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.
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
Show all 9Show fewer
- 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
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
- - 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.
- - 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.
- - 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.
- - 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
- Medical history,
- Physical examination: anthropometric measurements (body height, body weight, waist circumference, hip circumference) and vital signs (heart/respiratory rate, blood pressure)
- Body composition (lean mass, fatty mass) by air displacement pletysmography
- Energy expenditure by indirect calorimetry
- Peripheral venous blood sampling: hemoglobin, creatinine,Total, HDL, LDL cholesterol, triglycerides, gamma glutamyl transferase, aspartate aminotransferase (AST), alanine aminotransferase (ALT), bilirubin, glucose, insulin, HbA1c
- Skin accumulation of Advanced Glycation End Products (AGEs)
- Peripheral arterial tonometry for endothelium-dependent vasodilatation
- Pulse oxymetry for oxygen saturation
- Exhaled gas sampling
- Psychological , knowledge and nutritional tests
- measures of psychological well being: Life Orientation Test-Revised (LOT-R); General self efficacy scale (GSES)
- measures of anxiety, depression: Beck Anxiety Inventory (BAI); Beck Depression Inventory (BDI-II)
- 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
- 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
- measure of motivation to change: Motivation to change physical activity, physical activity (MAC2-AF R) ; motivation to change , nutrition (MAC2- AL R)
- measures of health literacy: Newest Vital Sign (NVS) Cardio-metabolic risk scores will be calculated to estimate the CM risk profile <!-- -->
- Heart-SCORE
- Fatty-liver-Index (FLI)
- Finnish Type 2 Diabetes Risk Score (FINDRISC)
- 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.
- Conditions
- Cardiovascular Risk Factor
- 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 group | Role | What they receive |
|---|---|---|
| Repeatability and reproducibility study | Experimental | Monitoring of system ("Wize MIrror") measurements with changes in environmental conditions (fasting state, light, temperature) Receives: Other: Wize Mirror |
| Validation study | Experimental | Longitudinal 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.
Plumpness index
a geodetic measure of the roundness of the face as proxy for overweight
Measured: 3 months
Secondary outcomes (15)
Change in Heart Systematic COronary Risk Evaluation (SCORE)
changes in HeartSCORE, an estimate of cardiovascular risk
Measured: 3 months
Change in HOMA-insulin resistance (IR) index
changes in HOMA-insulin resistance (IR) index, an estimate of insulin resistance
Measured: 3 months
Change in Fatty Liver Index
changes in Fatty Liver Index, an estimate of hepatic steatosis
Measured: 3 months
Change in FINDRISC score
changes in FINDRISC, an estimate of the risk of developing type 2 diabetes
Measured: 3 months
Change in % skin autofluorescence by MultiSpectral analysis
Measured: 3 months
Change in % suborbital skin fat content by MultiSpectral analysis
Measured: 3 months
Change in % Thermal reactive skin hyperemia by MultiSpectral analysis
Measured: 3 months
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
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
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
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
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
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
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
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.
- First posted29 Jun 2016 (estimated)
- Study startJul 2016
- Primary completionOct 2016
- Study completionOct 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cardiovascular Risk FactorStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Istituto di Fisiologia Clinica CNR
- Sponsor type
- University, hospital or other
- Collaborators
- Centre de Recherche en Nutrition Humaine Rhone-Alpe
- Responsible party
- Sponsor
- Investigators
- Maria Aurora Morales, MD, Principal investigator, Istiuto di Fisiologia Clinica del CNR Pisa
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
Study at a glance
From the registry record, last updated by the sponsor on 4 Nov 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- SEMEiotic Oriented Technology for Individual's CardiOmetabolic Risk Self- assessmeNt and Self-monitoring
- ClinicalTrials.gov ID
- NCT02818504
- Acronym / sponsor ID
- SEMEOTICONS / GA 611516
- Conditions
- Cardiovascular Risk Factor
- Keywords
- obesity, dysglycemia, hypercholesterolemia, lifestyle, smoking, physical activity
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 78 participants (actual)
- Lead sponsor
- Istituto di Fisiologia Clinica CNRUniversity, hospital or other
- Collaborators
- Centre de Recherche en Nutrition Humaine Rhone-Alpe
- Study start
- Jul 2016
- Primary completion
- Oct 2016 (actual)
- Study completion
- Oct 2016 (actual)
- First posted
- 29 Jun 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
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
- - 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.
- - 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.
- - 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.
- - 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
- Medical history,
- Physical examination: anthropometric measurements (body height, body weight, waist circumference, hip circumference) and vital signs (heart/respiratory rate, blood pressure)
- Body composition (lean mass, fatty mass) by air displacement pletysmography
- Energy expenditure by indirect calorimetry
- Peripheral venous blood sampling: hemoglobin, creatinine,Total, HDL, LDL cholesterol, triglycerides, gamma glutamyl transferase, aspartate aminotransferase (AST), alanine aminotransferase (ALT), bilirubin, glucose, insulin, HbA1c
- Skin accumulation of Advanced Glycation End Products (AGEs)
- Peripheral arterial tonometry for endothelium-dependent vasodilatation
- Pulse oxymetry for oxygen saturation
- Exhaled gas sampling
- Psychological , knowledge and nutritional tests
- measures of psychological well being: Life Orientation Test-Revised (LOT-R); General self efficacy scale (GSES)
- measures of anxiety, depression: Beck Anxiety Inventory (BAI); Beck Depression Inventory (BDI-II)
- 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
- 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
- measure of motivation to change: Motivation to change physical activity, physical activity (MAC2-AF R) ; motivation to change , nutrition (MAC2- AL R)
- measures of health literacy: Newest Vital Sign (NVS) Cardio-metabolic risk scores will be calculated to estimate the CM risk profile <!-- -->
- Heart-SCORE
- Fatty-liver-Index (FLI)
- Finnish Type 2 Diabetes Risk Score (FINDRISC)
- 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.
Study design
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Repeatability and reproducibility study | Experimental | Other: Wize MirrorMonitoring of system ("Wize MIrror") measurements with changes in environmental conditions (fasting state, light, temperature) |
| Validation study | Experimental | Other: Wize MirrorLongitudinal monitoring of cardiometabolic risk factors through an user---friendly, unobtrusive, personalized system for lifestyle self---management (the "Wize Mirror") |
Who may qualify
- Ages
- 25 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (9 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Wize MirrorInteractive 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 | Other | Repeatability and reproducibility study, Validation study |
Primary outcome
Plumpness index
Time frame: 3 months
a geodetic measure of the roundness of the face as proxy for overweight
15 secondary outcomes
Change in Heart Systematic COronary Risk Evaluation (SCORE)
Time frame: 3 months
Change in HOMA-insulin resistance (IR) index
Time frame: 3 months
Change in Fatty Liver Index
Time frame: 3 months
Change in FINDRISC score
Time frame: 3 months
Change in % skin autofluorescence by MultiSpectral analysis
Time frame: 3 months
Change in % suborbital skin fat content by MultiSpectral analysis
Time frame: 3 months
Change in % Thermal reactive skin hyperemia by MultiSpectral analysis
Time frame: 3 months
Well being index
Time frame: 3 months
Intraclass Correlation Coefficient of % skin autofluorescence by MultiSpectral analysis for light changes
Time frame: Day 15
Intraclass Correlation Coefficient of % skin autofluorescence by MultiSpectral analysis for temperature changes
Time frame: Day 15
Intraclass Correlation Coefficient of % suborbital skin fat content by MultiSpectral analysis for light changes
Time frame: Day 15
Intraclass Correlation Coefficient of % suborbital skin fat content by MultiSpectral analysis for temperature changes
Time frame: Day 15
Intraclass Correlation Coefficient of Thermal reactive skin hyperemia by MultiSpectral analysis for light changes
Time frame: Day 15
Intraclass Correlation Coefficient of Thermal reactive skin hyperemia by MultiSpectral analysis for temperature changes
Time frame: Day 15
Score in the System Usability Scale
Time frame: 3 months (end of study visit)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Nov 2016.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Maria Aurora Morales, MD principal investigator
Istiuto di Fisiologia Clinica del CNR Pisa
3 sites in 2 countries: see every site and its status.
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.