- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05485402
Dietary Strategy to Tackle Sarcopenia in Early Elderly Subjects (FOOP-Sarc) (FOOP-Sarc)
Foods Such as Virgin Olive Oil Rich in Phenolic Compounds, and Prebiotic Supplementation: Dietary Strategy to Tackle Sarcopenia in Early Elderly Subjects (FOOP-Sarc)
The main objective of the present study is to add knowledge of the potential health effects and mechanism of action by a dietary strategy based on a VOO rich in phenolic compounds (156 mg hydroxytyrosol and tyrosol/kg oil) alone or combination with prebiotic supplementation based on fructooligosaccharides (FOS) and inulin to tackle sarcopenia by improving skeletal muscle mass and function and CVD risk factors in early elderly (60-80 years) home-dwelling sarcopenic subjects.
The specific objectives:
- To determine the compliance food intake biomarkers of VOO in 24h urine samples and prebiotic intake in faecal samples.
- To evaluate the effect of the NFOC-diet supplemented by VOO rich in phenolic compounds (156 mg hydroxytyrosol and tyrosol/kg oil) alone or in combination with prebiotic supplementation (FOS and inulin) on the improvement of muscle mass, muscle performance, gait performance, cardiovascular disease risk factors (inflammation, oxidation and endothelial function), and gut microbiota, in sarcopenic young-elderly subjects.
- To assess the mechanisms of action of the NFOC-diet supplemented by VOO rich in phenolic compounds (156 mg hydroxytyrosol and tyrosol/kg oil) alone or in combination with prebiotic supplementation (FOS and inulin) involved in the development of sarcopenia and cardiovascular disease in vivo and in vitro cellular models.
- To determine if the effects achieved after the intervention (12 weeks of intervention) will be sustained 12 weeks after the FOOP-Sarc intervention cessation (12 weeks of intervention + 12 weeks of follow-up), by assessing the sarcopenia and CVD risk factors in sarcopenic early elderly subjects.
- To co-create nutritional and physical activity recommendations of FOOP-Sarc study based on sarcopenia improvement by a sample of volunteers of the FOOP-Sarc study, and to assess the adherence and the effectivity of the recommendations, in comparison to standard recommendations created by researchers, the satisfaction and engagement experience in a co-creation process, and the usability of recommendations.
Study Overview
Status
Conditions
Intervention / Treatment
- Dietary supplement: Maltodextrin
- Other: Nutritional and physical activity recommendations
- Dietary supplement: Prebiotic (FOS and inulin)
- Dietary supplement: Refined olive oil (38.6 mg hydroxytyrosol and tyrosol/kg oil)
- Dietary supplement: Virgin olive oil rich in phenolic compounds (156 mg hydroxytyrosol and tyrosol/kg oil)
Detailed Description
The prebiotic supplementation about FOS and inulin was related to gut microbiota transformation an increase in handgrip strength and a reduction of exhaustion in older adults over 65 years old.
In the role of a nutritional intervention for the treatment of sarcopenia, an adequate intake of protein, especially leucine, vitamin D and antioxidant nutrients are recommended. In particular, dietary protein is a key anabolic stimulus for muscle protein synthesis. Moreover, food such as, virgin olive oil (VOO) can be involved in sarcopenia, by modulation of pro-inflammatory cytokines and could attenuate sarcopenic symptomology.
On the other hand, physical activity (PA) is an important aspect to avoid loss of muscle mass, for this reason, in sarcopenic subjects it is recommended to spend 150 min/week of moderate to vigorous physical activity.
A total of 135 home-dwelling early elderly volunteers will be included in the intervention (45 in each arm of the intervention). The total duration of the study will be 24 weeks (12-week period of dietary-lifestyle treatment and a 12-week period of follow-up after intervention cessation). Additionally, a total of 36 home-dwelling early elderly volunteers will be included in the co-creation process. Specifically, 12 home-dwelling early elderly volunteers will participate in the co-ideation and co-design steps. Additionally, 24 home-dwelling early elderly volunteers will participate in the co-implementation and comparison of recommendations (12 in each arm of intervention). The sample of volunteers that will co-implement will be randomized and different from the sample of volunteers that will co-ideate and co-design the recommendations. The co-evaluation step will include all 36 volunteers from the different steps of the co-creation process.
During the preliminary co-creation phase, there will be 5 visits over 5 weeks. The study visits will be the following: screening visit (V0): to check inclusion/exclusion criteria and, in case of satisfying the inclusion criteria; visits during the intervention (V1, V2, V3); and final study visit (V4). The volunteers that will co-ideate and co-design the recommendations will carry out only the V0, V1, V2, and V4. Instead, the co-implement volunteers will carry out only the visits V0, V3, and V4.
Additionally, during the FOOP-Sarc study, there will be 7 visits in total (6 visits during the intervention period and 1 follow-up visit). Of these visits, 4 will be face-to-face and 3 by telephone. The study visits will be the following: screening visit (V0, face-to-face): to check inclusion/exclusion criteria and, in case of satisfying the inclusion criteria; basal visit (V1); visits during the intervention (V2, telephone; V3, telephone; V4, telephone); final study visit (V5, face-to-face); and follow-up visit (V6, face-to-face): follow-up visit 12-week after intervention cessation. In visits V0, V1, V5, and V6 volunteers must present themselves in fasting conditions of 8 hours to obtain blood. In visits V1, V5, and V6 volunteers must bring urine and feaces samples.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rosa Solà, Dr
- Phone Number: 0034 977 75 9369
- Email: rosa.sola@urv.cat
Study Contact Backup
- Name: Rosa Maria Valls, Dr
- Phone Number: 0034 977 759 375
- Email: rosamaria.valls@urv.cat
Study Locations
-
-
Tarragona
-
Reus, Tarragona, Spain, 43201
- Recruiting
- Universitat Rovira i Virgili
-
Contact:
- Rosa Solà, Dr
- Phone Number: 0034 977 75 9369
- Email: rosa.sola@urv.cat
-
Contact:
- Rosa Maria Valls, Dr
- Phone Number: 0034 977 759 375
- Email: rosamaria.valls@urv.cat
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Men and women with and age equal to or greater than 60 years and until 80 years.
- Written informed consent provided before the initial visit.
- Sarcopenia assessment: low muscle strength based on grip dynamometry, kg (men <30 kg; women <20 kg) or low skeletal muscle mass index (SMI) based on bioimpedance analysis (BIA), kg/m2 (men <8,87 kg/m2; women <6,42 kg/m2) or low physical performance or physical function based on 4m gait speed, m/s (≤0,8 m/s)
Exclusion Criteria:
- Type 2 or insulin-dependent diabetes diagnosed.
- Anemia (hemoglobin ≤13 g/dL in men and ≤12 g/dL in women).
- Intestinal malabsorption diseases.
- Fructose and/or sucrose intolerance.
- Malnutrition (assessed by albumin <3,5 g/dl).
- Renal diseases.
- Chronic alcoholism.
- Current or past participation in a clinical trial or consumption of a research product in the 30 days prior to inclusion in the study.
- Institutionalized elderly.
- Failure to follow the study guidelines.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: Control group (Group A)
Refined olive oil (38.6 mg hydroxytyrosol and tyrosol/kg oil), maltodextrin, and nutritional and physical activity recommendations
|
The dosage will be 7,5 g/day of maltodextrin.
The nutritional recommendations are based on DASH diet and foods rich in protein (in particular, leucine) and vitamin D, polyunsaturated acids, phosphorus and iron.
The physical activity recommendations are 150 min/week of physical activity, with at least two sessions dedicated to the development of motor strength.
The dosage will be 30 ml/day of refined olive oil (38.6 mg hydroxytyrosol and tyrosol/kg oil) used as a dressing (without heat).
|
Experimental: Intervention group (Group B)
Virgin olive oil rich in phenolic compounds (156 mg hydroxytyrosol and tyrosol/kg oil), maltodextrin, and nutritional and physical activity recommendations
|
The dosage will be 7,5 g/day of maltodextrin.
The nutritional recommendations are based on DASH diet and foods rich in protein (in particular, leucine) and vitamin D, polyunsaturated acids, phosphorus and iron.
The physical activity recommendations are 150 min/week of physical activity, with at least two sessions dedicated to the development of motor strength.
The dosage will be 30 ml/day of virgin olive oil rich in phenolic compounds (156 mg hydroxytyrosol and tyrosol/kg oil) used as a dressing (without heat).
|
Experimental: Intervention group (Group C)
Virgin olive oil rich in phenolic compounds (156 mg hydroxytyrosol and tyrosol/kg oil), prebiotic supplementation (FOS and inulin), and nutritional and physical activity recommendations
|
The nutritional recommendations are based on DASH diet and foods rich in protein (in particular, leucine) and vitamin D, polyunsaturated acids, phosphorus and iron.
The physical activity recommendations are 150 min/week of physical activity, with at least two sessions dedicated to the development of motor strength.
The dosage will be 7,5 g/day of prebiotic supplement (FOS and inulin).
The dosage will be 30 ml/day of virgin olive oil rich in phenolic compounds (156 mg hydroxytyrosol and tyrosol/kg oil) used as a dressing (without heat).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in muscle mass
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
The change in muscle mass will be assessed by Magnetic Nuclear Resonance (MNR) measured lumbar 3rd vertebra.
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Body-weight
Time Frame: Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Measured with calibrated scale in kg
|
Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Height
Time Frame: Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Measured with wall-mounted stadiometer in cm
|
Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Body Mass Index
Time Frame: Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Calculated by weight (kg) divided to height (m2)
|
Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
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Body weight composition
Time Frame: Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Measured by bioimpedance (Tanita SC 330-S)
|
Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Waist circumference
Time Frame: Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Steel measuring tape at the umbilicus in cm.
|
Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Sarcopenia assessment_skeletal muscle strength
Time Frame: Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
grip strength, kg: Handheld dynamometer and the maximum value from either hand will be analyzed (Jamar dynamometer; Sammons Preston Rolyan, Bolingbrook, IL)
|
Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Sarcopenia assessment_muscle mass
Time Frame: Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Muscle mass, wasting and turnover: assessed by Magnetic Nuclear Resonance (MNR) measured lumbar 3rd vertebra
|
Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Sarcopenia assessment_muscle physical performance
Time Frame: Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Gait speed, m/s: length of the walking course divided by the time
|
Visit 0 (week -1), visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Compliance of physical activity recommendations
Time Frame: Visit 1 (week 0), visit 2 (week 2), visit 3 (week 4), visit 4 (week 6) visit 5 (week 8), visit 6 (week 10), visit 7 (week 12), visit 8 (week 24)
|
IPAQ-E Spanish version
|
Visit 1 (week 0), visit 2 (week 2), visit 3 (week 4), visit 4 (week 6) visit 5 (week 8), visit 6 (week 10), visit 7 (week 12), visit 8 (week 24)
|
Compliance of the dietary recommendations
Time Frame: Visit 1 (week 0), visit 2 (week 2), visit 3 (week 4), visit 4 (week 6) visit 5 (week 8), visit 6 (week 10), visit 7 (week 12), visit 8 (week 24)
|
Dietary record: 3-day dietary record
|
Visit 1 (week 0), visit 2 (week 2), visit 3 (week 4), visit 4 (week 6) visit 5 (week 8), visit 6 (week 10), visit 7 (week 12), visit 8 (week 24)
|
Dietary compliance markers
Time Frame: Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Folin-Ciocalteau method adjusted by creatinine values, measured in 24h urine samples
|
Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Specific phenolic compounds_dietary compliance markers
Time Frame: Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Specific phenolic compounds and metabolites assessed by Ultra performance liquid chromatography - tandem mass spectrometer (UPLC-MS/MS) in urine samples
|
Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Phenolic metabolites_dietary compliance markers
Time Frame: Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Phenolic metabolites by UPLC-MS/MS in plasma
|
Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Sarcopenia and Quality of life
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
SarQoL® test assessed by quality of life test adapted to sarcopenic subjects.
It is scored from 0 to 100, where higher values indicate better quality of life.
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Fasting blood glucose (FBG)
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
by standardized methods in an automated analyzer (Beckman Coulter-Synchron, Galway, Ireland) in (mmol/L)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Insulin
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
by standardized methods in an automated analyzer (Beckman Coulter-Synchron, Galway, Ireland) in (IU/mL)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Homeostasis model assessment index (HOMA index)
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Calculated by fasting insulin (μUI/mL) x fasting glucose (mmol/L) / 22,5
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Lipid profile
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Total cholesterol (TC), high density lipoprotein cholesterol (HDLc), low density lipoprotein cholesterol (LDLc) and Total triglycerides (TG) in mmol/L by standardized enzymatic automated methods in an autoanalyzer (Beckman Coulter-Synchron, Galway, Ireland)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Apolipoproteins
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Apolipoprotein A1 (ApoA1) and apolipoprotein B100 (ApoB100) in mg/dL by standardized enzymatic automated methods in an autoanalyzer (Beckman Coulter-Synchron, Galway, Ireland)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Apolipoproteins ratio
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Calculated by ApoA1 divided to ApoB100
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Vascular parameters_endothelial function
Time Frame: Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Ischemic reactive hyperemia (IRH) with Laser-Doppler Linear Periflux 5000 (Perimed AB, Järfälla, Stockholm, Sweden)
|
Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Vascular parameters_blood pressure
Time Frame: Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Systolic blood pressure (SBP) and Diastolic blood pressure (DBP) in mm Hg by automatic sphygmomanometer (OMRON HEM-907; Peroxfarma, Barcelona, Spain).
|
Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Vascular parameters_pulse pressure
Time Frame: Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Calculated by SBP - DBP
|
Visit 1 (week 0), visit 3 (week 4), visit 5 (week 8), visit 7 (week 12), visit 8 (week 24)
|
Endothelin
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Endothelin in pg/mL assessed by Commercial ELISA
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Endothelial dysfunction markers
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
E-selectin (CD62E), P-selectin (CD62P), Intercellular Cell Adhesion Molecule 1 (ICAM-1 (CD54)) and Vascular Cell Adhesion Molecule 1 (VCAM-1 (CD106) assessed by multi-analyte ELISArray kits.
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Oxidative biomarkers_Oxidized LDL
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Oxidized LDL (oxLDL) assessed by commercial ELISA.
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Oxidative biomarkers_Superoxide Dismutase
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Superoxide Dismutase (SOD) in U/g Hb assessed by enzymatic assay
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Oxidative biomarkers_Glutathione peroxidase
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Glutathione peroxidase (GSHPx) in nmol/mL assessed by enzymatic assay
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Inflammation biomarkers_High sensitivity C-reactive protein
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
High sensitivity C-reactive protein (hsCRP) in mg/L assessed by Immunoturbidimetry on an autoanalyzer (Roche Diagnostics Systems, Madrid, Spain)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Inflammation biomarkers_interleukine-6
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Interleukine-6 (IL-6) in pg/mL assessed by Immunoturbidimetry on an autoanalyzer (Roche Diagnostics Systems, Madrid, Spain)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Inflammation biomarkers_uric acid
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Uric acid in mg/dL is assessed by Immunoturbidimetry on an autoanalyzer (Roche Diagnostics Systems, Madrid, Spain)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Inflammation biomarkers_tumour necrosis factor-α
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Tumour necrosis factor-α (TNF-α) in pg/mL is assessed by commercial ELISA kit.
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Renal function_creatinine
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Creatinine in mg/dL is assessed by standardized methods in a Cobas Mira Plus autoanalyzer (Roche Diagnostics Systems, Madrid, Spain) in 24 h urine samples
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Renal function_glomerular filtration rate
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Glomerular filtration rate (GFR) in mL/minutes/1.73m2 is assessed by equation Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI).
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Endocrine system
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Testosterone (pg/mL) and growth hormone (GH) (pg/mL)) assessed by in a Cobas Mira Plus autoanalyzer (Roche Diagnostics Systems, Madrid, Spain)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Proteome profiling
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Whole proteome assessed by nano Liquid chromatography-mass spectrometry (nLC-MS) according to our previous work.
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Gut microbiota_phyla composition and functionality
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Phyla composition and functionality assessed by whole genomic content sequencing.
Illumina platform will be used to obtain the metagenomics and metatranscriptomics of each sample following previous protocols developed in Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO-Salud Pública (Valencia)).
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Gut microbiota_short chain fatty acids
Time Frame: Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Short chain fatty acids (SCFA): bile acids, sterols, buthyrate, and branched chain amino acids and sterols assessed by gas chromatography (GC)
|
Visit 1 (week 0), visit 7 (week 12), visit 8 (week 24)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rosa Solà, Dr, University Rovira i Virgili, Reus, Tarragona, Spain
- Principal Investigator: Rosa Maria Valls, Dr, University Rovira i Virgili, Reus, Tarragona, Spain
Publications and helpful links
General Publications
- Cruz-Jentoft AJ, Bahat G, Bauer J, Boirie Y, Bruyere O, Cederholm T, Cooper C, Landi F, Rolland Y, Sayer AA, Schneider SM, Sieber CC, Topinkova E, Vandewoude M, Visser M, Zamboni M; Writing Group for the European Working Group on Sarcopenia in Older People 2 (EWGSOP2), and the Extended Group for EWGSOP2. Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing. 2019 Jan 1;48(1):16-31. doi: 10.1093/ageing/afy169. Erratum In: Age Ageing. 2019 Jul 1;48(4):601.
- Beaudart C, Biver E, Reginster JY, Rizzoli R, Rolland Y, Bautmans I, Petermans J, Gillain S, Buckinx F, Dardenne N, Bruyere O. Validation of the SarQoL(R), a specific health-related quality of life questionnaire for Sarcopenia. J Cachexia Sarcopenia Muscle. 2017 Apr;8(2):238-244. doi: 10.1002/jcsm.12149. Epub 2016 Oct 22.
- Rubio Castaneda FJ, Tomas Aznar C, Muro Baquero C. [Validity, Reliability and Associated Factors of the International Physical Activity Questionnaire Adapted to Elderly (IPAQ-E)]. Rev Esp Salud Publica. 2017 Jan 18;91:e201701004. Spanish.
- Ignacio de Ulibarri J, Gonzalez-Madrono A, de Villar NG, Gonzalez P, Gonzalez B, Mancha A, Rodriguez F, Fernandez G. CONUT: a tool for controlling nutritional status. First validation in a hospital population. Nutr Hosp. 2005 Jan-Feb;20(1):38-45.
Study record dates
Study Major Dates
Study Start (Actual)
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
Keywords
Additional Relevant MeSH Terms
- Nervous System Diseases
- Neurologic Manifestations
- Neuromuscular Manifestations
- Pathological Conditions, Anatomical
- Muscular Atrophy
- Atrophy
- Sarcopenia
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Anti-Arrhythmia Agents
- Anti-Infective Agents, Local
- Anti-Infective Agents
- Platelet Aggregation Inhibitors
- Protective Agents
- Antioxidants
- Disinfectants
- 3,4-dihydroxyphenylethanol
- Phenylethyl Alcohol
- 4-hydroxyphenylethanol
Other Study ID Numbers
- FOOP-Sarc study
- PID2019-105164RB-I00 (Other Grant/Funding Number: MCIN/AEI/10.13039/501100011033)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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