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Cardiovascular Risk FactorSEMEOTICONSNCT02818504

SEMEiotic Oriented Technology for Individual's CardiOmetabolic Risk Self- assessmeNt and Self-monitoring

A study testing Wize Mirror in people with Cardiovascular Risk Factor, run by Istituto di Fisiologia Clinica CNR at 3 sites in 2 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Cardio-metabolic risk factors include obesity, physical inactivity, smoke, alcohol abuse, high blood lipids or sugar and arterial hypertension. Systems for self-learning and self-monitoring may help people improve and maintain a healthy lifestyle through tailored suggestions about diet, weight control, physical… Read more about this study

Who is it for?
Ages 25 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Cardiovascular Risk Factor
What is being tested?
Wize Mirror
Could I receive a placebo?
No, everyone receives an active treatment
How many people
78 participants
Where
3 sitesin 2 countries
Study dates
Jul 2016to Oct 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Blood pressure and heart rate measure after 10 minutes lying without treatment: 95 mmHg<Systolic Blood Pressure<160 mmHg; 45 mmHg<Diastolic Blood Pressure<90 mmHg; 40 bpm<Heart rate<100bpm.
  • Broad range of CM risk profile
  • Undergoing medical examination at the inclusion visit
  • Interested and willing to change their lifestyle by decreasing body weight and/or increasing physical fitness and/or improving their well-being following medical advice

Who cannot join

  • History of overt disease, including hypertension, diabetes, dyslipidemia requiring drug treatment
  • Clinical or laboratory findings (lipid, glucose,liver and kidney profile, hemoglobin) at the inclusion visit suggesting any pathological condition requiring treatment
  • Chronic medical treatment other than contraception
  • Declared pregnancy and breastfeeding
  • Claustrophobia
  • Minor or adult under guardianship
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  • Prisoner
  • Expected poor compliance
  • Subject who has exceeded the maximum foreseen compensation for participation in research protocols

Trial locations and contacts

3 sites in 2 countries.

3 sites in 2 countries

Italy2 sites
  • Istituto di Fisiologia Clinica del CNR UOS Milano

    Milan, Milano, 20162

  • Istituto di Fisiologia Clinica del CNR

    Pisa, 56124

Other trials in Italy

France1 site
  • Centre de Recherche en Nutrition Humaine

    Lyon, 69310

Other trials in France

About this study

Cardio-metabolic risk factors include obesity, physical inactivity, smoke, alcohol abuse, high blood lipids or sugar and arterial hypertension. Systems for self-learning and self-monitoring may help people improve and maintain a healthy lifestyle through tailored suggestions about diet, weight control, physical activity, fatigue,stress.

SEMEOTICONS exploits the human face as an indicator of individual's health status and translates signs obtained from the face using contactless sensors into measures and descriptors to be automatically evaluated by a an interactive smart mirror. This "Wize Mirror" extracts descriptors from videos, images and gas concentration signals and integrates them in a virtual model used to compute and trace the evolution of an individual's wellness index. A health diary enables each individual to evaluate and personally relate his/her lifestyle to his/her well-being. Coaching messages are provided, in relation to the evolution of the wellness index and of each descriptor, to provide useful suggestions on correct lifestyle self-monitoring.

Read more

The purpose of this study is assess the accuracy of the information derived from the Wize Mirror in expressing the health status of the individual.

The reproducibility and repeatability study will evaluate whether measurements are stable over short time spans and whether they are influenced by meals light and temperature conditions.

To verify whether the Wize Mirror is able to detect variations in physical and emotional health status with appropriate lifestyle changes, the validation study will cross-check measurements from the Wize Mirror against reference clinical tests at enrolment and after 3 months of personalized suggestions for healthy behavior.

Reference tests include

  • Physician visit
  • Measurement of blood oxygen content and skin end products of sugar metabolism,body composition, energy expenditure, vascular function
  • Laboratory profile and exhaled gas composition
  • Questionnaires on quality of life and lifestyle (food, sleep, physical activity, smoking, alcohol, stress).

Wize Mirror measures include

  • 3D reconstruction of face images for roundness, color, stress and fatigue
  • Heart and respiratory rate
  • Detection of skin sugar metabolism end-products and of eye lipid deposits
  • Small vessel vasodilating ability with local heating The results will allow to assess whether the Wize Mirror is easy to use and helpful for self-monitoring of cardio-metabolic risk.
Read the detailed description

Cardio--metabolic (CM) risk is a cluster of risk factors indicative of a patient's overall risk for cardiovascular diseases (CVD), the leading cause of morbidity and mortality worldwide and type-2 diabetes. CM risk factors include obesity, physical inactivity, smoke, alcohol abuse, abnormal lipid metabolism, hyper-glycaemia and arterial hypertension.

Educational programs and lifestyle interventions represent effective tools to improve the risk profile but they need time consuming and expensive counselling and supervision of various health professionals . A rational alternative to intensive individual coaching is the use of systems for self-learning and self-monitoring, to help people change and maintain a healthy lifestyle through tailored suggestions about nutrition, weight control, physical activity, fatigue, and stress.

SEMEOTICONS exploits the human face as an indicator of individual's health status and translates signs obtained from the face into measures and descriptors to be automatically evaluated by a computerized application, an interactive smart mirror, which seamlessly integrates contactless sensors, such as 3D optical sensors, a multispectral camera, gas detection sensors, and microphones and a touch-screen interface for user's interactions and output visualization.

This "Wize Mirror" collects data in the form of videos, images and gas concentration signals, and extracts a number of biometric, morphometric, colorimetric, and compositional descriptors that represent individual's facial signs. The integration of such descriptors constitute a virtual model used to compute and trace the evolution of an individual's wellness index. A health diary about this index enables each individual to evaluate and personally relate his/her lifestyle to his/her well-being. Coaching messages are provided, in relation to the evolution of the wellness index and of each descriptor to provide useful suggestions on correct lifestyle self-monitoring.

The purpose of this study is assess the accuracy of the information derived from the Wize Mirror in expressing the health status of an individual.

Arm 1 Reproducibility and repeatability study (to be performed at the French site Lyon only).

The reproducibility and repeatability study will evaluate whether Wize Mirror measurements are influenced by meals, light and temperature conditions in 6 healthy volunteers Data will be acquired during 4 modules corresponding to different use conditions of the mirror

  1. - Changes in the fasting state Under artificial lights and at environment temperature (18-20°C), Wize Mirror measurements will be acquired at baseline in the fasting state and at 30, 60 and 120 minutes after a standardized breakfast during three consecutive days.
  2. - Changes in light conditions Wize Mirror measurements will be performed at baseline under artificial lights and at environment temperature (18-20°C) then at 30' under artificial lights and at environment temperature (18-20°C) for 3 times consecutively during the same morning with 20 minutes interval between acquisitions.
  3. - Changes in temperature conditions Wize Mirror measurements will be performed at baseline under artificial lights and at environment temperature (18-20°C) then at 30' under artificial lights and at temperature increased to 28- 30°C, for 3 times consecutively during the same morning with 20 minutes interval between acquisitions.
  4. - Simultaneous changes in light and temperature conditions Wize Mirror measurements will be performed at baseline under artificial lights and at environment temperature (18-20°C) then at 30' under natural lights and at temperature increased to 28- 30°C, in 6 volunteers for 3 times consecutively during the same morning with 20 minutes interval between acquisitions. The visit will last approximately 3 hours. A breakfast will be offered at the end of the visit.

To assess whether measurements are stable over short time spans one of the 6 volunteers will undergo a last visit for the repeatability study in the fasting state. Wize Mirror measurements will be performed at T0 under artificial lights and at environment temperature (18-20°C) for 10 consecutive times with a 30 minutes interval between acquisitions.

During each visit the following Wize Mirror measurements will be performed:

  • face morphometry through 3D reconstruction of face images
  • colorimetric analysis
  • heart rate and respiratory rate
  • autofluorescence detection of protein glycation
  • skin cholesterol content
  • thermal-induced vasodilation by application of warm air at 42°C temperature to the cheek to study microvascular function
  • face expression of stress and fatigue through 3D reconstruction of face images
  • exhaled gas analysis for ethanol and carbon dioxide

Arm 2 Validation study. The validation study will check data measured from the Wize Mirror against reference clinical tests in 60 healthy volunteers. To verify whether the Wize Mirror is able to detect variations in physical and emotional health status with appropriate lifestyle changes, measurements will be cross-checked at enrolment and after 3 months of personalized suggestions for healthy behavior.

Healthy volunteers will undergo at recruitment the following for user profiling for baseline CM risk

  1. Medical history,
  2. Physical examination: anthropometric measurements (body height, body weight, waist circumference, hip circumference) and vital signs (heart/respiratory rate, blood pressure)
  3. Body composition (lean mass, fatty mass) by air displacement pletysmography
  4. Energy expenditure by indirect calorimetry
  5. Peripheral venous blood sampling: hemoglobin, creatinine,Total, HDL, LDL cholesterol, triglycerides, gamma glutamyl transferase, aspartate aminotransferase (AST), alanine aminotransferase (ALT), bilirubin, glucose, insulin, HbA1c
  6. Skin accumulation of Advanced Glycation End Products (AGEs)
  7. Peripheral arterial tonometry for endothelium-dependent vasodilatation
  8. Pulse oxymetry for oxygen saturation
  9. Exhaled gas sampling
  10. Psychological , knowledge and nutritional tests
  11. measures of psychological well being: Life Orientation Test-Revised (LOT-R); General self efficacy scale (GSES)
  12. measures of anxiety, depression: Beck Anxiety Inventory (BAI); Beck Depression Inventory (BDI-II)
  13. measures of quality of life: Perceived Stress Scale (PSS); Short Form (SF)-12 Health Survey; Insomnia Severity Index (ISI) ; World Health Organization (WHO) (Five) Well Being Index
  14. measures of eating and smoking behaviour and physical activity: WHO STEPwise approach to noncommunicable disease risk factor surveillance (STEPS); Audit C Alcohol ; Fagenstrom's test; International Physical Activity Questionnaire (IPAQ) physical activity; Dietary Approaches to Stop Hypertension (DASH) dietary regimen
  15. measure of motivation to change: Motivation to change physical activity, physical activity (MAC2-AF R) ; motivation to change , nutrition (MAC2- AL R)
  16. measures of health literacy: Newest Vital Sign (NVS) Cardio-metabolic risk scores will be calculated to estimate the CM risk profile <!-- -->
  17. Heart-SCORE
  18. Fatty-liver-Index (FLI)
  19. Finnish Type 2 Diabetes Risk Score (FINDRISC)
  20. Homeostasis Model Assessment (HOMA) index

Data acquisition to derive computational descriptors for Wize Mirror functioning will include image (still pictures, videos) acquisition in visible light and infrared band before and after thermal stimulation at 42° C and Exhaled gas sampling using the "Wize Sniffer". During each visit the following Wize Mirror measurements will be performed:

  • face morphometry through 3D reconstruction of face images
  • colorimetric analysis
  • heart rate and respiratory rate
  • autofluorescence detection of protein glycation
  • skin cholesterol content
  • thermal-induced vasodilation by application of warm air at 42°C temperature to the cheek to study microvascular function
  • face expression of stress and fatigue through 3D reconstruction of face images
  • exhaled gas analysis for ethanol and carbon dioxide

Healthy volunteers will then undergo periodically (minimum time interval 2 weeks) face image acquisition, exhaled gas sampling and they will fill through the Wize Mirror screen lifestyle questionnaires till week 12 (end of study). At the end of study visit they will repeat baseline assessments and fill in a questionnaire to evaluate Wize Mirror ease of use and acceptability.

The changes in Wize Mirror measurements obtained at baseline and end of study will be correlated with changes in body weight, waist circumference and Fatty liver index. Relationship with quality of life, or other well-being questionnaire SCORE, standard biochemistry and specific tests will be also assessed.

Being tested
Wize Mirror
Keywords
obesity, dysglycemia, hypercholesterolemia, lifestyle, smoking, physical activity
Medical subject headings
Obesity, Hypercholesterolemia, Smoking, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Wize MirrorOther

    Interactive mirror which integrates contactless sensors and a touch screen interface to derive a semeiotic model of the face with reference to cardiometabolic risk in healthy subjects

Study groups in NCT02818504
Study groupRoleWhat they receive
Repeatability and reproducibility studyExperimentalMonitoring of system ("Wize MIrror") measurements with changes in environmental conditions (fasting state, light, temperature)
Receives: Other: Wize Mirror
Validation studyExperimentalLongitudinal monitoring of cardiometabolic risk factors through an user---friendly, unobtrusive, personalized system for lifestyle self---management (the "Wize Mirror")
Receives: Other: Wize Mirror

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Plumpness index

    a geodetic measure of the roundness of the face as proxy for overweight

    Measured: 3 months

Secondary outcomes (15)
  1. Change in Heart Systematic COronary Risk Evaluation (SCORE)

    changes in HeartSCORE, an estimate of cardiovascular risk

    Measured: 3 months

  2. Change in HOMA-insulin resistance (IR) index

    changes in HOMA-insulin resistance (IR) index, an estimate of insulin resistance

    Measured: 3 months

  3. Change in Fatty Liver Index

    changes in Fatty Liver Index, an estimate of hepatic steatosis

    Measured: 3 months

  4. Change in FINDRISC score

    changes in FINDRISC, an estimate of the risk of developing type 2 diabetes

    Measured: 3 months

  5. Change in % skin autofluorescence by MultiSpectral analysis

    Measured: 3 months

  6. Change in % suborbital skin fat content by MultiSpectral analysis

    Measured: 3 months

  7. Change in % Thermal reactive skin hyperemia by MultiSpectral analysis

    Measured: 3 months

  8. Well being index

    Computation of the individual's well-being index from integration of descriptors in the semeiotic model of the face through structural model equations

    Measured: 3 months

  9. Intraclass Correlation Coefficient of % skin autofluorescence by MultiSpectral analysis for light changes

    Evaluation of the reproducibility of the Wize Mirror measurements with natural or artificial light

    Measured: Day 15

  10. Intraclass Correlation Coefficient of % skin autofluorescence by MultiSpectral analysis for temperature changes

    Evaluation of the reproducibility of the Wize Mirror measurements at ambient temperature of 18-20 °C and 28-30 °C

    Measured: Day 15

  11. Intraclass Correlation Coefficient of % suborbital skin fat content by MultiSpectral analysis for light changes

    Evaluation of the reproducibility of the Wize Mirror measurements with natural or artificial light

    Measured: Day 15

  12. Intraclass Correlation Coefficient of % suborbital skin fat content by MultiSpectral analysis for temperature changes

    Evaluation of the reproducibility of the Wize Mirror measurements at ambient temperature of 18-20 °C and 28-30 °C

    Measured: Day 15

  13. Intraclass Correlation Coefficient of Thermal reactive skin hyperemia by MultiSpectral analysis for light changes

    Evaluation of the reproducibility of the Wize Mirror measurements with natural or artificial light

    Measured: Day 15

  14. Intraclass Correlation Coefficient of Thermal reactive skin hyperemia by MultiSpectral analysis for temperature changes

    Evaluation of the reproducibility of the Wize Mirror measurements at ambient temperature of 18-20 °C and 28-30 °C

    Measured: Day 15

  15. Score in the System Usability Scale

    Assessment of Wize Mirror acceptability by the end users

    Measured: 3 months (end of study visit)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jun 2016 (estimated)
  2. Study startJul 2016
  3. Primary completionOct 2016
  4. Study completionOct 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
78 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02818504
Sponsor's protocol ID
GA 611516
Acronym
SEMEOTICONS
Status last verified
Nov 2016
First submitted
9 May 2016
Last updated
4 Nov 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Wize Mirror in people with Cardiovascular Risk Factor, run by Istituto di Fisiologia Clinica CNR at 3 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Nov 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Italy, France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Plumpness index (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Nov 2016.

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