Can a daily supplement calm your mind and heart?
NCT ID NCT07502807
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a supplement called Neurofast® can help people who have both anxiety and heart problems. 80 adults aged 18-70 will take the supplement or no extra treatment for 12 weeks. Researchers will measure changes in anxiety, heart rate, and blood pressure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Neurofast® (a dietary supplement)
- What this could lead to
- If it works, this could point toward a simple supplement to help ease anxiety and improve heart health in people with both conditions.
- What could go wrong
- This is a small, early-stage study with no placebo control, so results may be weak or not apply to everyone. Supplements can have side effects or interact with other medications.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
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.
- Ages
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18 to 70 years
- 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.
Inclusion Criteria: * Age 18-70 years (both sexes) * GAD-7 ≥ 5 and/or elevated CAQ score * PHQ-9 \< 20 * Stable clinical status (either no cardiovascular disease or stable cardiovascular disease) * Ability to provide informed consent Exclusion Criteria: * Severe chronic kidney disease (eGFR \< 50 ml/min) * Severe hepatic impairment * Psychotic disorders, bipolar disorder, or acute major depression * Unstable psychiatric or pharmacological treatment (\<3 months) * Pregnancy or breastfeeding * Known allergy or intolerance to investigational treatments (if applicable)
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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 places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names. We don't republish those.
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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.
Contacts and locations
Locations
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University of Rome Tor Vergata
Roma, 00133, Italy
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