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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04315376
Other study ID # CI-08518
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 10, 2018
Est. completion date February 15, 2019

Study information

Verified date March 2020
Source University of Guadalajara
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background: Obesity is one of the most important health problems worldwide, several factors related to lifestyle as physical inactivity and unbalanced diets increase their development. This condition is characterized by low-chronic inflammation by excess of adipose tissue. The apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC) protein is part of NLRP3 inflammasome, a complex related to inflammation and metabolic alterations.

Purpose: The aim of this study was to evaluate the effect of physical exercise program on ASC gene expression and inflammatory markers in obese adults.

Methods: 37 obese individuals were randomized to exercise-diet group or diet-group during a 4-month follow-up period. The dietary evaluation was analyzed by Nutritionist Pro software. Body composition was evaluated by bioimpedance (InBody 370). All biochemical determinations were analyzed by dry chemistry (Vitros 350). ASC messenger ribonucleic acid (mRNA) expression was performed by real-time polymerase chain reaction (PCR) using Taqman probes and by the 2-ΔΔcq quantification method. Cytokine levels was performed using the Bio-PlexPro™ HumanTh17Cytokine Assays (MagPix) panel. Statistical analysis was performed with Statistical Package for the Social Sciences (SPSS) v.22 software.


Description:

A randomized clinical trial was conducted in the Institute of Translational Nutrigenetics and Nutrigenomics, Department of Molecular Biology in Medicine, Health Sciences Center, at the University of Guadalajara, Guadalajara, Jalisco, Mexico, from February of 2018 to February of 2019. All participants were recruited through flyers and social media invitations. Sample size was determined according to the mean difference formula for clinical trials. To achieve a statistical power of 80% and an alpha of 5%, a sample size of 13 participants in each study group was required. However, 37 obese individuals who met the selection criteria were randomized in exercise-diet group or diet-group. Blood sample, height and weight were measured after 8-12 hour fast and wearing light clothes. The participants in the exercise-diet group were cited in the Respiratory Unit of the University of Guadalajara with the indication of not consuming caffeine, tobacco or energy drinks 24 hours before the test, and not having eaten food at least two hours before the Astrand-rhyming Test. This study was approved by the Ethics and Biosafety Committee of the Health Sciences Center, University of Guadalajara (registry number CUCS/CINV/0476/18). The procedures were in accordance with this institution's guidelines and all the participants signed a written consent-informed.


Recruitment information / eligibility

Status Completed
Enrollment 37
Est. completion date February 15, 2019
Est. primary completion date February 15, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 50 Years
Eligibility Inclusion Criteria:

- BMI greater than 30 kg/m^2

- Sedentary individuals

- Both genres

- Waist circumference greater than 80 centimeters in women and greater than 90 centimeters in men

Exclusion Criteria:

- Pregnant or breastfeeding women

- Diagnosis of any metabolic disease or cancer

- Alcohol or tobacco consumption

- Muscle or joint injury

Study Design


Intervention

Behavioral:
Exercise-Diet Intervention
The participants who performed exercise-diet intervention performed an Astrand-rhyming test before and after the exercise program intervention. Participants followed a progressive exercise-program during four months according to initial physical fitness. The main exercises consisted of improving aerobic, speed and resistance performance. During all single sessions, breathlessness and fatigue were measured using 0 to10 Borg scale. A personal trainer certified by American College of Sports Medicine (ACSM) supervised three sessions per week, the other two unsupervised training days the subjects were given the detailed training program to do in house/park. And also, this group received a diet intervention that consisted of a 20 percentage reduction of total energy expenditure estimated by the Mifflin formula with a nutrients distribution as follows: 50% carbohydrates, 30% lipids, and 20% proteins.
Diet Intervention
This group received a diet intervention that consisted of a 20 percentage reduction of total energy expenditure estimated by the Mifflin formula with a nutrients distribution as follows: 50% carbohydrates, 30% lipids, and 20% proteins.

Locations

Country Name City State
Mexico Erika Martínez-López Guadalajara Jalisco

Sponsors (1)

Lead Sponsor Collaborator
University of Guadalajara

Country where clinical trial is conducted

Mexico, 

References & Publications (6)

ASTRAND PO, RYHMING I. A nomogram for calculation of aerobic capacity (physical fitness) from pulse rate during sub-maximal work. J Appl Physiol. 1954 Sep;7(2):218-21. — View Citation

Lin CH, Chiang SL, Tzeng WC, Chiang LC. Systematic review of impact of lifestyle-modification programs on metabolic risks and patient-reported outcomes in adults with metabolic syndrome. Worldviews Evid Based Nurs. 2014 Dec;11(6):361-8. doi: 10.1111/wvn.1 — View Citation

Ozaki E, Campbell M, Doyle SL. Targeting the NLRP3 inflammasome in chronic inflammatory diseases: current perspectives. J Inflamm Res. 2015 Jan 16;8:15-27. doi: 10.2147/JIR.S51250. eCollection 2015. Review. — View Citation

Ross R, Hudson R, Stotz PJ, Lam M. Effects of exercise amount and intensity on abdominal obesity and glucose tolerance in obese adults: a randomized trial. Ann Intern Med. 2015 Mar 3;162(5):325-34. doi: 10.7326/M14-1189. — View Citation

Taniguchi S, Sagara J. Regulatory molecules involved in inflammasome formation with special reference to a key mediator protein, ASC. Semin Immunopathol. 2007 Sep;29(3):231-8. Epub 2007 Sep 6. Review. — View Citation

You T, Arsenis NC, Disanzo BL, Lamonte MJ. Effects of exercise training on chronic inflammation in obesity : current evidence and potential mechanisms. Sports Med. 2013 Apr;43(4):243-56. doi: 10.1007/s40279-013-0023-3. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in ASC mRNA Expression The polymorphonuclear cells were separated using Dextran treatment from peripheral blood samples. Subsequently, TRIzol® reagent was using according to the manufacturer´s instructions. The complementary DNA (cDNA) synthesis was performed according to standard techniques.
Quantitative real-time PCR was performed using TaqMan® probes in Light Cycler 96 equipment considering standards PCR conditions to analyze ASC mRNA relative expression by 2-??cq method. The amplification reactions were performed in duplicate using ß-Actin gene as constitutive gene to normalized the samples.
Mean change from baseline (0 Month) to end of treatment at 4th Month.
Primary Change in Pro-inflammatory and Anti-inflammatory Cytokines The pro-inflammatory and anti-inflammatory cytokines quantification were using Bio-Plex Pro™ Human cytokine Standard 17-Plex, Group I kit following the supplier's instructions, and the read was immediately by MAGPIX™ analyzer. Mean change from baseline (0 Month) to end of treatment at 4th Month.
Primary Change in Astrand-rhyming Submaximal Test The Astrand-rhyming submaximal test was performed as described by Astrand. Mean change from baseline (0 Month) to end of treatment at 4th Month.
Secondary Changes in Height Height in meters using a stadiometer. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month. 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in Weight The weight was measured in kilograms on InBody 370. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in Body Mass Index (BMI) Weight and height were be combined to report BMI in kg/m^2 At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in Waist Circumference Waist circumference was measured at the narrowest point between the edge of the inner rib and the iliac crest, with the participant in an abducted and relaxed position, after expiration using a Lufkin Executive® tape. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in Fat Mass The Fat Mass was measured in kilograms by electrical bioimpedance on InBody 370. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in Musculoskeletal Mass The musculoskeletal mass was measured in kilograms by electrical bioimpedance on InBody 370. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in Serum Glucose It was measured in mg/dL using a dry chemistry system in Vitros 350 equipment. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in Serum Insulin Were determined through Insulin Model ELISA kit following the supplier's instructions. At the baseline (0 Month), 3th month and the 4th month.
Secondary Changes in homeostatic model assessment - insulin resistance (HOMA-IR) Serum glucose and Insulin levels were be combined to report HOMA-IR calculated as described by Matthews. At the baseline (0 Month), 3th month and the 4th month.
Secondary Changes in Total Cholesterol It was measured in mg/dL using a dry chemistry system in Vitros 350 equipment. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in High-density lipoprotein (c-HDL) It was measured in mg/dL using a dry chemistry system in Vitros 350 equipment. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
Secondary Changes in Atherogenic Index Serum total cholesterol and c-HDL were be combined to report atherogenic index, calculated through formula [Total cholesterol (mg/dL) / HDL-c (mg/dL)]. At the baseline (0 Month) and 1st month, 2nd month, 3th month and the 4th month.
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