Improving Congenital Heart Disease Care for Adolescents and Young Adults
Congenital Heart disease (CHD) is one of the most common birth defects with most major effects diagnosed in infancy. Because there is no cure for CHD it is a lifelong chronic illness. Research is needed to understand the needs of people with CHD as they transition from child to adulthood. This information will improve the care and quality of life for people with CHD.
- All genders
- Over 7 years old
- Volunteers with special conditions
- From Home
Who can participate?
Gender: All genders
Age: Over 7 years old
Volunteers: Volunteers with special conditions
Location: From Home
- Ages 15 and older
- Diagnosed with CHD
- Able to speak, read and write English
- Ability to participate in an interview and complete a survey
- Parent(s) or guardian(s) of participant ages 15-21
- Significant cognitive or visual impairment that prevents participation
- Enrolled and currently participating in another clinical study
- Pregnant or planning to become pregnant during the study
- Moderate to severe respiratory disease
- Moderate to severe heart failure
Will I be paid for my time?