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OpenTrials
Completed

NCT Number: NCT03297866

Effectiveness of Different Incentive Models in Booster up the Second Follow up Response Rate

Aim to test the effectiveness of different incentive models for increasing the follow-up response rate in the current smoker subject.

Completed

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Key information

Age range

15 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Public Opinion Programme, the University of Hong Kong

Hong Kong

About this study

According to the Hong Kong Census and Statistic Department, 10.5% of the Hong Kong population who aged 15 years or above are daily smokers (Thematic Household Survey Report - Report No. 59, 2016). The smoking prevalence was estimated from a thematic household survey that has been conducted every 2 or 3 years. Another population-based survey related to tobacco control is the Tobacco Control Policy-related Survey conducted by the Hong Kong Council on Smoking and Health and the University of Hong Kong. Both surveys were in a cross-sectional design and no follow-up was done. A cohort study with follow-up data could provide more insights for the causal relationship. However, most people are not willing to complete follow-up survey and the response rate is often low (Mellahi, 2016). The low survey response rate could lead to statistically bias in the research funding (Pit, 2014). Therefore, cohort surveys need to provide attractive monetary incentive to the interviewee to increase the response rate (Pit, 2014).

This study aims to assess and compare the 3-month response rate of a follow-up survey due to different financial incentive schemes. The findings will be used for a feasibility assessment of future cohort studies of evaluating tobacco control measures and public opinion, and exploration of appropriate incentive scheme.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 15 or above
  • Cantonese or Mandarin speakers

Exclusion criteria

  • Unable to provide a consent form
  • Speak language other than Cantonese and Mandarin

Treatment and study plan

Primary outcomes

  1. Proportion of respondents who will complete the 3-month follow-up

    Time frame: Finish all telephone survey by Jan 2018

    Proportion of respondents who will complete the 3-month follow-up

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Registry information

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Sep 29, 2017
Registry last updated
May 22, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.