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Accelerometery as a measure of modifiable physical activity in high-risk elderly preoperative patients: a prospective observational pilot study
  1. Lisa Grimes1,
  2. Joanne G Outtrim1,
  3. Simon J Griffin2,
  4. Ari Ercole1
  1. 1 University Division of Anaesthesia, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK
  2. 2 Primary Care Unit, University of Cambridge Institute of Public Health, Cambridge, UK
  1. Correspondence to Dr Ari Ercole; ae105{at}cam.ac.uk

Abstract

Objectives To use wrist-worn accelerometers (Axivity AX3) to establish normative physical activity (PA) and acceptability data for the high-risk elderly preoperative population, to assess whether PA could be modified by a prehabilitation intervention as part of routine care, to assess any correlation between accelerometer-measured PA and self-reported PA and to assess the acceptability of wearing wrist-worn accelerometers in this population.

Study design Prospective, observational, pilot study.

Setting Single National Health Service Hospital.

Participants Frail patients≥65 years awaiting major surgery referred to a multidisciplinary preoperative clinic at which they received a routine intervention aimed at improving their PA. 35 patients were recruited. Average age 79.9 years (SD=5.6).

Primary outcomes Normative PA data measured as a mean daily Euclidean norm minus one (ENMO) in milli-gravitational units (mg).

Secondary outcomes Measure PA levels (mg) following a routine preoperative intervention. Determine correlation between patient-reported PA (measured using the Physical Activity Scale for the Elderly) and accelerometer-measured PA (mg). Assess acceptability of wearing a wrist-worn accelerometer measured using Visual Analogue Scale (VAS) questionnaire and device wear time (hours).

Results Median baseline daily PA was 14.3 mg (IQR 9.75–22.04) with an improvement in PA detected following the intervention (median ENMO post intervention 20.91 mg (IQR 14.83–27.53), p=0.022). There was no significant correlation between accelerometer-measured and self-reported PA (baseline ρ=0.162 (p=0.4), post intervention ρ=−0.144 (p=0.5)). We found high acceptability ratings (median score of 10/10 on VAS, IQR 8–10) and wear-time compliance (163.2 hours (IQR 150–167.5) preintervention and 166.1 hours (IQR 162.5–167) post intervention).

Conclusions Accelerometery is acceptable to this population and increases in PA levels measured following an unoptimised routine clinical intervention which indicates that health behavioural change interventions may be successful during the preoperative period. Accelerometers may therefore be a useful tool to design and validate interventions for improving PA in this setting.

Trial registration number NCT03737903.

  • adult anaesthesia
  • surgery
  • elderly
  • perioperative medicine
  • physical activity
  • wearable technology

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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Footnotes

  • Twitter @abitgrim

  • Contributors LG, AE and SJG contributed to the conception and design of the study. LG and JGO contributed to data collection. LG and AE wrote the protocol, were responsible for data analysis and prepared the manuscript. All authors contributed to the review and revision of the manuscript and provided final approval of the version to be published.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval Approval by a Research Ethics Committee was obtained prior to participant recruitment (Research ethics number: 18/SC/0287).

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement The authors will consider reasonable collaborative requests to share data.