Skip to main content
Clinical Trials/NCT06473168
NCT06473168
Not yet recruiting
Not Applicable

Walking-related Mobility Assessment in Older People With Multimorbidity

Northumbria University0 sites55 target enrollmentDecember 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Arthritis
Sponsor
Northumbria University
Enrollment
55
Primary Endpoint
Cadence
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

Multimorbidity (the presence of two or more coexisting long-term conditions) is a significant challenge facing the NHS, especially given UK's ageing population and the association with high levels of illness burden and healthcare costs. Over 50% of adults >65 years have multiple long-term conditions (MLTCs).

Our group has validated a broad range of algorithms applied to single wearable sensors that have the potential to capture walking-related mobility outcomes (such as walking cadence and walking speed) accurately and reliably during activities of daily living across five single long-term conditions. These algorithms, however, cannot be readily applied to people with MLTCs because the effect of multimorbidity on mobility is amplified compared to single long-term conditions secondary to a greater number of complications and sequelae. Accordingly, the aim of this study is to validate algorithms that would allow robust estimation of walking-related mobility outcomes during daily life activities in MLTCs.

To meet our objectives, the investigators will perform: i) laboratory-based technical validation of existing and newly developed algorithms for walking-related mobility outcome detection; ii) unsupervised real-life validation of selected algorithms; and iii) examination of how well the validated walking-related mobility outcomes reflect global and disease specific characteristics in older adults with multimorbidity. The investigators will adopt an integrated patient-centric approach where patients with MLTCs will be engaged early in the project to provide input of their perception and concerns regarding mobility limitation in daily life activities.

The investigators aim to recruit 55 older adults (>65 years), men and women, with multiple long-term conditions with the following inclusion criteria: having two or more of the following conditions including osteoarthritis, rheumatoid arthritis, osteoporosis, type 2 diabetes, depression and/or anxiety, hypertension, coronary heart disease, heart failure, atrial fibrillation, chronic obstructive pulmonary disease, asthma, bronchiectasis, chronic kidney disease, cancer, or stroke within the last 5 years.

Registry
clinicaltrials.gov
Start Date
December 1, 2024
End Date
December 31, 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ioannis Vogiatzis

Professor of Rehabilitation Sciences

Northumbria University

Eligibility Criteria

Inclusion Criteria

  • Adults ≥65 years old
  • Able and willing to provide informed consent
  • Able to read and write in English
  • To be mobile (including the use of walking aids)
  • Two or more of the following long terms conditions: Arthritis, Asthma, Atrial fibrillation, Bronchiectasis, Cancer, Chronic kidney disease, Chronic obstructive pulmonary disease, Coronary heart disease, Anxiety, Depression, Diabetes mellitus, Heart failure, Hypertension, Osteoporosis, Parkinson's disease, Peripheral vascular disease, Stroke or transient ischaemic attack

Exclusion Criteria

  • Unable to give consent for the study
  • Severe mental health problems
  • Active malignancy (on chemotherapy/radiotherapy/planned urgent surgery)

Outcomes

Primary Outcomes

Cadence

Time Frame: 7-day real world assessment

Walking cadence measured in the real world obtained from the Inertial Measurement Units placed on the lower back and the wrist measured in steps/minute.

Stride length

Time Frame: 7-day real world assessment

Stride length measured in the real world obtained from the Inertial Measurement Units placed on the lower back and the wrist measured in meters.

Walking speed

Time Frame: 7-day real world assessment

Walking speed measured in the real world obtained from the Inertial Measurement Units placed on the lower back and the wrist measured in m/s.

Stride duration

Time Frame: 7-day real world assessment

Stride duration measured in the real world obtained from the Inertial Measurement Units placed on the lower back and the wrist measured in sec.

Secondary Outcomes

  • Daily steps(7-day real world assessment)
  • Turning angle(7-day real world assessment)
  • Sedentarism(7-day real world assessment)

Similar Trials