Physiological Responses to Upper Limb NMES with Firefly®

  • Research type

    Research Study

  • Full title

    Exploring Local Physiological Changes in the Arm During NMES Using the Firefly® Device

  • IRAS ID

    360302

  • Contact name

    Kieron Day

  • Contact email

    kieron.day@firstkindmedical.com

  • Sponsor organisation

    Firstkind Ltd

  • Duration of Study in the UK

    0 years, 2 months, 1 days

  • Research summary

    This study looks at how a small device called Firefly® affects blood flow and oxygen levels in arm muscles. The Firefly® device sends gentle electrical signals through the skin to stimulate nerves. These nerves then trigger nearby muscles to contract. The device is already approved for treating certain medical issues like swelling (oedema) and helping tendons and ligaments heal. It is also sometimes used more generally for wellness purposes, like increasing circulation after exercise to help with muscle soreness. However, these wellness uses are not part of its official medical approval.

    In this study, we want to see what happens in the arm when the device is used. We will test it on two areas: the upper arm and the forearm. While the device is on, we will check blood flow using ultrasound, which is safe and painless. We will also monitor how much oxygen is in the muscle using a small sensor that sticks to the skin.

    Twelve healthy adults between 18 and 45 years old will take part. Each person will have the device placed on their arm in the two test areas. The device will switch between being on and off several times. The whole visit will take about two hours.

    We don’t expect any problems, but some people may feel a mild tingling, muscle twitching, or slight skin redness where the device or sensors are placed. These effects should go away quickly.

    This study is not a treatment. Instead, it will help us understand how the device affects blood and oxygen flow in the arm. The findings could help with future research on muscle recovery after activity. The study is for information only and does not test the device for any new medical use.

  • REC name

    Wales REC 3

  • REC reference

    25/WA/0223

  • Date of REC Opinion

    23 Jul 2025

  • REC opinion

    Favourable Opinion