EMT-OCSP: Effects of Message Framing and Time Discounting on Health Communication for Optimum Cardiovascular Disease and Stroke Prevention

Sponsor
West China Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04450888
Collaborator
Centers for Disease Control and Prevention, China (Other), Beijing Tiantan Hospital (Other), First Affiliated Hospital of Chongqing Medical University (Other), China Stroke Databank Center (Other)
13,114
1
4
18.7
700.3

Study Details

Study Description

Brief Summary

Effects of Message framing and Time discounting on heath communication for Optimum Cardiovascular disease and Stroke Prevention(EMT-OCSP)is a pragmatic, 2 × 2 factorial, randomized, controlled, observer blinded, multicenter trial with four parallel groups. It aims to determine if risk and intervention communication strategy(gain-framed versus loss-frame, long-term context versus short-term context and the potential interaction)have different effect on optimizing adherence to clinical preventive management (in the endpoint of CVD risk reduction)for subjects with at least one moldable risk factor for CVD.

Condition or Disease Intervention/Treatment Phase
  • Other: The strategic use of messages in risk communication
N/A

Detailed Description

Scientific title Effects of Message framing and Time discounting on health communication for Optimum Cardiovascular disease and Stroke Prevention(EMT-OCSP): a pragmatic randomised controlled study

Principal Investigator Li He

Study period 2020-07-01-2022-01-21

Hypotheses and aims When communicating cardiovascular disease(CVD)risk to individuals, different presentation of information carries its own connotations and biases. The one or the other pattern of the presentation may affect individuals' decision making.This study aims to determine if risk and intervention communication strategy(gain-framed versus loss-frame, long-term context versus short-term context and the potential interaction)have different effect on optimizing adherence to clinical preventive management (in the endpoint of CVD risk reduction)for subjects with at least one moldable risk factor for CVD. We aim to provide evidence for practitioners regarding messaging strategies that improve communication effectiveness and further reduce the risk of CVD events in the population, as well as to develop more effective communication strategies for groups of people with different characteristics to maximise patient adherence to lifestyle modifications and medical treatment.

Primary outcome Ten-year CVD risk, lifetime CVD risk and CVD-free life expectancy after 1 year according to the LIFE-CVD model.

Secondary outcomes CVD risk factors [blood pressure(BP) and serum cholesterol, low-density lipoprotein (LDL), non-high-density lipoprotein (HDL), triglycerides and fasting glucose levels],lifestyle factors (physical activity, tobacco use, alcohol use and eating habits), pharmacological treatments for hypertension, dyslipidaemia and diabetes, and anti-thrombotic drug prescriptions after 1 year.

Study design The EMT-OCSP trial is designed as a pragmatic, 2 × 2 factorial, randomized, controlled, observer blinded, multicenter trial with four parallel groups. Randomization will be performed as block randomization with a 1:1:1:1 allocation.

Study population and sample size Subjects with at least one moldable risk factor for CVD. The sample size calculations revealed that the enrolment of 15,000 participants would be sufficient, allowing for a 20% drop-out rate.

Follow-up period One year

Study Design

Study Type:
Interventional
Actual Enrollment :
13114 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effects of Message Framing and Time Discounting on Health Communication for Optimum Cardiovascular Disease and Stroke Prevention(EMT-OCSP): a Pragmatic,Multi-centre, Observer-blinded,12-month Randomised Controlled Study
Actual Study Start Date :
Jul 1, 2020
Actual Primary Completion Date :
Jan 22, 2022
Actual Study Completion Date :
Jan 22, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: Model A

Total cardiovascular disease (CVD)-free life expectancy gain in one's remaining life.

Other: The strategic use of messages in risk communication
The interventions in the EMT-OCSP study are strategic health messages delivered (gain-framed vs.loss-framed and long-term vs.short-term contexts) to individuals based on their calculated CVD-free life expectancy and potential interventional benefits.

Other: Model B

Average CVD-free life expectancy gain per year.

Other: The strategic use of messages in risk communication
The interventions in the EMT-OCSP study are strategic health messages delivered (gain-framed vs.loss-framed and long-term vs.short-term contexts) to individuals based on their calculated CVD-free life expectancy and potential interventional benefits.

Other: Model C

Total CVD-free life expectancy loss that can be reclaimed in one's remaining life.

Other: The strategic use of messages in risk communication
The interventions in the EMT-OCSP study are strategic health messages delivered (gain-framed vs.loss-framed and long-term vs.short-term contexts) to individuals based on their calculated CVD-free life expectancy and potential interventional benefits.

Other: Model D

Average CVD-free life expectancy loss that can be reclaimed per year.

Other: The strategic use of messages in risk communication
The interventions in the EMT-OCSP study are strategic health messages delivered (gain-framed vs.loss-framed and long-term vs.short-term contexts) to individuals based on their calculated CVD-free life expectancy and potential interventional benefits.

Outcome Measures

Primary Outcome Measures

  1. 10-year CVD risk [At the 1-year follow-up]

  2. Lifetime CVD risk [At the 1-year follow-up]

  3. CVD-free life expectancy [At the 1-year follow-up]

Secondary Outcome Measures

  1. Changes in systolic and diastolic blood pressure [At the 1-year follow-up]

  2. Changes in serum cholesterol level [At the 1-year follow-up]

  3. Changes in serum LDL level [At the 1-year follow-up]

  4. Changes in serum non-HDL level [At the 1-year follow-up]

  5. Changes in serum triglycerides level [At the 1-year follow-up]

  6. Changes in fasting glucose level [At the 1-year follow-up]

  7. Changes in physical activity (International Physical Activity Questionnaire or International Physical Activity Questionnaire Short Version Modified for Elderly) [At the 1-year follow-up]

  8. Changes in tobacco use [At the 1-year follow-up]

    Tobacco use status (current, former, never) in the records at visits

  9. Changes in alcohol use (AUDIT questionnaire) [At the 1-year follow-up]

  10. Changes in dietary habits (food frequency questionnaire) [At the 1-year follow-up]

  11. Changes adherence to pharmacological treatments for hypertension (proportion of persistent medication user) [At the 1-year follow-up]

    A persistent medication user is defined as a participant who has purchased the drug at least once during each 3-month interval during our study.

  12. Changes adherence to pharmacological treatments for dyslipidaemia (proportion of persistent medication user) [At the 1-year follow-up]

  13. Changes adherence to pharmacological treatments for diabetes (proportion of persistent medication user) [At the 1-year follow-up]

  14. Changes adherence to anti-thrombotic therapy (proportion of persistent medication user) [At the 1-year follow-up]

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • aged 45-80 years,

  • personally own and use a smartphone (Apple or Android platform) with Internet access,

  • and have at least one of the following CVD risk factors: history of CVD at age < 60 years in a first-degree relative, smoking, diabetes, hypertension, and low-density lipoprotein (LDL)cholesterol ≥ 4.5 mmol/L.

Exclusion Criteria:
  • participants with histories of CVD, heart failure, or chronic kidney disease (estimated glomerular filtration rate < 30 mL/min/1.73m2);

  • those with terminal malignancy at baseline;

  • those with severe psychological or mental disorders

  • violation of the study protocol and participation in another clinical study during follow-up

Contacts and Locations

Locations

Site City State Country Postal Code
1 Health center of Sipo town Yibin Sichuan China

Sponsors and Collaborators

  • West China Hospital
  • Centers for Disease Control and Prevention, China
  • Beijing Tiantan Hospital
  • First Affiliated Hospital of Chongqing Medical University
  • China Stroke Databank Center

Investigators

  • Principal Investigator: Li He, M.D., West China Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Li He, Professor, West China Hospital
ClinicalTrials.gov Identifier:
NCT04450888
Other Study ID Numbers:
  • 610041
First Posted:
Jun 30, 2020
Last Update Posted:
Mar 10, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 10, 2022