Effectiveness to Weight Loss in Sedentary and Overweight People Using a Smartphone Application. (EVIDENT3)
Primary Purpose
Healthy
Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Intervention group
Control: Lifestyle counseling
Sponsored by

About this trial
This is an interventional prevention trial for Healthy focused on measuring Physical activity, Food Habits, Information and communiation Technology, Health education
Eligibility Criteria
Inclusion Criteria:
- Obese subjects (IMC ≥ 27.5 to <40), classified as sedentary according to the short physical activity questionnaire validated in the EVIDENT II study.
Exclusion Criteria:
- Older than 65 years are excluded, due to difficulties in the use of ICTs.
- Advanced respiratory, renal or liver disease.
- Several mental illness
- Coronary or cerebrovascular atherosclerotic disease, grade II or higher NYHA heart failure.
- Moderate or severe COPD
- Muscular-skeletal pathology that inhibit mobility
- Subjects who can not exercise or follow a hypocaloric diet.
- Oncologic disease in treatment diagnosed in the last 5 years.
- Terminal situation
- Pregnancy
- Bariatric surgery
- Those with any other circumstance that the investigators consider could interfere with the study procedures
Sites / Locations
- Primary Care Research Unit - The Alamedilla Center for Health
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Control: Lifestyle counseling
Intervention group
Arm Description
Counseling on physical activity and nutrition.
Add for three months a Smartphone with an app (EVIDENT III) and a Smartband to lose weight and improve physical activity.
Outcomes
Primary Outcome Measures
Weight reduction
Measurement by kilograms
Secondary Outcome Measures
Increase steps/day
Steps/day by accelerometer
Decrease sedestation minute week
Minutes week in sedentary activity by Activpal monitor
Decrease total caloric intake/day
Calories/day by Food frecuency questionnaire
Improve Quality of life
Measurement by IWQOL-L
Augmentation index
Central and peripheral augmentation index
Adiponectin
Inflammation marker
Full Information
NCT ID
NCT03175614
First Posted
May 31, 2017
Last Updated
March 1, 2021
Sponsor
Fundacion para la Investigacion y Formacion en Ciencias de la Salud
Collaborators
Instituto de Salud Carlos III
1. Study Identification
Unique Protocol Identification Number
NCT03175614
Brief Title
Effectiveness to Weight Loss in Sedentary and Overweight People Using a Smartphone Application.
Acronym
EVIDENT3
Official Title
EVIDENT3 Study: A Randomized, Controlled Clinical Trial to Reduce Inactivity and Caloric Intake in Sedentary, Overweight People Using a Smartphone Application. Study Protocol.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
June 30, 2020 (Actual)
Study Completion Date
June 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundacion para la Investigacion y Formacion en Ciencias de la Salud
Collaborators
Instituto de Salud Carlos III
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a randomized clinical trial aimed at obese and sedentary subjects aged 20 to 65 years selected in urban primary care centers of 5 centers (Spain). Its objective is to evaluate the effects of the addition of an ICT tool developed for the Smartphone application and a Smartband in support of behavioral and educational recommendations to reduce weight.
Detailed Description
Objetive: To develop and validate an application for the use in Smartphone in which the management of a SmartBand is included and evaluate the effect of adding this tool of information and communication technology (ICT), to a standardized intervention reduce weight, reduce sedestation time, increase physical activity and decrease total caloric intake in obese and sedentary subjects.
Design and setting: A clinical of two parallel group, multicenter, randomized, aimed at assessing the effects of adding an ICT tool (intervention) to support behavioral and educational recommendations (control) in physical activity and weigh loss. Population: 700 obese and sedentary subjects will be included, 20 to 65 aged, selected by random sampling in 5 centers.
Measurements and intervention: physical and sedeentary acivity will be assessed with an accelometer and IPAQ and Marshall Questionnaires, the nutrition by a food frequency and adherence to the Mediterranean diet survey and weight loss with body mass index and waist circumference. Vascular function with a wrist-worn tonometer (blood pressure, augmentation index and pulse rate) will be evaluated and also the Cardio Ankle Vascular Index and carotid intima media thickness. The advice on nutrition (plate method) and exercise will be common to both groups. The intervention group will be added a training for 3 months in use of ICT tool described, designed to foment a healthy and low-calorie diet and increased physical acivity and decreased sedentary.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy
Keywords
Physical activity, Food Habits, Information and communiation Technology, Health education
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
650 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control: Lifestyle counseling
Arm Type
Active Comparator
Arm Description
Counseling on physical activity and nutrition.
Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Add for three months a Smartphone with an app (EVIDENT III) and a Smartband to lose weight and improve physical activity.
Intervention Type
Other
Intervention Name(s)
Intervention group
Intervention Description
Smartphone with APP (EVIDENT III) and a Smartband for 3 months. Counseling on physical activity and nutrition
Intervention Type
Other
Intervention Name(s)
Control: Lifestyle counseling
Intervention Description
Conseling on physical activity and nutrition (intervention)
Primary Outcome Measure Information:
Title
Weight reduction
Description
Measurement by kilograms
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Increase steps/day
Description
Steps/day by accelerometer
Time Frame
1 year
Title
Decrease sedestation minute week
Description
Minutes week in sedentary activity by Activpal monitor
Time Frame
1 year
Title
Decrease total caloric intake/day
Description
Calories/day by Food frecuency questionnaire
Time Frame
1 year
Title
Improve Quality of life
Description
Measurement by IWQOL-L
Time Frame
1 year
Title
Augmentation index
Description
Central and peripheral augmentation index
Time Frame
1 year
Title
Adiponectin
Description
Inflammation marker
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Obese subjects (IMC ≥ 27.5 to <40), classified as sedentary according to the short physical activity questionnaire validated in the EVIDENT II study.
Exclusion Criteria:
Older than 65 years are excluded, due to difficulties in the use of ICTs.
Advanced respiratory, renal or liver disease.
Several mental illness
Coronary or cerebrovascular atherosclerotic disease, grade II or higher NYHA heart failure.
Moderate or severe COPD
Muscular-skeletal pathology that inhibit mobility
Subjects who can not exercise or follow a hypocaloric diet.
Oncologic disease in treatment diagnosed in the last 5 years.
Terminal situation
Pregnancy
Bariatric surgery
Those with any other circumstance that the investigators consider could interfere with the study procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luis Garcia Ortiz, MD, PhD
Organizational Affiliation
Fundacion Infosalud
Official's Role
Principal Investigator
Facility Information:
Facility Name
Primary Care Research Unit - The Alamedilla Center for Health
City
Salamanca
ZIP/Postal Code
37006
Country
Spain
12. IPD Sharing Statement
Citations:
PubMed Identifier
35103609
Citation
Lugones-Sanchez C, Recio-Rodriguez JI, Agudo-Conde C, Repiso-Gento I, G Adalia E, Ramirez-Manent JI, Sanchez-Calavera MA, Rodriguez-Sanchez E, Gomez-Marcos MA, Garcia-Ortiz L; EVIDENT 3 Investigators. Long-term Effectiveness of a Smartphone App Combined With a Smart Band on Weight Loss, Physical Activity, and Caloric Intake in a Population With Overweight and Obesity (Evident 3 Study): Randomized Controlled Trial. J Med Internet Res. 2022 Feb 1;24(2):e30416. doi: 10.2196/30416.
Results Reference
derived
PubMed Identifier
35057451
Citation
Lugones-Sanchez C, Recio-Rodriguez JI, Menendez-Suarez M, Saz-Lara A, Ramirez-Manent JI, Sanchez-Calavera MA, Gomez-Sanchez L, Rodriguez-Sanchez E, Garcia-Ortiz L, Evident Investigators Group. Effect of a Multicomponent mHealth Intervention on the Composition of Diet in a Population with Overweight and Obesity-Randomized Clinical Trial EVIDENT 3. Nutrients. 2022 Jan 9;14(2):270. doi: 10.3390/nu14020270.
Results Reference
derived
PubMed Identifier
33242020
Citation
Lugones-Sanchez C, Sanchez-Calavera MA, Repiso-Gento I, Adalia EG, Ramirez-Manent JI, Agudo-Conde C, Rodriguez-Sanchez E, Gomez-Marcos MA, Recio-Rodriguez JI, Garcia-Ortiz L; EVIDENT 3 Investigators. Effectiveness of an mHealth Intervention Combining a Smartphone App and Smart Band on Body Composition in an Overweight and Obese Population: Randomized Controlled Trial (EVIDENT 3 Study). JMIR Mhealth Uhealth. 2020 Nov 26;8(11):e21771. doi: 10.2196/21771.
Results Reference
derived
PubMed Identifier
29480874
Citation
Recio-Rodriguez JI, Gomez-Marcos MA, Agudo-Conde C, Ramirez I, Gonzalez-Viejo N, Gomez-Arranz A, Salcedo-Aguilar F, Rodriguez-Sanchez E, Alonso-Dominguez R, Sanchez-Aguadero N, Gonzalez-Sanchez J, Garcia-Ortiz L; EVIDENT 3 investigators. EVIDENT 3 Study: A randomized, controlled clinical trial to reduce inactivity and caloric intake in sedentary and overweight or obese people using a smartphone application: Study protocol. Medicine (Baltimore). 2018 Jan;97(2):e9633. doi: 10.1097/MD.0000000000009633.
Results Reference
derived
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Effectiveness to Weight Loss in Sedentary and Overweight People Using a Smartphone Application.
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