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Improvement of Physical and Physiological Parameters Through the Use of a Mobile App

30 september 2022 uppdaterad av: Prof. Dr. Alejandro Martínez-Rodríguez, University of Alicante

Study of Physical and Physiological Changes Through the Use of a Mobile App That Promotes Healthy Habits

To investigate the health effects of a new mobile application (app) for prevention and personalized treatment in people with chronic cardiovascular pathologies associated with body composition.

Studieöversikt

Detaljerad beskrivning

Scientific evidence has shown that the adoption of the Mediterranean diet is a protective factor against the appearance of several types of cancer, cardiovascular diseases, aging and obesity due to the amount of nutrients with anti-cancer, anti-inflammatory and anti-obesity properties that jointly contribute to the maintenance of health status. The antitumor effects of the Mediterranean diet are mainly due to the combination of antioxidant elements, fiber and polyunsaturated fats. Therefore, this dietary pattern is essential as a preventive measure against the onset of cancer and other chronic diseases, but also to reduce health care costs.

Monitoring physical activity should be considered as a central factor when addressing precision nutrition. Perform physical activity and exercise, as they are key components of energy expenditure and balance, in addition, structural changes occur in muscles, increase in the number of mitochondria in fiber, secretion of metabolically beneficial hormones with reversal of muscle insulin resistance and reduction of hepatic lipogenesis. Regardless of intensity, short-term exercise has been shown to improve adiposity and insulin sensitivity, which may help reduce metabolic risk. Boutcher et al. also demonstrated that intermittent aerobic and anaerobic exercise performed at an intensity >70% of maximal oxygen uptake significantly reduces ambulatory and office blood pressure in hypertensive individuals.

The development of this app aims, through self-management and visualizing the altered parameters and how they will evolve in your body in the short, medium and long term, to increase the population's commitment to these pathologies, in order to improve their health.

Studietyp

Interventionell

Inskrivning (Faktisk)

70

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Alicante
      • Elche, Alicante, Spanien, 03202
        • Nutrición Selecta

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

21 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Men and women over 21 years of age

Exclusion Criteria:

  • Volunteers who do not have access to a smartphone.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Förebyggande
  • Tilldelning: Icke-randomiserad
  • Interventionsmodell: Sekventiell tilldelning
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Aktiv komparator: CONTROL GROUP
Recommendations on healthy eating habits based on the Mediterranean diet and moderate physical activity.
Intervention based on measurements of health parameters before and after providing participants with personalized dietary and physical activity recommendations.
Experimentell: APP GROUP
Recommendations on healthy eating habits based on the Mediterranean diet and moderate physical activity through the use of an app based on machine learning, so they have constant stimuli for the improvement of the parameters.

Use of a mobile application based on machine learning with the aim of improving health parameters and body composition.

Specific diet program and moderate physical activity, all guided and mediated by a mobile application. As well as the recording and monitoring of periodic evaluations of health indicators.

Andra namn:
  • Nutritional and physical activity intervention through the use of an app.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
WEIGHT WEIGHT WEIGHT WEIGHT WEIGHT
Tidsram: 24 months
The weight of the subjects will be obtained using the TANITA (Tokyo, Japan).
24 months
HEIGHT
Tidsram: 24 months
The height of the subjects will be measured with the SECA 123 stadiometer (Hamburg, Germany).
24 months
WAIST CIRCUMFERENCE
Tidsram: 24 months
The kinanthropometric evaluation is based on the methodology proposed for the restricted profile by the International Society for the Development of Kinanthropometry (ISAK). The material used to measure the perimeters will be a tape.
24 months
HIP CIRCUMFERENCE
Tidsram: 24 months
The kinanthropometric evaluation is based on the methodology proposed for the restricted profile by the International Society for the Development of Kinanthropometry (ISAK). The material used to measure the perimeters will be a tape.
24 months
CHOLESTEROL
Tidsram: 24 months
The blood cholesterol level is obtained through a blood test.
24 months
TRIGLICERIDES
Tidsram: 24 months
The blood triglicerides level is obtained through a blood test.
24 months
BLOOD PREASURE
Tidsram: 24 months
Measurement of blood pressure (systolic and diastolic) with a digital tensiometer.
24 months
FAT MASS
Tidsram: 24 months
Assessment of body composition using the TANITA (Tokyo, Japan) validated bioimpedance scale to obtain the results of fat mass.
24 months
LEAN BODY MASS
Tidsram: 24 months
Assessment of body composition using the TANITA (Tokyo, Japan) validated bioimpedance scale to obtain the results of lean body mass.
24 months
VISCERAL FAT
Tidsram: 24 months
Assessment of body composition using the TANITA (Tokyo, Japan) validated bioimpedance scale to obtain the results of visceral fat.
24 months
HEART RATE
Tidsram: 24 months
Heart rate measurement is performed with an activity wristband.
24 months
TROPONIN I
Tidsram: 24 months
The troponin I level is obtained through a blood test.
24 months
BLOOD TROPONIN T LEVELS
Tidsram: 24 months
The troponin I level is obtained through a blood test.
24 months
Broadband ultrasonic attenuation, BUA
Tidsram: 24 months
The measurement of the ultrasonic band attenuation (BUA) by the traversed bone tissue (calcaneus) is performed using the GE Achilles Insight device.
24 months
Ultrasonic wave propagation speed, SOS
Tidsram: 24 months
The measurement of ultrasonic wave propagation speed (SOS) by the traversed bone tissue (calcaneus) is performed using the GE Achilles Insight device.
24 months

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Javier Sánchez Sánchez, Full, European University of Madrid

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 juli 2020

Primärt slutförande (Faktisk)

30 december 2021

Avslutad studie (Faktisk)

30 december 2021

Studieregistreringsdatum

Först inskickad

30 september 2021

Först inskickad som uppfyllde QC-kriterierna

13 oktober 2021

Första postat (Faktisk)

26 oktober 2021

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

3 oktober 2022

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

30 september 2022

Senast verifierad

1 september 2022

Mer information

Termer relaterade till denna studie

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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