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EMPower: Electronic Media Powering Positive Health Changes in Youth

EMPower: Electronic Media Powering Positive Health Changes in Youth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02444689
Enrollment
91
Registered
2015-05-14
Start date
2015-07-31
Completion date
2020-03-06
Last updated
2020-03-12

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

Conditions

Hypertension, Hypertrophy, Left Ventricular, Obesity, Overweight, Prehypertension

Keywords

Blood pressure, Cardiovascular disease, Children, Adolescent, Pediatrics, End-organ damage

Brief summary

The purpose of this study is to evaluate the effectiveness of a technology-based behavioral Healthy Lifestyle intervention on adiposity (body mass index z-score), blood pressure (mean clinic systolic BP), and heart size (LVM) in comparison to standard care.

Interventions

BEHAVIORALElectronic Media Application

Children in the intervention group will receive motivation, education and coaching regarding therapeutic lifestyle changes via a smart phone electronic media application.

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 22 Years
Healthy volunteers
No

Inclusion criteria

* Overweight or Obese * Speaks English

Exclusion criteria

* No smart phone / smart phone data plan * Not willing to send/ receive text messages or download and use the study applications * Neurological impairment/ developmental delay * New / changes in anti-hypertensive medication or medication known to affect blood pressure within the last 6 months * Prior diagnosis of congenital heart disease or cancer * Pregnancy * Taking medication with weight gain as a side effect * Taking medications for weight loss/ participation in another weight loss program

Design outcomes

Primary

MeasureTime frame
Change in adiposity as measured by change in BMI z-score6 months from date of randomization

Secondary

MeasureTime frame
Change in clinic systolic blood pressure6 months from date of randomization
Change in left ventricular mass index6 months from date of randomization

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026