Improving Congenital Heart Disease Care

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of California, San Francisco

About this trial

The theory-informed digital health intervention, called as "Empower My Congenital Health (EmpowerMyCH)" aims to activate and engage ACHD patients in building confidence toward navigating the adult healthcare system. This tool is built after incorporating the theories of behavior change, gathering inputs from target patients in all stages of its design and implementation. The key features of the tool include a digital medical passport, updated congenital information, community support, and patient stories and advice. The investigators aim to test the acceptability, feasibility, efficacy, and effectiveness of the intervention.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

have congenital heart disease

18 years or older

can sign the informed consent

Disqualifiers

developmentally delayed

unable to consent

Trial design

Design model

Single group

Treatments tested in this trial

  • Digital patient empowerment intervention

    Behavioral

    The intervention has features such as a digital medical passport, updated health-related information, community support and patient/peer stories and advice

Treatment groups

1,000 Participants
are divided into 1 treatment group
Group A: InterventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Recruitment rate

Number of patients recruited out of all the eligible patient approached for recruitment

Time frame
6-12 months
2

Satisfaction with the intervention components

Scores on client satisfaction questionnaire (CSQ-8) survey. Scores are summed across items once. Total scores range from 8 to 32, with the higher number indicating greater satisfaction.

Time frame
0, 6 and 12 months
3

Acceptability of the intervention components

Rates of app downloads. The investigators will download app data monthly to evaluate the frequency and duration of the use of various intervention components. The investigators will recruit 10 participants for focused group discussions on acceptability of the app.

Time frame
0, 6 and 12 months
4

Feasibility of the intervention

Ability to download the app or any technical difficulties with the app or its features.

Time frame
0, 6 and 12 months

Secondary outcomes

1

Patient activation measure (PAM)

The Patient Activation Measure® is a 13-item survey that assesses an individual's knowledge, skills and confidence integral to managing one's own health and healthcare. PAM generates a score along an empirical, interval-level scale from 0-100 that correlates to one of four levels of patient activation. PAM Levels 1 and 2 indicate lower patient activation, while PAM Levels 3 and 4 indicate higher patient activation.

Time frame
0, 6, 12 months
2

Gothenburg Empowerment Scale (GES)

Each question is scored on a 5-point Likert scale, with 1 = strongly disagree and 5 = strongly agree. A higher total score indicates a higher level of empowerment. The GES is a validated and reliable measure of patient empowerment in adults with CHD. It can be used to assess empowerment levels over time, to identify areas where empowerment can be improved, and to evaluate the effectiveness of interventions to promote empowerment.

Time frame
0, 6, 12 months
3

Timely specialist visit

Proportion with scheduled or completed ACHD specialist visits.

Time frame
24 - 36 months
4

Euro-Quality of Life

The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state. Higher score indicates worse quality of life

Time frame
0, 6, 12, and 24 months

Other outcomes

Sponsors and contacts

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

University of California, San Francisco

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator