Validity of Measuring Preoperative Fitness Using Seismofit

Last updated: March 4, 2024
Sponsor: Northumbria University
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

Seismofit

Clinical Study ID

NCT05943730
1614
  • Ages 18-100
  • All Genders

Study Summary

Physical fitness levels of people waiting for a planned operation are often measured using an exercise test. This is because fitness levels help doctors make a plan to improve each person's chances of a successful recovery after their planned operation. The exercise test requires skilled staff, expensive equipment, a 1 hour appointment, and the patient to exercise heavily during the test.

Ventriject, a small to medium sized enterprise, have designed a device called Seismofit that estimates fitness levels of people from a measurement taken whilst laying down. It measures the vibrations of the chest wall caused by the beating heart and uses this information with additional information, such as height, weight and sex, to estimate fitness. The measurement takes around 5 minutes to perform, does not require heavy exercise, expensive equipment or skilled staff.

The Seismofit device was shown to be accurate in young fairly fit people. It has not been tested in people who undergo an exercise test before an operation, who are less fit on average compared to the people that the device was originally tested on. It is likely that the calculations used to estimate fitness levels with the Seismofit device will need to be adjusted for people waiting for an operation. There are two parts to this study. The first part aims to estimate up to 50 people's fitness with the Seismofit device and use directly measured fitness from their standard exercise test before their operation to adjust the calculations for estimating fitness. The second part of this study aims to have a further 50 people undergo the Seismofit device measurement and compare the estimated fitness level with the results from the standard exercise test before an operation. This is to see if the Seismofit device is valid at estimating fitness in people awaiting surgery.

Eligibility Criteria

Inclusion

Inclusion:

  • Adults awaiting major or complex elective surgery classified by the NICE NG45 guideline

  • Referred for and capable of performing a maximum effort CPET as part of standard care within their preoperative assessment

  • Able to be fully supine for 5 minutes

Exclusion:

  • Pacemaker, implantable defibrillator, or any other implantable electronic device in situ

  • Permanent Atrial fibrillation, or other persistent arrhythmia (such as, atrial flutter, bigeminy, trigeminy, frequent premature atrial/ventricular complexes, 2nd degree heart block) documented in the patient's medical history

  • Body mass index (BMI) >35 kg.m-2

  • Severe COPD (defined as FEV1 % predicted <50% [GOLD report, 2022])

  • Pectus excavatum or other chest wall deformity

  • Claudication that limits exercise tolerance

  • Unable to perform maximal CPET

  • Refusal to give informed consent

  • Presence of an absolute contraindication to CPET detailed in the POETTS clinical guideline (Levett et al. 2018).

Study Design

Total Participants: 143
Treatment Group(s): 1
Primary Treatment: Seismofit
Phase:
Study Start date:
August 31, 2023
Estimated Completion Date:
August 01, 2024

Connect with a study center

  • South Tees Hospitals NHS Foundation Trust

    Middlesbrough,
    United Kingdom

    Active - Recruiting

  • Sheffield Teaching Hospitals NHS Foundation Trust

    Sheffield,
    United Kingdom

    Active - Recruiting

  • York and Scarborough NHS Foundation Trust

    York,
    United Kingdom

    Active - Recruiting

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