Skip to content

mHealth Intervention to Increase Physical Activity in Prediabetes and Type 2 Diabetes

mHealth Intervention Delivered in General Practice to Increase Physical Activity and Reduce Sedentary Behaviour of Patients With Prediabetes and Type 2 Diabetes

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05351359
Acronym
ENERGISED
Enrollment
343
Registered
2022-04-28
Start date
2022-04-25
Completion date
2025-05-08
Last updated
2026-07-28

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

Conditions

PreDiabetes, Type 2 Diabetes

Brief summary

Sedentary behaviour has a detrimental effect on the mortality, morbidity, and well-being of patients with type 2 diabetes and prediabetes, and general practitioners should advise patients on how to self-monitor and increase their physical activity. The emergence of mobile health (mHealth) technologies unlocks the potential to further improve physical behaviour using an innovative "just-in-time" adaptive approach whereby behavioural support is provided in real-time, based on data from wearable sensors. Thus, the investigators aim to evaluate the effect of a just-in-time mHealth intervention administered by general practitioners on the physical activity and sedentary behaviour of patients with type 2 diabetes and prediabetes. A total of 340 patients will be recruited from 20 general practices across the Czech Republic and randomly assigned to either an active control or intervention group. Both groups will receive brief physical activity advice from their general practitioners and a Fitbit fitness tracker to self-monitor their daily steps, but the intervention group will also receive a mHealth-enabled just-in-time adaptive intervention and regular monthly phone counselling in the first 6 months. The mHealth intervention will be delivered using a custom-developed system (HealthReact) connected to the Fitbit that will trigger just-in-time text messages. For example, a prompt to take a break from sedentary behaviour will be triggered after 30 sedentary minutes or a motivational message with a specific goal to take more steps will be triggered when the total step count is too low. The primary outcome will be the change in daily step count at 6 months, other outcomes include changes in other physical behaviour measures, blood tests, anthropometry and patient-reported outcomes at 6 and 12 months. If the intervention is effective, this study will provide a model of health prevention that can be directly implemented and commissioned within primary care using existing infrastructure.

Interventions

BEHAVIORALmHealth

A mHealth-enabled just-in-time adaptive intervention that is based on the HealthReact system developed by the participating centre at the Faculty of Science of the University of Hradec Kralove. The HealthReact system consists of a server-side application that is connected to the Fitbit server. As such, the system allows for just-in-time text messages triggered by pre-defined context as recorded by the Fitbit wearable monitor. For example, a prompt to take a break from sedentary behaviour can be triggered after 30 sedentary minutes, a suggestion to increase walking cadence can be triggered when continuous, but slow walking is detected, or a motivational message with a specific goal to take more steps to reach their usual daily step count can be triggered when the total daily steps are too low. The mHealth component will be delivered for the entire duration of the study (i.e., 12 months).

BEHAVIORALphone counselling

Regular monthly phone calls by trained counsellors support participants in their effort to increase physical activity and reduce sedentary behaviours. The counsellors will use various behaviour change techniques, such as goal-setting, feedback, action planning, etc. The phone counselling will be provided during the first six months, i.e. 6 phone calls will be delivered.

BEHAVIORALFitbit tracker

Fitbit Inspire 2 will be provided by the general practitioner to study participants at the start of the study to enable objective self-monitoring of physical activity.

BEHAVIORALbrief advice

A brief advice will be provided by the general practitioner at the start of the study.

Sponsors

Charles University, Czech Republic
Lead SponsorOTHER
University of Hradec Kralove
CollaboratorUNKNOWN
St George's, University of London
CollaboratorOTHER
University of Leicester
CollaboratorOTHER
University Ghent
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Diagnosis of prediabetes or T2DM according to the Czech guidelines for GPs on diabetes mellitus1 and prediabetes2, i.e. fasting plasma glucose 5.6-6.9 mmol/l, or 2-h plasma glucose of 7.8-11.0 mmol/l after ingestion of 75 g of oral glucose load for the diagnosis of prediabetes, and fasting plasma glucose ≥ 7.0 mmol/l, or 2-h plasma glucose ≥ 11.1 mmol/l after ingestion of 75 g of the oral glucose load for the diagnosis of T2DM * Age 18 years or older. * Registered at a participating general practice. * Regular users of a smartphone and willing to use it as part of the study. * Written informed consent obtained before any assessment related to the study.

Exclusion criteria

* unable to walk * pregnancy * taking insulin * living in a residential or nursing care home * co-morbid conditions that would affect their adherence to the trial procedures

Design outcomes

Primary

MeasureTime frameDescription
step countfrom baseline to 12-month assessmentchange in daily step count

Secondary

MeasureTime frameDescription
chair-stand testat 6 and 12 monthsfunctional 30s chair-stand test
HbA1cat 6 and 12 monthshaemoglobin A1c
glycemiaat 6 and 12 monthsfasting plasma glucose
lipid profileat 12 monthstotal cholesterol, LDL cholesterol, HDL cholesterol, triacylglycerids
step countat 6 monthschange in daily step count
physical behaviour - average accelerationat 6 and 12 monthsmetric of physical activity volume
physical behaviour - intensity gradientat 6 and 12 monthsmetric of physical activity intensity
sedentary timeat 6 and 12 monthstime per day spent sedentary (in minutes)
sedentary boutsat 6 and 12 monthstime per day (in minutes) spent sedentary in bouts of 30 mins and longer
walking cadenceat 6 and 12 monthscadence (steps/min) in 5 (non-consecutive) highest-cadence minutes
blood pressureat 6 and 12 monthssystolic and diastolic blood pressure
Hospital Anxiety and Depression Scale (HADS)at 6 and 12 monthssymptoms of anxiety and depression: 14 items on a scale 0-3 (a higher score means a worse outcome)
Short Form Survey (SF-12)at 6 and 12 monthsmeasure of health-related quality of life: 12 items using various scales converted to a score 0-100 (a higher score means a better outcome)
body mass indexat 6 and 12 monthsweigh in kilograms divided by height in meters squared

Countries

Czechia

Contacts

STUDY_CHAIRBohumil Seifert, MD, PhD

Charles University, Czech Republic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 29, 2026