ClinicalTrials.gg
Enrolling by invitationNCT07285252ENDUREUpdated Aug 20, 2026

Evaluating Non-Invasive Haptics During Extreme Exercise

An interventional study of Victory Patch with Haptic Vibrotactile Trigger Technology and Sham patch in VO2max, Lactate Threshold and Lactate, sponsored by SuperPatch Limited LLC. Enrolling by invitation at 1 site in United Kingdom. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2026-08-20.

Sponsored by SuperPatch Limited LLC · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Primary completion was expected by Aug 2026, 3 months ago, but the record still lists the study as enrolling by invitation.
  • Registered 10 months after the study started (first participant enrolled Jan 2025, registered Dec 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Non-randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • VO2max
  • Lactate Threshold
  • Lactate

Keywords

  • VO2 max
  • lactate threshold
  • lactate
03

In context

Lead sponsor

SuperPatch Limited LLC is the lead sponsor of 7 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Adults with a 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
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
75 participants (estimated)

Study arms

  • Active comparator
    TREATMENT

    Victory Patch

    Device: Victory Patch with Haptic Vibrotactile Trigger Technology

  • Placebo comparator
    CONTROL

    Sham Comparator

    Device: Sham patch

Interventions

  • DeviceVictory Patch with Haptic Vibrotactile Trigger Technology

    Active Patch with Haptic Vibrotactile Trigger Technology

  • DeviceSham patch

    Sham/Placebo Patch without Haptic Vibrotactile Trigger Technology

06

What researchers measure

Primary outcomes

  1. Change in VO2 Max

    Change in VO₂max (mL/kg-¹/min-¹, calculated as a 30-second rolling average)

    Time frame: 2-weeks and 4-weeks after baseline assessment

Secondary outcomes

  1. Change in Lactate-threshold running speed

    Measurement of Lactate-threshold running speed using capillary sampling (LT, km/h-¹), determined using a DmodMax algorithm on lactate-speed curves \[15\], (2) serum lactate level at threshold (mmol·L-¹).

    Time frame: 2-weeks and 4-weeks after baseline assessment

07

Study locations

1 site
  • The Altitude Centre
    London, UK E1 6AH, United Kingdom
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report

Time frame: Upon Initiation of the Study

Access criteria: Current Study Investigators and associated Research Staff

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07285252
Collaborators
Clarity Science LLC, The Altitude Centre, Vichag Healthcare Research
Responsible party
Sponsor
First posted
Dec 16, 2025
Start date
Jan 5, 2025
Primary completion
Aug 2026 (estimated)
Completion
Sep 2026 (estimated)
Last update
Aug 20, 2026

Study contacts

Mark Sakr, DO
principal investigator · University of Arizona

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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