Last reviewed · How we verify
NCT07255755: REACT
A Double Blind Randomised Clinical Study to Evaluate Attention Improvement in an Adult Population After Cereboost Intake
NA trial testing American Ginseng extract in Attention in 200 participants. Currently enrolling.
1 January 2027
Quick facts
| Lead sponsor | University of East Anglia |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | supportive care |
| Enrollment | 200 |
| Start date | 1 December 2025 |
| Primary completion | 1 January 2027 |
| Estimated completion | 1 January 2027 |
| Sites | 2 locations across United Kingdom |
Drugs / interventions tested
- American Ginseng extract
- Placebo product
Conditions studied
Sponsor
University of East Anglia
Who can join
Adults 18 to 40, any sex, with Attention or Cognition. Healthy volunteers can join.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Measure of Attention
Time frame: Baseline, 2-hours, 4-hours and 6-hours post intervention
Measured by the Attentional Network Task (ANT), expressed by accuracy score (%correct) at 6 hours post consumption
Sponsor's own description
The study will assess the immediate, short-term benefits of a single dose of a supplement containing 200mg of Panax quinquefolius (American Ginseng) on cognition (brain function) in healthy young adults. To understand the effect this product may have, the participants will complete a series of questionnaires and cognitive tests (tests of memory and brain function) at set intervals across a 6-hour period. Blood samples will also be collected to assess the impact of the study product on the participants.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07255755
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Attention
Currently open trials in the same condition.
- NCT07266909 — Impact of Attentional Tunelling on a Population of French Practitioners · recruiting
- NCT07408180 — Exploratory Randomized, Controlled, Dose-response Study on the Impact of Nicotine From Five Variants of a Nicotine Table · NA · active not recruiting
- NCT06837246 — A Clinical Trial to Assess Cognitive Effects of Cognitive Nutritional Supplement in General Population · NA · recruiting
- NCT06587113 — An Investigation of Attentional and Inhibitory Processes During Active Visual Search in Humans · NA · recruiting
- NCT06248268 — Neuropsychological Patterns of Suicide Ideators and Suicide Attempters · recruiting
Other University of East Anglia trials
Trials by the same sponsor.
- NCT07512388 — Acceptance and Commitment Therapy for Post-Stroke Adjustment Via Telerehabilitation · NA · active not recruiting
- NCT06733103 — Pilot of Cognitive Stimulation Therapy for Pre-frail Stroke Survivors · NA · completed
- NCT06971718 — Coronary Bifurcations With Ischaemia and Flow Assessment · recruiting
- NCT05928104 — Optimising Pharmacist-led Medication Reviews in Primary Care · completed
- NCT06451965 — SCED - Wisdom Enhancement for Post-Stroke Depression · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07255755 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of East Anglia
- Last refreshed: 1 December 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07255755.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing