Enrolling by invitation NCT07285252
Evaluating Non-Invasive Haptics During Extreme Exercise
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Victory Patch with Haptic Vibrotactile Trigger Technology, Sham patch.
- Who it may be relevant to
- Registry conditions: VO2max, Lactate Threshold, Lactate. Basic parameters: 18 years — 85 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United Kingdom
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
ENDURE- Evaluating Non-Invasive Haptics During Extreme Exercise
Overview
This study aims to compare determinants of endurance performance between participants wearing an active patch with haptic vibrotactile trigger technology (VTT) versus a placebo patch without VTT among recreational to competitive runners over a 4-week training period.
Interventions
- Device Victory Patch with Haptic Vibrotactile Trigger Technology
Active Patch with Haptic Vibrotactile Trigger Technology - Device Sham patch
Sham/Placebo Patch without Haptic Vibrotactile Trigger Technology
Primary outcome measures
- Change in VO2 Max [Time frame: 2-weeks and 4-weeks after baseline assessment]
Secondary outcome measures (1)
- Change in Lactate-threshold running speed [Time frame: 2-weeks and 4-weeks after baseline assessment]
Eligibility criteria
Inclusion criteria
- Adults aged 18 years and over, that participate in recreational to competitive distance running (>2 structured runs per week), that were able to complete maximal treadmill exercise safely and were able to attend three laboratory visits were invited to participate.
Exclusion criteria
- Adults with a contraindications to high-intensity treadmill exercise, cardiovascular, metabolic, or musculoskeletal conditions limiting participation, reported use of performance-enhancing drugs, pregnancy, known allergy to adhesives, or current use of neuromodulatory or haptic devices
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Basic science
Study locations
United Kingdom · 1 center
- The Altitude Centre — London
Identifiers
NCT: NCT07285252 · ENDURE-001