- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04453098
Results at 10 Years of the RESOLVE Study (RESOLVE+10) (RESOLVE+10)
Results at 10 Years of the RESOLVE Study (REverse Metabolic SyndrOme by Lifestyle and Various Exercise)
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Clermont-Ferrand, France, 63000
- CHU de Clermont-Ferrand
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- patients and healthy controls included in the RESOLVE study
Exclusion Criteria:
- refusal of participation
Study Plan
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
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AOI 2018 DUTHEIL
- 2019-A01016-51 (OTHER: ANSM)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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