Heart Surgery's hidden toll: new study tracks mental health before and after cardiac procedures
NCT ID NCT07326384
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how heart procedures change mental health in people with congenital heart disease. About 60 patients will complete surveys on mood, thinking, sleep, and eating before surgery, one month after, and three months after. The goal is to help doctors better screen and support patients' emotional well-being after heart treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with congenital heart disease presenting for palliative or corrective cardiac intervention (surgical or catheter-based).
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
1. Inclusion criteria: * patients of both gender. * Confirmed diagnosis of congenital heart disease requiring surgical or catheter-based intervention. 2. Exclusion criteria: * current or a pre-existing psychiatric or neurological disorder.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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