NCT03772431

Brief Summary

This study evaluates the effect of two different narrative voices (one male and one female) and two different introductions (one with informational content and the other with additional motivational content) on interactive voice response (IVR) survey cooperation, response, refusal, and contact rates, as compared to a control group (male, informational), in Bangladesh and Uganda.

Trial Health

90
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5,580

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2017

Shorter than P25 for not_applicable

Geographic Reach
2 countries

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 26, 2017

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 17, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 17, 2017

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

December 10, 2018

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 11, 2018

Completed
Last Updated

May 10, 2023

Status Verified

December 1, 2018

Enrollment Period

4 months

First QC Date

December 10, 2018

Last Update Submit

May 9, 2023

Conditions

Keywords

mobile phone surveysinteractive voice responsenarration

Outcome Measures

Primary Outcomes (2)

  • Cooperation rate #1

    As defined by American Association for Public Opinion Research, cooperation rate is defined as I/(I+P+R) where I is complete interviews, P is partial interviews, and R is refusals and breakoffs

    Through study completion, an average of one month

  • 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 complete interviews, P is partial interviews, R is refusals and breakoffs, and eU is the estimated eligible proportion of unknowns.

    Through study completion, an average of one month

Secondary Outcomes (2)

  • Refusal Rate #2

    Through study completion, an average of one month

  • Contact Rate #2

    Through study completion, an average of one month

Study Arms (4)

Male Informational

EXPERIMENTAL

Male voice, informational introduction

Other: Male VoiceOther: Informational Introduction

Male Motivational

EXPERIMENTAL

Male voice, motivational introduction

Other: Motivational IntroductionOther: Male Voice

Female Informational

EXPERIMENTAL

Female voice, informational introduction

Other: Female VoiceOther: Informational Introduction

Female Motivational

EXPERIMENTAL

Female voice, motivational introduction

Other: Female VoiceOther: Motivational Introduction

Interventions

The survey was narrated by a female voice

Female InformationalFemale Motivational

The survey introduction was worded to include motivational content

Female MotivationalMale Motivational

The survey was narrated by a male voice

Male InformationalMale Motivational

The survey introduction was worded to include informational content

Female InformationalMale Informational

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Access to a mobile phone
  • Greater or equal to 18 years of age
  • In Bangladesh, conversant in either English or Bangla language. In Uganda, conversant in either Luo, Luganda, Runyakitara or English languages.

You may not qualify if:

  • Less than 18 years of age

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Institute of Epidemiology Disease Control and Research

Dhaka, Bangladesh

Location

Makerere University School of Public Health

Kampala, Uganda

Location

Related Publications (5)

  • 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.

    PMID: 28476729BACKGROUND
  • 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.

    PMID: 28476725BACKGROUND
  • 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.

    PMID: 28476724BACKGROUND
  • 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.

    PMID: 28476722BACKGROUND
  • Labrique A, Nagarajan M, Kibria GMA, Vecino-Ortiz A, Pariyo GW, Ali J, Kaufman MR, Gibson D. Improving success of non-communicable diseases mobile phone surveys: Results of two randomized trials testing interviewer gender and message valence in Bangladesh and Uganda. PLoS One. 2023 May 24;18(5):e0285155. doi: 10.1371/journal.pone.0285155. eCollection 2023.

MeSH Terms

Conditions

Noncommunicable DiseasesNarration

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and SymptomsCommunicationBehavior

Study Officials

  • Adnan A Hyder, PhD, MBBS

    Johns Hopkins University Bloomberg School of Public Health

    PRINCIPAL INVESTIGATOR
  • George W. Pariyo, PhD

    Johns Hopkins University Bloomberg School of Public Health

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Participants were randomized to one of four narrator/introduction combinations: 1) male voice, informational content; 2) male voice, motivational content; 3) female voice, informational content; 4) female voice, motivational content.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 10, 2018

First Posted

December 11, 2018

Study Start

March 26, 2017

Primary Completion

July 17, 2017

Study Completion

July 17, 2017

Last Updated

May 10, 2023

Record last verified: 2018-12

Data Sharing

IPD Sharing
Will not share

Locations