refusal and cooperation rates and demographic representativeness by each study arm.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surveys and Questionnaires, Noncommunicable Diseases
Keywords
mobile phone surveys, interactive voice response, short message service
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized to one of two arms : 1) IVR or 2) SMS. Participants in the first study arm will receive an IVR survey. Participants in the second study arm will receive a SMS survey.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
6483 (Actual)
8. Arms, Groups, and Interventions
Arm Title
IVR survey
Arm Type
Experimental
Arm Description
Participants will receive an IVR survey
Arm Title
SMS survey
Arm Type
Experimental
Arm Description
Participants will receive an SMS survey
Intervention Type
Other
Intervention Name(s)
IVR survey
Intervention Description
Participants will receive an IVR survey
Intervention Type
Other
Intervention Name(s)
SMS survey
Intervention Description
Participants will receive a SMS survey
Primary Outcome Measure Information:
Title
Cooperation Rate #1
Description
As defined by American Association for Public Opinion Research, cooperation rate is defined as I/(I+P+R) where I is the number of participants with complete interviews, P is the number of participants with partial interviews, and R is the number of participants with refusals and breakoffs.
Time Frame
Through study completion, an average of one month
Title
Response Rate #4
Description
As defined by American Association for Public Opinion Research, response rate is defined as (I+P)/(I+P+R+eU) where I is the number of participants with complete interviews, P is the number of participants with partial interviews, R is the number of participants with refusals and breakoffs, and eU is the estimated eligible proportion of unknowns
Time Frame
Through study completion, an average of one month
Secondary Outcome Measure Information:
Title
Refusal Rate #2
Description
As defined by American Association for Public Opinion Research, refusal rate is defined as (R)/(I+P+R+eU) where R is the number of participants with refusals and breakoffs, I is the number of participants with complete interviews, P is the number of participants with partial interviews, and eU is the estimated eligible proportion of unknowns
Time Frame
Through study completion, an average of one month
Title
Contact Rate #2
Description
As defined by American Association for Public Opinion Research, contact rate is defined as (I+P+R)/(I+P+R+eU) where I is the number of participants with complete interviews, P is the number of participants with partial interviews, R is the number of participants with refusals and breakoffs, and eU is the estimated eligible proportion of unknowns
Time Frame
Through study completion, an average of one month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Access to a mobile phone
Greater or equal to 18 years of age
Conversant in the Swahili language
Exclusion Criteria:
Less than 18 years of age
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dustin Gibson, PhD
Organizational Affiliation
Johns Hopkins University Bloomberg School of Public Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Honorati Masanja, PhD
Organizational Affiliation
Ifakara Health Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ifakara Health Institute
City
Dar Es Salaam
Country
Tanzania
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
28476729
Citation
Gibson DG, Pariyo GW, Wosu AC, Greenleaf AR, Ali J, Ahmed S, Labrique AB, Islam K, Masanja H, Rutebemberwa E, Hyder AA. Evaluation of Mechanisms to Improve Performance of Mobile Phone Surveys in Low- and Middle-Income Countries: Research Protocol. JMIR Res Protoc. 2017 May 5;6(5):e81. doi: 10.2196/resprot.7534.
Results Reference
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PubMed Identifier
28476725
Citation
Gibson DG, Pereira A, Farrenkopf BA, Labrique AB, Pariyo GW, Hyder AA. Mobile Phone Surveys for Collecting Population-Level Estimates in Low- and Middle-Income Countries: A Literature Review. J Med Internet Res. 2017 May 5;19(5):e139. doi: 10.2196/jmir.7428.
Results Reference
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PubMed Identifier
28476724
Citation
Gibson DG, Farrenkopf BA, Pereira A, Labrique AB, Pariyo GW. The Development of an Interactive Voice Response Survey for Noncommunicable Disease Risk Factor Estimation: Technical Assessment and Cognitive Testing. J Med Internet Res. 2017 May 5;19(5):e112. doi: 10.2196/jmir.7340.
Results Reference
background
PubMed Identifier
28476722
Citation
Hyder AA, Wosu AC, Gibson DG, Labrique AB, Ali J, Pariyo GW. Noncommunicable Disease Risk Factors and Mobile Phones: A Proposed Research Agenda. J Med Internet Res. 2017 May 5;19(5):e133. doi: 10.2196/jmir.7246.
Results Reference
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Comparison of SMS and IVR Surveys in Tanzania
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