No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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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
Who this trial is looking for
This trial is looking for adults with congenital heart disease who want to improve their ability to manage their healthcare. Participants will use a digital tool to gain confidence and support regarding their condition.
Are You a Good Fit for This Trial?
You may be able to join if
I have congenital heart disease
I am 18 years or older
I can sign the informed consent
You may not be able to join if
I am developmentally delayed
I am unable to consent
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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…
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.
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria:
* have congenital heart disease
* 18 years or older
* can sign the informed consent
Exclusion Criteria:
* developmentally delayed
* unable to consent
Inclusion Criteria:
* have congenital heart disease
* 18 years or older
* can sign the informed consent
Exclusion Criteria:
* developmentally delayed
* unable to consent
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