Results at 10 Years of the RESOLVE Study (RESOLVE+10) (RESOLVE+10)

June 29, 2020 updated by: University Hospital, Clermont-Ferrand

Results at 10 Years of the RESOLVE Study (REverse Metabolic SyndrOme by Lifestyle and Various Exercise)

10-year effect of a lifestyle intervention program (exercise, sedentary lifestyle and dietary diet) on abdominal visceral adipose tissue (primary endpoint of the RESOLVE study 10 years ago): influence of kinetics abdominal visceral adipose tissue loss in the first year of follow-up on abdominal visceral adipose tissue at 10 years

Study Overview

Detailed Description

The RESOLVE + 10 protocol was design to provide a 10-year effect of a lifestyle intervention program (exercise, sedentary lifestyle and dietary diet) on abdominal visceral adipose tissue.

In the present protocol, parameters are measured just once, during 3 hours, to compared the results with those of the protocol RESOLVE (5 measurement times over a year 10 years ago: before the thermal modification program of the lifestyle ( exercise, sedentary lifestyle and diet) of 3 weeks (D0), after the thermal program (D21), at the 3rd month (M3), 6th month (M6) and 12th month of follow-up (M12), to which was matched a healthy control group).

Statistical analysis will be performed using Stata software (version 13; Stata-Corp, College Station, Tex., USA). All statistical tests will be two-sided and p inferior to 0.05 will be considered significant. Qualitative variables will be described in terms of numbers and proportions. Quantitative variables will be described in terms of numbers, mean standard deviation or median according to statistical distribution (normality studied using Shapiro-Wilk test). Graphic representations will be complete presentations of results. Comparisons between patients and controls, concerning loss of abdominal visceral adipose tissue at 10 years, will be performed using Student t-test or Mann-Whitney test if the assumptions of anova are not met (normality and homoscedasticity analyzed using Fisher-Snedecor test). The results will be expressed as effect-size and 95 percent confidence intervals. The primary analysis should be completed by multivariable analysis (linear regression with logarithmic transformation of dependent outcome if necessary) considering an adjustment on covariates fixed according to univariate results and clinical relevance. The results will be expressed as regression coefficients and 95percent confidence intervals. Furthermore, the abdominal visceral adipose tissue loss kinetics in the first year of follow-up will be considered an independent variable and treated as a functional variable. The intra-group comparisons (for patients and for controls) will be performed using paired statistical tests: paired t-test or Wilcoxon test. The results will be expressed as effect-size and 95 percent confidence intervals. Comparisons between independent groups will be done similarly as presented previously for other quantitative outcomes (body composition, quality of life, skin conductance, etc.). Multivariable analyses will be applied similarly as described previously. The comparisons concerning categorical variables will be realized using Chi-squared or when appropriate Fischer-exact test. The relations between quantitative outcomes will be analyzed using correlation coefficients (Pearson or Spearman according to statistical distribution). Considering the several multiple comparisons, a correction of the type I error will be applied (Sidak's correction).

Study Type

Interventional

Enrollment (Anticipated)

150

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Clermont-Ferrand, France, 63000
        • CHU de Clermont-Ferrand

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years to 70 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • patients and healthy controls included in the RESOLVE study

Exclusion Criteria:

  • refusal of participation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
NO_INTERVENTION: control group
no intervention
EXPERIMENTAL: Re group
high-Resistance-moderate-endurance, participants performed 10 repetitions at 70% of one maximal repetition in resistance and 30% of VO2-peak for endurance training

3-week residential program based on a tryptic (diet, exercise, education). The three weeks intervention was followed by a 1-year at-home follow-up.

In the original protocol, participants were involved in a 3-week residential program based on a tryptic (diet, exercise, education).

EXPERIMENTAL: rE group
moderate-resistance (30%) - high-Endurance (70%)

3-week residential program based on a tryptic (diet, exercise, education). The three weeks intervention was followed by a 1-year at-home follow-up.

In the original protocol, participants were involved in a 3-week residential program based on a tryptic (diet, exercise, education).

EXPERIMENTAL: re group
moderate-resistance (30%) - moderate-endurance (30%).

3-week residential program based on a tryptic (diet, exercise, education). The three weeks intervention was followed by a 1-year at-home follow-up.

In the original protocol, participants were involved in a 3-week residential program based on a tryptic (diet, exercise, education).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Abdominal visceral adipose tissue loss, a primary cardiovascular risk (CVR) factor, highly related to morbidity and mortality
Time Frame: Year 10
to assess the ability of a lifestyle program in decreasing abdominal visceral fat, one of the major health-related factor It will be assessed from dual-energy X-ray absorptiometry
Year 10

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
weight
Time Frame: Year 10
measured in kilogramms
Year 10
systolic blood pressure
Time Frame: Year 10
measured in millimeter of mercure
Year 10
diastolic blood pressure
Time Frame: Year 10
measured in millimeter of mercure
Year 10
Waist circumference
Time Frame: Year 10
measured in centimeter
Year 10
heart rate
Time Frame: Year 10
measured in battment per minutes
Year 10
Muscle mass
Time Frame: Year 10
measured using Impedancemeter, Densitometry x-ray absorption, Peripheral quantitative computed tomography (pQCT) and Quantitative ultrasounds (QUS)
Year 10
fat mass
Time Frame: Year 10
measured using Impedancemeter, Densitometry x-ray absorption, Peripheral quantitative computed tomography (pQCT) and Quantitative ultrasounds (QUS)
Year 10
bone structure
Time Frame: Year 10
measured using Impedancemeter, Densitometry x-ray absorption, Peripheral quantitative computed tomography (pQCT) and Quantitative ultrasounds (QUS)
Year 10
Epicardial adipose tissue
Time Frame: Year 10
measures of epicardial adipose tissue using Magnetic resonance imaging (MRI) and echocardiography
Year 10
myocardial triglycerides
Time Frame: Year 10
measures of myocardial triglycerides using MRI
Year 10
cardiac remodeling and function
Time Frame: Year 10
measures cardiac remodeling and function using MRI and echocardiography)
Year 10
Depression
Time Frame: Year 10
Assessing depression using Hospital anxiety and depression scale- HAD. It's a 14-item questionnaire about frequency of perception about anxious (HAD-A: 7 items) and depressive (HAD-D: 7 items) symptoms. Items are made of a 4-point scale frequency of symptoms, varying from "never" to "always". Scores higher than 8 for HAD-A or HAD-D mean a possible symptomatology, and scores higher than 11 mean a clear and proper diagnostic of depressive or anxious disorder.
Year 10
anxiety
Time Frame: Year 10
Assessing anxiety using State and trait anxiety inventory which consists of separate self-report scales measuring to distinct anxiety concepts: state anxiety and trait anxiety. Both state and trait anxiety are explored by a 20-item questionnaire made of a 4-point scale from "never" to "always".
Year 10
General health
Time Frame: Year 10
Assessing general health using General Health Questionnaire with 36 items (SF-36)
Year 10
Stress
Time Frame: Year 10
Assessing stress using visual analog scale of 100 mm, ranging from very low (0) to very high (100).
Year 10
Fatigue
Time Frame: Year 10
Assessing fatigue using visual analog scale of 100 mm, ranging from very low (0) to very high (100).
Year 10
Sleep
Time Frame: Year 10
Assessing sleep using visual analog scale of 100 mm, ranging from very low (0) to very high (100).
Year 10
Burnout
Time Frame: Year 10
Assessing burnout using Maslach Burnout Inventory, composed of 22 items designed to assess the three components of the burn-out syndrome: emotional exhaustion (9 items), depersonalization (5 items) and reduced personal accomplishment (8 items). Items are made of a 7-point scale frequency of feelings, varying from "never" to "every day". The scores for each component of the burn-out syndrome are considered separately and are not combined into a single total score. If desired for participant feedback, each score can be coded as low, average, or high.
Year 10
Mindfulness
Time Frame: Year 10
Assessing mindfulness using Freiburg Mindfulness Inventory a consistent and reliable scale evaluating several important aspects of mindfulness. Mindfulness has been described as a non-elaborative, non-judgmental present-centred awareness in which each thought, feeling or sensation that arises in the attention field is acknowledged and accepted as it is. Mindfulness appears as an attribute of consciousness long believed to promote well-being. Each self-descriptive statement of the FMI is evaluated using a four-point Likert scale ranging from 1 (strongly disagree) to 4 (strongly agree)
Year 10
Coping strategy
Time Frame: Year 10
Assessing coping using Brief COPE Questionnaire made to evaluate self-perceived reaction to a particular situation. The 28 items of the BCQ explore the 14 different theoretically identified coping responses (with two items for each of the measured coping strategies): self-distraction, active coping, denial, substance use, use of emotional support, use of instrumental support, Behavioral disengagement, venting, positive reframing, planning, humor, acceptance, religion, and self-blame. Items of BCQ are scored on a four-point Likert-type scale, ranging from 1 = strongly disagree to 4 = strongly agree.
Year 10
Emotions
Time Frame: Year 10
Assessing emotions using Emotion Regulation Questionnaire a 10-item scale designed to measure respondents' tendency to regulate their emotions in two ways: 1) cognitive reappraisal and 2) expressive suppression. Respondents answer each item on a 7-point
Year 10
Perception of work
Time Frame: Year 10
Assessing perception of work using Job Content Questionnaire of Karasek which assessed job demands, job control and social support through 26 items. The questionnaire measures 9 items of job demands, 9 items of job control and 8 items of social support. Items are scored on a four-point Likert-type scale, ranging from 1 = strongly disagree to 4 = strongly agree. Among the 26 items, 5 negative statements require reverse scoring. From French data, the job strain threshold is set for a demands score higher than 20 and a control score lower than 71; the isostrain threshold is determined from a combining score of job strain and social support lower than 24. We would ask the participants to fulfil the questionnaire from memories that they keep of their work.
Year 10
Self-efficacy
Time Frame: Year 10
Assessing self-efficacy using Perceived self-efficacy scale created to assess a general sense of perceived self-efficacy with the aim in mind to predict coping with daily hassles as well as adaptation after experiencing all kinds of stressful life events. Responses are made on a 4-point scale for the 10 items (from "false" to "true"). The final composite score (ranged from 10 to 40) is obtained by summing up the responses to all 10 items. An example of item is "I am confident that I could deal efficiently with unexpected events".
Year 10
Addiction
Time Frame: Year 10
Assessing addiction to work using Work Addiction Risk test (WART). The WART is a self-administered test with 25 statements for which the answers are scored 1-never true to 4-always true [20,26]. Respondents read the statements and mark their answers to describe their work habits [19,27]. The total score is the sum of the responses to the items-25 to 100-and the higher the score, the more one is considered addicted to work [18,21]. Scores from 25 to 56 were defined as "at low-risk of work addiction"; 57 to 66 as "at medium-risk of work addiction", and from 67 to 100 as "at high-risk of work addiction".
Year 10
Alexithymia
Time Frame: Year 10
Assessing alexithymia using Toronto Alexithymia Scale For this scale, a three-factor structure was proposed: difficulty identifying feelings, difficulty describing feelings and externally oriented thinking. Responses are made on a 5-point scale from "strongly agree" to "strongly disagree".
Year 10
Illness perception
Time Frame: Year 10
Assessing illness perception using Brief Illness Perception Questionnaire (B-IPQ), adapted for stress at work). It's a self-questionnaire comprising an 11-point scale, including 8 items measuring cognitive and emotional illness perceptions (consequences, timeline, personal control, treatment control, symptoms, coherence, illness concern and negative emotions). The total score is calculated by averaging all items (after reversed some items). A high score meant that diabetes was perceived as a threat.
Year 10
Metacognition
Time Frame: Year 10
Assessing metacognition using MetaCognition Questionnaire. It is a 30-item questionnaire made of 5-point scales. The MCQ-30 is structured in five factors: cognitive confidence, positive beliefs about worry, cognitive self-consciousness, negative beliefs about uncontrollability of thoughts and danger, and beliefs about need to control thoughts.
Year 10
Time perception
Time Frame: Year 10
Assessing time perception using Zimbardo Time Perspective Inventory, a self-reported questionnaire comprising 56 items. Responses are made on a 5-point scale from "very uncharacteristic" to "very characteristic". It explores 3 temporalities and 5 dimensions.
Year 10
Life style
Time Frame: Year 10
Assessing factors regarding lifestyle are related to smoking, alcohol, coffee, food intake (questionnaires), and physical activity (Recent Physical Activity Questionnaire)
Year 10
Treatment perception
Time Frame: Year 10
Assessing factors regarding psychology and treatment are related to perception of treatment (Beliefs about Medicines Questionnaire), adherence to treatment (Visual analog scales from never to always), barriers to treatment (QUILAM) and treatment satisfaction (treatment SATisfaction with MEDicines Questionnaire).
Year 10
questionnaires used 10 years ago
Time Frame: Year 10
Understanding and knowledge about the metabolic syndrome (4 items), comparative optimism (4 items), motivation to eat healthy (16 items) and motivation to practise physical activity (16 items).
Year 10
Cholesterol
Time Frame: Year 10
Blood analyses on HDLc and LDL-cholesterol
Year 10
HbA1c
Time Frame: Year 10
Blood analyses on HbA1c
Year 10
Triglycerides (TG)
Time Frame: Year 10
Blood analyses on Triglycerides (TG)
Year 10
Cortisol
Time Frame: Year 10
Blood analyses on Cortisol
Year 10
DHEAS
Time Frame: Year 10
Blood analyses on DHEAS
Year 10
Leptin
Time Frame: Year 10
Blood analyses on Leptin
Year 10
BDnF
Time Frame: Year 10
Blood analyses on BDnF
Year 10
Cytokines
Time Frame: Year 10
Blood analyses on Pro-inflammatory Cytokines: IL-1β, IL-6, IL-1, TNFα, NPY
Year 10
Telomeres length
Time Frame: Year 10
Blood analyses on Telomeres length
Year 10
Genetic polymorphisms related to stress
Time Frame: Year 10
Polymorphism of the angiotensin converting enzyme and Polymorphism of the serotonin are measured by Blood cells
Year 10
carotid intima-media thickness
Time Frame: Year 10
Assessing on carotid intima-media thickness by high-resolution B-mode ultrasound.
Year 10
blood flow velocity
Time Frame: Year 10
Assessing on blood flow velocity by laser speckle contrast imaging (LSCI) and microvascular perfusion by laser-doppler flowmetry (LDF), flowmotion and Iontophoresis procedure.
Year 10
microvascular perfusion
Time Frame: Year 10
Assessing microvascular perfusion by laser-doppler flowmetry (LDF).
Year 10
flowmotion
Time Frame: Year 10
Assessing flowmotion
Year 10
iontophoresis
Time Frame: Year 10
Assessing iontophoresis procedure
Year 10
heart rate variability
Time Frame: Year 10
Assessing heart rate variability by Holter
Year 10
skin conductance
Time Frame: Year 10
Assessing skin conductance by Wristband electrodes - Empatica 4.
Year 10
Quantification of liver steatosis and fibrosis
Time Frame: Year 10
Liver steatosis by MRI, fibroscanner (ultrasonic attenuation) and Aixplorer (Lipersonic Imagine®).
Year 10
Quantification of liver fibrosis
Time Frame: Year 10
Liver fibrosis by fibroscanner (liver stiffness) and fibrotest
Year 10
Vo2max
Time Frame: Year 10
Assessing factors regarding fitness are related to Vo2max (maximal exercise test)
Year 10
Fitness
Time Frame: Year 10
Assessing factors regarding fitness are related to 6-minutes walking test.
Year 10
strength
Time Frame: Year 10
Assessing factors regarding fitness are related to strength
Year 10
leptin variation
Time Frame: Year 10
Blood analyses on leptin
Year 10
ghrelin variation
Time Frame: Year 10
Blood analyses on ghrelin
Year 10
NPY variation
Time Frame: Year 10
Blood analyses on NPY
Year 10
adiponectin variation
Time Frame: Year 10
Blood analyses on adiponectin
Year 10
Evaluation of CCK level
Time Frame: Year 10
Blood analyses on CCK
Year 10
Evaluation of VEGF level
Time Frame: Year 10
Blood analyses on VEGF
Year 10
Evaluation of PAI1 level
Time Frame: Year 10
Blood analyses on PAI1
Year 10
insulin level
Time Frame: Year 10
Blood analyses on insulin
Year 10
HbA1c level
Time Frame: Year 10
Blood analyses on HbA1c
Year 10
blood glucose level
Time Frame: Year 10
Blood analyses on blood glucose
Year 10
albumin level
Time Frame: Year 10
Blood analyses on blood albumin
Year 10
transthyretin level
Time Frame: Year 10
Blood analyses on transthyretin
Year 10
Homeostasis
Time Frame: Year 10
Blood analyses on Homeostasis (Fibroblast growth factor 23)
Year 10
Osteoresorption
Time Frame: Year 10
Blood analyses on Osteoresorption (C-terminal Telopeptide of Type I collagen)
Year 10
Osteoformation
Time Frame: Year 10
Blood analyses on Osteoformation (decarboxylated osteocalcine and BSAP)
Year 10

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ANTICIPATED)

September 1, 2020

Primary Completion (ANTICIPATED)

July 1, 2021

Study Completion (ANTICIPATED)

July 1, 2021

Study Registration Dates

First Submitted

June 22, 2020

First Submitted That Met QC Criteria

June 29, 2020

First Posted (ACTUAL)

July 1, 2020

Study Record Updates

Last Update Posted (ACTUAL)

July 1, 2020

Last Update Submitted That Met QC Criteria

June 29, 2020

Last Verified

June 1, 2020

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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