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Young Adult Hypertension Feasibility Study

myHEART (My Hypertension Education and Reaching Target) Program: a Feasibility Study of a Young Adult Hypertension Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02653573
Acronym
myHEART
Enrollment
9
Registered
2016-01-12
Start date
2015-09-30
Completion date
2016-09-30
Last updated
2016-10-27

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

Conditions

Health Behavior, Hypertension

Keywords

young adult

Brief summary

This study was designed to evaluate the feasibility of a telephone-based health coach self-management intervention for young adults.

Detailed description

To address the unmet need for hypertension care in young adults, MyHEART (My Hypertension Education and Reaching Target), a multi-component hypertension intervention was developed. Eligible patients were identified via the healthcare system's electronic health record. Inclusion criteria included: 1. 18-39 years old at the start of the study, 2. previous hypertension ICD-9 coded office visits and 3. uncontrolled hypertension (≥140/90 mmHg) based on the last ambulatory blood pressure reading. Exclusion criteria included a pre-defined list of co-morbidities, in addition to planned or current pregnancy, any health condition that limits physical activity or dietary changes, current participation in another study, and planning to leave the area in the next three months. During the feasibility study, all participants continued to receive usual hypertension care from their primary care provider. The intervention involved health coach calls over a 3-month period using self-management modules. The order of the modules was guided by the participant's choice. All encounters were documented in the electronic health record. Patient acceptability and home blood pressure monitoring survey data was acquired.

Interventions

BEHAVIORALCoaching

Self-management education

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 39 Years
Healthy volunteers
No

Inclusion criteria

* 18-39 years old at the start of the study * previous hypertension ICD-9 coded office visits * uncontrolled hypertension (≥140/90 mmHg) based on the last ambulatory blood pressure reading

Exclusion criteria

* Chronic Kidney Disease (Stage 4 or 5 or Dialysis) * Congestive Heart Failure, Any Etiology * Activated Healthcare Power of Attorney * Skilled nursing facility or correctional facility residence * Currently enrolled in case management or chronic disease management support services * Sensitive condition diagnosis (e.g. HIV) * Prescribed warfarin, novel oral anticoagulant, or insulin * Diagnosis of sickle cell anemia or cystic fibrosis * Prior stroke, myocardial infarction, coronary artery revascularization * Syncope within past 12 months * Prior or planned organ transplant * Chemotherapy or radiation therapy within 6 months * Severely impaired hearing or speech * Current participation in another research study * Pregnant/planning to become pregnant in the next 12 months * Planning to leave the area in the next 3 months * Any health condition that will limit physical activity or dietary changes * Illegal drug use (other than marijuana) in the past 30 days (Self-report) * Unable to read or communicate in English

Design outcomes

Primary

MeasureTime frameDescription
Patient Satisfaction3 monthsPatient satisfaction survey of feasibility study

Secondary

MeasureTime frameDescription
Out-of-clinic blood pressures3 monthsFrequency of home or out-of-clinic blood pressure monitoring

Outcome results

None listed

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