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The Impact of Using a Smartphone Health Application in the Improvement of Cardiovascular Disease Risk Factors

S

Sultan Qaboos University

Status

Not yet enrolling

Conditions

Hypertension
Hypercholesterolemia
Diabetes Mellitus
Obesity

Treatments

Other: smartphone health application (Opulse)

Study type

Interventional

Funder types

Other

Identifiers

NCT05798442
Opulse app

Details and patient eligibility

About

This study investigates the effectiveness of Mobile health application (mHealth apps) in the improvement of cardiovascular disease risk factors including metabolic and behavioral factors. The app will be tested on patients with any of the modifiable risk factors of CVD such as hypertension, obesity, hyperlipidemia, and impaired glycemic control/type 2 diabetes mellitus .

Full description

The investigators aim in this study to reduce the risk of cardiovascular disease in patients with hypercholesterolemia, diabetes, obesity and hypertension. This will be achieved by motivating healthy lifestyle among the participants such as increasing physical activity and intake of healthy diet and reducing alcohol and tobacco consumption. The tool which will be used to motivate healthy lifestyle is a smartphone application which will be specifically designed to motivate behavioral change. Thus, the investigators hypothesis is that participants who have full access to the mobile application will show improved healthy lifestyle, reduced blood pressure, cholesterol and glucose and reduced BMI compared to the participants who don't have access to the mobile application.

Enrollment

410 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Presentation with at least one of the following metabolic abnormalities:
  • Hypertensions (systolic blood pressure ≥ 130 mmHg and/or diastolic blood pressure ≥ 85 mmHg)
  • Obesity (waist circumference ≥ 80 cm (women) or ≥ 94 cm (men) and BMI ≥ 25 kg/m2)
  • Dyslipidemia (triglycerides ≥ 1.7 mmol/L or/and HDL-cholesterol ≤ 1.29 mmol/L (women) or ≤ 1.02 mmol/L (men) or/and LDL-Cholesterol > 5.18 mmol/L, serum total cholesterol ≥ 5.2 mmol/l)
  • Impaired glycemia/type 2 diabetes (fasting plasma glucose ≥ 5.6 mmol/L)
  • Arabic or English language speaking and able to read and write in one of these languages
  • Possession of a smart mobile phone Willing to utilize a mobile application for CVD management.

Exclusion criteria

  • A history of stroke, myocardial infarction or any related cardiovascular complications Complicated diabetes mellitus e.g., Proliferative diabetic retinopathy, end-stage renal disease
  • Unavailability of a smartphone or any reason that will not allow the participant to use the app properly. (such as; difficulty or inability to use mobile applications, unavailability of network services...etc.).
  • Medical conditions that restrain the participant to be physically active.
  • High chance of loss to follow up at the FAMCO clinic (due to upcoming travel, temporary employment and thus eligibility to be treated at the clinic, irregular visits due to distance from home...etc.)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

410 participants in 2 patient groups

mHealth app-based intervention group
Experimental group
Description:
The app-based intervention group will be given access to a mHealth app that will be specifically designed to motivate the users to increase their physical activity and healthy diet intake while reducing smoking and alcohol intake. The app provides the patients with standardized dietary and exercise guidelines and sends them frequent advice and reminders to follow the guidelines. Changes in the CVD risk factors of the participants will be assessed based on blood biochemical and anthropometric measurements collected every 4 months over a period of 20 months. The app will be designed to include interactive functions which allow the patients to insert their daily caloric intake and exercise, biometric data, track the improvement in their CVD risk factors and CVD risk score.
Treatment:
Other: smartphone health application (Opulse)
face-to-face consultation group
No Intervention group
Description:
This group of patients will not have access to mHealth app and will receive the traditional face to face intervention.

Trial contacts and locations

0

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Central trial contact

Amani Alkhaifi, PhD; Hana Alsumri, PhD

Data sourced from clinicaltrials.gov

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