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Human augmentation using potassium sensors and the UltraLYNX™ power and communication platform

Human augmentation using a potassium sensor and the UltraLYNX™ power and communication platform for remote interventions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17213693
Enrollment
24
Registered
2025-04-30
Start date
2025-05-16
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy active population Other

Interventions

The study visit component will take place after the safety screening and participants will have arrived at the lab having not consumed caffeine for 24h. During the entire study visit, participants wil
they will be permitted to read during experiments if desired but will otherwise be quiescent to maximise the validity of heart rate variability data. A blood sample will be performed at the start of t

Sponsors

Defence Science and Technology Laboratory
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Any gender 2. 18-40 years old

Exclusion criteria

Exclusion criteria: 1. An intolerance or avoidance of caffeine 2. Any prescribed medication 3. Long term use of ibuprofen (>6 weeks use in the last 52 weeks) 4. Smokers (smoking defined as more than 100 cigarettes throughout the participant’s lifetime) 5. Current vapers defined as any use in the last 7 days 6. Any consumption of liquorice in the last 7 days 7. Self-declared recreational drug use in the last month including, but not limited to, cannabis and cocaine. No drug testing to be conducted. 8. Self-reported alcohol use within the previous 24 hours 9. Any medical condition that could affect safety or study data at the discretion of the Clinical Research Fellow 10. Phobia to needles or anxiety disorders 11. Allergy or sensitivity to materials used in study (e.g., adhesives) 12. Non-English speakers to ensure informed consent 13. Pregnancy – self-tested using a commercial urine test that will be provided 14. Nursing mothers 15. Atrial fibrillation or other clinically significant arrhythmia 16. Any findings that the Clinical Research Fellow believes affect the integrity of study data or the safety to conduct tests 17. Fever 18. Bladder control issues 19. Bleeding disorders 20. Diabetes 21. Irritable Bowel Syndrome (IBS) 22. Epilepsy 23. Glaucoma 24. Osteoporosis 25. Parkinson’s 26. Schizophrenia 27. History of kidney injury

Design outcomes

Primary

MeasureTime frame
Potassium levels measured via a novel potassium sensor at rest via sweat and blood

Secondary

MeasureTime frame
Effect of caffeine administration on physiological response: 1. Electrodermal activity is measured using electrodes on the hand or wrist throughout the 1 hour 30 minute study visit 2. Heart rate variability throughout the 1 hour 30 minute study visit

Countries

England, United Kingdom

Contacts

Public ContactChristopher Gaffney
c.gaffney@lancaster.ac.uk+44 (0) 1524 593602

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026