Mobility Assessment in Multi-morbidity

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorNorthumbria University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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)

Disqualifiers

Unable to give consent for the study

Severe mental health problems

Active malignancy (on chemotherapy/radiotherapy/planned urgent surgery)

Trial population

Patients will be recruited from outpatient clinics within the Newcastle upon Tyne Hospitals NHS Foundation Trust.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Cadence

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.

Time frame
7-day real world assessment
2

Stride length

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

Time frame
7-day real world assessment
3

Walking speed

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.

Time frame
7-day real world assessment
4

Stride duration

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

Time frame
7-day real world assessment

Secondary outcomes

1

Turning angle

Measured in the real world obtained from the Inertial Measurement Unit placed on the lower back and the wrist expressed in deg/s.

Time frame
7-day real world assessment
2

Daily steps

Measured in the real world obtained from the Inertial Measurement Unit placed on the lower back and the wrist expressed in steps/day.

Time frame
7-day real world assessment
3

Sedentarism

Measured in the real world obtained from the Inertial Measurement Unit placed on the lower back and the wrist indicating time spent in different types of activities such as sitting down, lying, and walking expressed in minutes per day.

Time frame
7-day real world assessment

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Northumbria University

Lead sponsor

Newcastle University

Collaborator

This trial is not recruiting at the moment. You can still explore other options: