Cardiovascular Disease Clinical Trial
Official title:
A Randomized Controlled Trial of the Effectiveness of a Home-based Interactive E-health Educational Intervention for Middle-aged Cardiovascular Disease Adults in Improving Total Exercise, Adherence Rate, Exercise Efficacy and Outcomes
Cardiovascular disease (CVD) is the leading cause of death globally and e-health educational programs have been proved to be effective support to CVD clients. However, most e-health programs lack personalization and this seldom results in exercise behavioral change. Considering the advantages of e-health programs, as well as the widespread internet use and the rising trend of younger patients having CVD in Hong Kong, we conducted a Randomized Controlled Trial (RCT) to investigate the effectiveness of a home-based interactive e-health educational intervention versus usual care for middle aged cardiac vascular (CV) patients on their total physical exercise, exercise adherence and quality of life.
Introduction:
Cardiovascular disease (CVD) is the leading cause of death globally and e-health educational
programs have been proved to be effective support to CVD clients. However, most e-health
programs lack personalization and this seldom results in exercise behavioral change.
Considering the advantages of e-health programs, as well as the widespread internet use and
the rising trend of younger patients having CVD in Hong Kong, we conducted a Randomized
Controlled Trial (RCT) to investigate the effectiveness of a home-based interactive e-health
educational intervention versus usual care on total physical exercise, exercise adherence
and self efficacy, risk factor profile, psychological outcomes and quality of life for
middle aged cardiac vascular (CV) patients.
Methods and analysis:
This is a prospective randomised clinical trial investigating effectiveness of a home-based
interactive e-health educational intervention for middle-aged cardiovascular disease (CVD)
adults in improving total exercise, adherence rate, exercise efficacy and outcomes. The
hypothesis is that the middle-aged CVD patients (those who are 40-65 years old) would be
more likely to adhere to exercise-based behavior that improves their total exercise,
exercise adherence rate, cardiac risk profile , psychological outcomes and quality of life
with the support of an interactive e-health educational intervention.
The RCT was conducted in two government cardiac clinics in Hong Kong. 438 eligible CV
clients were randomized to either the control group (C) or the intervention group (I) using
block randomization method. All participants received usual care while (I) additionally
received the e-health educational intervention (eHEI) programme. This programme comprised of
one-hour educational session, one telephone follow up and e-health link on self monitoring
including record of health measures and physical exercise across 6 months. Data was
collected at baseline, three months and six months intervals. The primary outcome was total
physical exercise (GSLTPAQ). Secondary outcomes consisted of: exercise efficacy and
adherence rate; CV risk profile; physical and psychological health outcomes (SF12 & HAD);
biological parameter. Data was analyzed using generalized linear models.
Ethics and dissemination: The study complies with the Declaration of Helsinki and was
approved by the University and hospital ethics committee. Study findings will be
disseminated in international conferences and publications.
Key messages:
Cardiovascular disease (CVD) is the leading cause of death globally and most e-health
educational programs have been proved to be effective support to CVD clients. However, most
e-health programs lack personalization and this seldom results in exercise behavioral
change.
The adopted e-health program aims to empower CVD participants by increase knowledge on
cardiovascular risks, perceived benefits of exercise to health, as well as enhance their
self-efficacy in exercise adherence and exercise behavior. Data analysis has been started in
August 2015. This trial will provide evidence of e-health programs on physical and
psychological outcomes comprehensively.
Strengths and limitations of this study:
The study has been designed to meet the criteria for high quality in non-pharmacological
randomised clinical trials with randomisation, multicentre participation, blinded assessment
and analysis with good sample size.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Supportive Care
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