Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04506931
Other study ID # 00007318 - xyz
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 15, 2021
Est. completion date April 30, 2021

Study information

Verified date April 2022
Source Johns Hopkins Bloomberg School of Public Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of the study is to adapt and assess the feasibility, quality, and validity of short message service or 'text message' (SMS), interactive voice response (IVR), and computer assisted telephone interviews (CATI) for collecting information on noncommunicable disease (NCD) risk factors


Description:

Using random digit dialing (RDD) sampling technique, RDD participants will be randomized to one of the three arms: 1) SMS or 2) IVR or 3) CATI. Participants in the first study arm will receive an SMS survey. Participants in the second study arm will receive a IVR survey. Participants in the third study arm will receive a CATI survey. The IVR, SMS and CATI questionnaires contain a set of demographic questions and one NCD module (alcohol, or tobacco, or diet, or physical activity, or blood pressure and diabetes). The investigators will examine contact, response, refusal and cooperation rates and demographic representativeness by each study arm.


Recruitment information / eligibility

Status Completed
Enrollment 5676
Est. completion date April 30, 2021
Est. primary completion date April 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Access to a mobile phone - Greater or equal to 18 years of age - In Colombia, conversant in the Spanish language Exclusion Criteria: - Less than 18 years of age

Study Design


Related Conditions & MeSH terms


Intervention

Other:
SMS Survey
Participants will receive a SMS survey
IVR Survey
Participants will receive an IVR survey
CATI Survey
Participants will receive a CATI survey

Locations

Country Name City State
Colombia Pontificia Universidad Javeriana Bogotá

Sponsors (2)

Lead Sponsor Collaborator
Johns Hopkins Bloomberg School of Public Health Pontificia Universidad Javeriana

Country where clinical trial is conducted

Colombia, 

References & Publications (4)

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. — View 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. — View 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. Review. — View 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. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary 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. Through study completion, an average of one month
Primary 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 Through study completion, an average of one month
Secondary 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 Through study completion, an average of one month
Secondary 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 Through study completion, an average of one month
See also
  Status Clinical Trial Phase
Recruiting NCT04105491 - Patient's Expectations, Preferences, Experiences Before, During and After the Treatment With Invisalign® Aligners
Completed NCT03685227 - A Closer Look at Yoga Nidra: Sleep Lab Analyses N/A
Recruiting NCT06397495 - Comparison of Learning Models in Physical Therapy Education N/A
Completed NCT04169646 - Prevention and Intervention of Neck Pain in Swiss Office-Workers N/A
Completed NCT04506918 - Comparison of SMS and IVR Surveys in Tanzania N/A
Recruiting NCT06410014 - Assessment of Overall Functioning in Patients With Complex Health Issues
Completed NCT04832711 - A Community Study of the Risk for Obstructive Sleep Apnea and Respiratory Inflammation in an Adult Chinese Population
Active, not recruiting NCT03805490 - Translation, Cross Cultural Adaptation and Validation of the Italian Version of the Forgotten Joint Score in Total Knee Arthroplasty
Recruiting NCT03335644 - The NutriNet-Santé Study
Completed NCT03772431 - Use of Narrative Voice and Introduction Content to Improve Interactive Voice Response Surveys in Bangladesh and Uganda N/A
Completed NCT03768323 - Airtime Incentive Amounts to Improve Interactive Voice Response Surveys in Bangladesh and Uganda N/A
Completed NCT03773146 - Use of Airtime Structure to Improve Interactive Voice Response Surveys in Bangladesh and Uganda N/A
Completed NCT04513236 - Use of Airtime Timing to Improve Interactive Voice Response Surveys in Bangladesh and Uganda N/A
Completed NCT02865525 - Development and Validation of a Self-administered QUestionnaire to Identify Levers of Adhesion Behavior to Patient's Medication in Order to Adapt the Educational Monitoring.
Terminated NCT02708303 - Mayo Clinic Foregut Surgery Report Card Questionnaire
Completed NCT03772509 - Use of Introduction Mode to Improve Interactive Voice Response Surveys in Bangladesh and Tanzania N/A
Completed NCT03162835 - Development and Clinimetric Properties of the Dutch Pediatric Neurophysiology of Pain Questionnaire in Healthy Children
Completed NCT04684316 - Economic Evaluation of Periodic Occupational Health Screening N/A
Completed NCT04417556 - Validation of Various Sleep Assessment Tools in SICU N/A
Completed NCT03462134 - Predicting the Outcome After Treatment of Meniscal Tears