Improving Congenital Heart Disease Care
Recruiting
N/A
Interventional Study
Congenital Heart Disease
Behavior, Health
Quality of Life
Empowerment, Patient
Activation, Patient
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 1,000 (estimated)
- Sponsor
- University of California, San Francisco · Other
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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 to…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* have congenital heart disease
* 18 years or older
* can sign the informed consent
Exclusion Criteria:
* developmentally delayed
* unable to consent
Contacts