Use of Airtime Timing to Improve Interactive Voice Response Surveys in Bangladesh and Uganda
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04513236 |
|
Recruitment Status :
Completed
First Posted : August 14, 2020
Last Update Posted : August 14, 2020
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Surveys and Questionnaires Noncommunicable Diseases | Other: Pre-survey incentive Other: Post-survey incentive | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 2287 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Intervention Model Description: | Participants were randomized to one of three airtime incentive timings: 1) no incentive; 2) 0.1X incentive received before the IVR noncommunicable disease risk factor survey is sent, followed by 1X incentive upon completing the survey; or 3) 1X incentive received upon completing the survey. |
| Masking: | Single (Outcomes Assessor) |
| Primary Purpose: | Other |
| Official Title: | A Randomized Controlled Trial of Varying Airtime Incentive Timing to Improve Interactive Voice Response (IVR) Survey Performance in Bangladesh and Uganda |
| Actual Study Start Date : | March 26, 2017 |
| Actual Primary Completion Date : | November 1, 2017 |
| Actual Study Completion Date : | November 1, 2017 |
| Arm | Intervention/treatment |
|---|---|
|
No Intervention: Control
No Airtime Incentive was given for completing the survey
|
|
|
Experimental: Pre-survey incentive
0.1X incentive before the survey, 1X afterwards
|
Other: Pre-survey incentive
An incentive of is given in the form of airtime to motivate participants to complete the survey. Participants were sent 0.1X before the were sent a mobile phone survey and an additional 1X after completing the survey. |
|
Experimental: Post-survey incentive
1X incentive after the survey
|
Other: Post-survey incentive
An incentive in the form of airtime to motivate participants to complete the survey. Participants were given Bangladeshi Taka or Ugandan Shillings worth of certain airtime for completing the survey. |
- Cooperation Rate #1 [ Time Frame: Through study completion, an average of one month ]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.
- Response Rate #4 [ Time Frame: Through study completion, an average of one month ]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
- Refusal Rate #2 [ Time Frame: Through study completion, an average of one month ]As defined by American Association for Public Opinion Research, refusal rate is defined as (R)/(I+P+R+eU) where R is refusals and breakoffs, I is complete interviews, P is partial interviews, and eU is the estimated eligible proportion of unknowns
- Contact Rate #2 [ Time Frame: Through study completion, an average of one month ]As defined by American Association for Public Opinion Research, contact rate is defined as (I+P+R)/(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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- 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.
Exclusion Criteria:
- Less than 18 years of age
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04513236
| Bangladesh | |
| Institute of Epidemiology Disease Control and Research | |
| Dhaka, Bangladesh | |
| Uganda | |
| Makerere University School of Public Health | |
| Kampala, Uganda | |
| Principal Investigator: | 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 |
| Responsible Party: | Johns Hopkins Bloomberg School of Public Health |
| ClinicalTrials.gov Identifier: | NCT04513236 |
| Other Study ID Numbers: |
00007318-4 |
| First Posted: | August 14, 2020 Key Record Dates |
| Last Update Posted: | August 14, 2020 |
| Last Verified: | August 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
mobile phone surveys interactive voice response incentive |
|
Noncommunicable Diseases Disease Attributes Pathologic Processes |

