Improving the Heart Health of Home Health Aides

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorWeill Medical College of Cornell University

About this trial

The goal of this early-stage study is to support the heart health of home health aides, a workforce that provides care for adults at home but whose own health has been historically poor. To do this, the study will use Life's Essential 8 (LE8), a program developed by the American Heart Association (AHA) that promotes cardiovascular wellness through education and lifestyle changes. The program has been adapted specifically for home health aides and will be delivered by trained "peer coaches," who are fellow home health aides who will help guide participants through the program.

The main questions the study aims to answer are:

* Will the LE8 intervention, which provides cardiovascular health education and support with positive thinking, be used by home health aides and do they like it? * Does the LE8 intervention actually improve home health aides' cardiovascular health after the intervention's conclusion compared to baseline?

Participants will be paired with a trained peer coach and take part in the 10-week program over the course of 6 months. The program includes support for healthy behaviors and positive thinking, with the goal of making lasting improvements in cardiovascular health.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Currently working as a home health aide

Speak English or Spanish

≥ 18 years of age

Have low CV Health as assessed by LE8 components made up by physical health measurements (blood pressure, BMI) and general self-reported health (physical activity, diet, smoking, sleep); calculated to be a score of 0-50 (the total score ranges from 0-100)

Disqualifiers

Less than 1 year of job experience as a home health aide

Does not possess a smartphone

Gotten dizzy before with a finger stick blood sugar/cholesterol test

Have a history of syncope with a finger stick blood sugar/cholesterol test

Trial design

Design model

Single group

Treatments tested in this trial

  • Peer Coaching Delivered Life's Essential 8 Program

    Behavioral

    This intervention includes structured bi-weekly peer coach (PC) Zoom or telephone sessions and a cardiovascular health curriculum including links to AHA resources. During the 1:1 session, PCs will elicit participants' challenges and successes from the previous week, track progress, and set goals (behavioral targets). PCs will use cognitive training techniques to teach participants how to manage negative thinking and replace it with positive thinking and goal setting. They will be encouraged to work towards these goals and monitor their progress (i.e. getting more physical activity on the job).

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: Peer Coaching Delivered Life's Essential 8 ProgramExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Effectiveness, which will be assessed by a change from baseline in overall cardiovascular health score as measured by LE8.

Each individual Life's Essential 8 (LE8) domain (physical activity level, diet, smoking, sleep, and physiologic health (systolic and diastolic blood pressure), BMI, hemoglobin A1C, and non-HDL cholesterol) has a score of 0 to 100, with higher values indicating better cardiovascular health in each domain. The LE8 overall score is created by averaging individual scores across 8 domains. The overall score ranges from 0 to 100 with higher numerical values corresponding to better cardiovascular health.

Time frame
From baseline to end of the intervention at 6 months

Secondary outcomes

1

Implementation, which will be assessed by acceptability through a qualitative interview

Acceptability defined as participant satisfaction of the study will be assessed through a qualitative interview

Time frame
One 30-90 minute session following the end of the intervention at 6 months
2

Implementation, which will be assessed by acceptability through a survey

Acceptability will be assessed through the 4-item, validated, Acceptability of Intervention Measure. Items are measured on a 5-point Likert scale (Completely Disagree-Completely Agree). The score is calculated as the mean. The scale for this measure ranges from 4-20 with higher scores indicating greater perceived acceptability of the intervention.

Time frame
Following the end of the intervention at 6 months
3

Implementation, which will be assessed by feasibility through a qualitative interview

We will ask peer coaches about the intervention's feasibility, or how viable it was considering their experience, through qualitative interviews.

Time frame
One 30-90 minute session following the end of the intervention at 6 months
4

Implementation assessed by feasibility through HHA eligibility

Feasibility will be assessed with the number of HHAs eligible to receive the intervention.

Time frame
Following the end of the intervention at 6 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Weill Medical College of Cornell University

Lead sponsor

American Heart Association

Collaborator