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Effects of Integrated Cardiovascular Health Education Program on Older Adults at Risk of ASCVD

T

The Hong Kong Polytechnic University

Status

Not yet enrolling

Conditions

Healthy Lifestyle
Cardiovascular Diseases
Health Education

Treatments

Behavioral: Usual care
Behavioral: HE programme

Study type

Interventional

Funder types

Other

Identifiers

NCT05434273
ASCVD_OlderAdult_Full

Details and patient eligibility

About

Despite older adults being exposed to an increased risk of atherosclerotic cardiovascular disease (ASCVD), they are generally underrepresented in cardiovascular prevention programmes. The aim of this study is to examine the effects of an integrated exercise and cardiovascular health education programme (HE programme) on community-dwelling older adults at risk of ASCVD.

Full description

The study is a two-arm randomized controlled trial. (1) The control group will mainly receive a basic lifestyle modification talk, a lecture video and governmental education leaflets. (2) The experimental group will receive an integrated exercise and health education programme (HE programme) based on self-efficacy theory. Physical activity level, exercise self-efficacy and ASCVD risk profile including blood pressure, cardiac endurance, fasting blood glucose, fasting blood lipids, and anthropometric outcomes will be investigated via physiological assessments, medical history-taking or questionnaires at baseline, Week 12, Week 24 and Week 36.

Enrollment

190 estimated patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Chinese adults ≧60 years old
  • Having at least one ASCVD risk factor
  • Pass the cardiovascular fitness evaluation
  • Able to write and read Chinese, and communicate in Cantonese;
  • Possess a mobile phone and able to make use of the phone in reading short messages

Exclusion criteria

  • Visually impaired, hearing impaired, or suffer from cognitive, psychiatric, or muscular disorder
  • Having a history of attending similar cardiovascular prevention program
  • Having a previous history of coronary heart disease or stroke

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

190 participants in 2 patient groups

Experimental Arm: Integrated Intervention
Experimental group
Description:
Receive an integrated exercise and cardiovascular health education programme (HE programme)
Treatment:
Behavioral: HE programme
Control
Sham Comparator group
Description:
Receive usual care
Treatment:
Behavioral: Usual care

Trial contacts and locations

1

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Central trial contact

Ka Yan Ho

Data sourced from clinicaltrials.gov

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