Skip to content

Smart Watch Insights for Prevention of Exacerbations and Enhance Rehabilitation - Movement Study

Smart Watch Insights for Prevention of Exacerbations and Enhance Rehabilitation - Movement Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06011356
Acronym
SWIPER-MOVES
Enrollment
1000
Registered
2023-08-25
Start date
2023-08-30
Completion date
2026-08-30
Last updated
2024-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Non-Alcoholic Fatty Liver Disease, Respiratory Disease, Diabetes

Keywords

Digital health, Smart wearable, Population health, Digital biomarkers

Brief summary

Aims of the study: 1. To deliver a scalable wellbeing programme to the local population of Imperial College Healthcare NHS Trust, focusing on movement. 2. To describe the natural history of long-term conditions using digital data from a smartwatch. 3. To identify digital information that is routinely collected by a smart watch that can be used to predict outcomes in patients with long term conditions. 4. To identify factors that determine whether participants engage with and improve in a movement programme. Adult patients who are registered to the Imperial NHS Care Information Exchange (CIE), an NHS patient-facing electronic health record, are eligible to participate in the study. Participants will receive a smart watch for self-monitoring of their movement and wellbeing and be asked to wear the device as much as possible. They will be asked to download a smartphone application called Connected Life, which displays movement and information on heart rate, breathing and oxygen levels to both the participant and the research team (digital data). Participants will receive secure login details for the Connected Life application from the research team, to ensure data privacy. The research team will look at participants' health records, and attempt to identify associations between the digital data and clinical information. This will allow the research team to identify digital data that predicts the onset and natural history of long term conditions, which may potentially allow for earlier diagnosis for future patients. The primary outcome of the study is the identification of trends in movement based on step-count data recorded by the smartwatch.

Interventions

Activity tracker (step count, calories burned), measures heart rate, heart variability and other physiological variables.

Sponsors

Imperial College London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged over 18 years * Registered with the patient-facing electronic health record (Care Information Exchange)

Exclusion criteria

* Unwilling or unable to provide informed consent * Arm or wrist injury or condition prohibiting the safe use of a smartwatch * Any visual impairment preventing the use of the smartwatch or smartphone application.

Design outcomes

Primary

MeasureTime frameDescription
Step count24 monthsChange and trends in step count

Secondary

MeasureTime frameDescription
Quality of life (EQ-5D-5L)24 monthsChange in quality of life as measured by the EQ-5D-5L questionnaire
Patient Activation Measure (PAM)24 monthsChange in patient engagement and confidence over own health, as measured by the Patient Activation Measure

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026