Skip to content

Assessment of the effects of the Philips HeartHealth Program among population at risk for cardiovascular disease

A Randomized Parallel Design Study to Assess the Effects of the Philips HeartHealth Program in Subjects at Risk for Cardiovascular Disease - HeartHealth

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/03/005624
Enrollment
364
Registered
2015-03-12
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Heart Health program : Heart-Health program running on app combined with activity heart rate monitor, scale and blood pressure monitor . The participants will be using the devices and

Sponsors

Philips Consumer Lifestyle Personal Health solution
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Be motivated to engage in a more active healthy lifestyle; • Have access to internet at home; • Have a sedentary lifestyle; • May have one or more of the following characteristics: o Overweight/obese (BMI >23 kg/m2) o Mild Hypertension ( o Deranged lipid profile (defined as LDL-C >100 mg/dL or HDL-C 150 mg/dL) (either treatment naïve or on stable anti-hypertensive treatment) • Own smart phone (iOS or Android) with BlueToothLowEnergy

Exclusion criteria

Exclusion criteria: •A Prior history of diabetes (Type I or II) ; •Use of blood glucose lowering medication; •Have a physical condition that inhibits an increase in physical activity; •A prior history of cardiovascular disease (defined as: prior MI, PTCA with intervention, CABG); •LDL-C >190 mg/dl •Pregnancy or breast feeding; •History of disordered eating; including bulimia nervosa, anorexia nervosa; •A BMI lower than 18; •A BMI higher than 40 ; •BP >160/100, with or without prior treatment •already participating in another scientific study.

Design outcomes

Primary

MeasureTime frame
â?¢ The first primary objective of this study is to evaluate the effect of the HeartHealth Program on Health score following 12 weeks of intervention. â?¢ The second primary objective of this study is to evaluate the effect of the HeartHealth Program on physical activity following 12 weeks of intervention. â?¢ The third primary objective of this study is to evaluate the effect of the HeartHealth Program on weight following 12 weeks of intervention. Timepoint: 12 weeks of intervention

Secondary

MeasureTime frame
-Compare effect of the Heart Health Program following 12 weeks and 24 weeks of use, compared to no intervention, as measured by Health score; -To evaluate the effect of the Health score calculation components on the overall Health score at 12 weeks and 24 weeks follow-up. -To explore the extent to which other parameters of health and well-being may have an effect of the observed differences in Health score following 12 and 24 weeksTimepoint: 24 weeks of intervention

Countries

India

Contacts

Public ContactDr RR Kasliwal

Medanta - The Medicity

rr.kasliwal@medanta.org

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026