Potential Benefits of Dietary Advices Alone or Associated to Nutraceutical Food Supplements Argan Oil, VSL#3 Probiotic Blend, 5203-L Fruit Extract Terpene
RISTOMED
Open Label, Randomized Study of the Impact of Diet on Gut Microbiota, Inflammageing and Oxidative Stress in Elderly People. Potential Benefits of Dietary Advices Alone or Associated to Nutraceutical Food Supplements Argan Oil, VSL#3 Probiotic Blend, 5203-L Fruit Extract Terpene. French Part of a Multicentric European Study
1 other identifier
interventional
48
1 country
1
Brief Summary
Ageing of the population is a major event in the world. Gerontological/geriatric literature unanimously indicate that physical exercise and diet are at present the two available fundamental approaches to contrast/prevent most of the age associated alterations. In the elderly the inflammageing, the oxidative stress and the alteration of the intestinal microbiota can be influenced by nutritional status and possibly corrected by an appropriate dietetic intervention: Nowadays the nutraceutical food supplements become an opportunity for the consumer to improve the quality of individual diet for specific needs This study will focus on the development of a specific dietary approach through an E-Health dietary service, associated or not to nutraceutical food supplements intake, to modulate the oxidative stress, inflammageing and gut microflora in the elderly people.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2010
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 15, 2010
CompletedFirst Posted
Study publicly available on registry
February 17, 2010
CompletedStudy Start
First participant enrolled
March 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2011
CompletedJune 1, 2011
May 1, 2011
1.1 years
February 15, 2010
May 31, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The primary beneficial effect parameter is hsPCR (high-sensitivity C-reactive protein)
2 months
Secondary Outcomes (6)
Inflammageing status: WBC, hemoglobin, ERS, fibrinogen, total cholesterol, triglycerides, insulin, glucose, (and HOMA Index), interleukin-6, TNFα, IL-10, TGF1, IGF-1, adiponectin, lectin, Homocysteine, folic acid and vitamin B12, calprotectin
2 months
Oxidative stress: plasma total antioxidant capacity by TEAA (Trolox Equivalent Antioxidant Activity), glutathione level, the superoxide dismutase, the glutathione peroxidase, the glutathione reductase and the catalase activities
2 months
Gut microbiota: expression of 16S ribosomal RNA in bacterial groups from faeces. Ratio between lactobacilli and clostridia bacteria. Real time PCR and PCR DGGE
2 months
Quality of life: SF-36, GHQ, and daily VAS, ECOG performance status, IADL, Speilbeger Anxiety Scale, CES-D scale
2 months
Physical performance status (SPPB), muscle function (hand-grip dynamometry), and physical activity level (IPAQ)
2 months
- +1 more secondary outcomes
Study Arms (4)
Diet advices
ACTIVE COMPARATORwill receive the Optimal Diet for Elderly
Diet advices + VSL-3
EXPERIMENTALwill receive the Optimal Diet for Elderly + VSL#3® probiotic blend
Diet advices + 5203-L
EXPERIMENTALwill receive the Optimal Diet for Elderly + AISA-5203-L fruit extracted terpene
Diet advices + Argan oil
EXPERIMENTALwill receive the Optimal Diet for Elderly + Argan oil
Interventions
Product should be administrated orally, 2 capsules b.i.d. on an empty stomach (at least 30 min. before lunch and dinner) with a glass of water
Product should be administrated orally, the dosage depending from the body weight of the subject enrolled in the study as already stated : 1-2 pills three times a day with a meal and a large glass of water
Product should be administrated orally, 25 ml once daily or during the day with a meal (bread, salad …) and a large glass of water
a dietician will train each subject (or the caregiver) to use the personalized diet on web platform.
Eligibility Criteria
You may qualify if:
- Age: from 65 to 85 years
- Body Mass Index: 22-30 kg/m2
- ECOG Performance status: WHO performance score 0 to 2
- Absence of known diseases and/or abnormalities of haematological parameters (haematological, inflammatory, metabolic, hepatic and renal diseases)
- The subjects must be able to comply with management of nutraceutical products and with scheduled follow-up
- The subjects must be able to use the computer and to access to the web, by themselves or with the help of a caregiver
You may not qualify if:
- History of significant neurologic or psychiatric disorders including dementia, seizures, bipolar disorder
- Geriatric anorexia \[less than 2 full meals per day and /or less than one serving of dairy products (milk, cheese, yogurt) per day or two or more servings of legumes or eggs per week or one serving of meat, fish or poultry every day\]
- Weight loss \> 5% in the last month
- Previous antibiotic treatment within 4 months
- Active infection requiring per OS or IV antibiotics, including active tuberculosis, known and declared HIV, HCV
- Constipation and/or abdominal pain/discomfort that require dietary supplements or medical therapy
- Gastric disease that requires medical therapy (e.g. gastric secretion inhibitory drugs)
- Chronic inflammatory bowel disease (Crohn's disease or ulcerative colitis, diverticulosis, diverticulitis)
- Diabetes mellitus
- Dislipidemia and/or any metabolic disease that requires medical or dietetic treatment
- Myocardial infarction within 6 months prior to study entry, congestive heart disease, uncontrolled cardiac insufficiency, and any current grade 3 or 4 cardio-vascular disorder despite treatment
- Current history of neoplasm except for curatively treated non melanoma skin cancer or in situ carcinoma of the cervix and except for other cancer curatively treated and with no evidence of disease for at least 5 years
- Other sever underlying medical conditions, which could impair the ability of the patient to participate in the study
- Previous (within 15 days) or concomitant treatment that modifies intestinal absorption (e.g. metformine, acarbose in diabetic treatment…)
- Probiotics, prebiotics or simbiotics (yogurt or another functional foods) intake in the last 3 weeks
- +6 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pôle de gerontology Clinique Hôpital Xavier Arnozan , University Hospital, Bordeaux
Pessac, 33600, France
Related Publications (6)
Franceschi C, Valensin S, Bonafe M, Paolisso G, Yashin AI, Monti D, De Benedictis G. The network and the remodeling theories of aging: historical background and new perspectives. Exp Gerontol. 2000 Sep;35(6-7):879-96. doi: 10.1016/s0531-5565(00)00172-8.
PMID: 11053678BACKGROUNDWener MH, Daum PR, McQuillan GM. The influence of age, sex, and race on the upper reference limit of serum C-reactive protein concentration. J Rheumatol. 2000 Oct;27(10):2351-9.
PMID: 11036829BACKGROUNDMendall MA, Patel P, Ballam L, Strachan D, Northfield TC. C reactive protein and its relation to cardiovascular risk factors: a population based cross sectional study. BMJ. 1996 Apr 27;312(7038):1061-5. doi: 10.1136/bmj.312.7038.1061.
PMID: 8616412BACKGROUNDDevaraj S, O'Keefe G, Jialal I. Defining the proinflammatory phenotype using high sensitive C-reactive protein levels as the biomarker. J Clin Endocrinol Metab. 2005 Aug;90(8):4549-54. doi: 10.1210/jc.2005-0069. Epub 2005 May 17.
PMID: 15899961BACKGROUNDOstan R, Bene MC, Spazzafumo L, Pinto A, Donini LM, Pryen F, Charrouf Z, Valentini L, Lochs H, Bourdel-Marchasson I, Blanc-Bisson C, Buccolini F, Brigidi P, Franceschi C, d'Alessio PA. Impact of diet and nutraceutical supplementation on inflammation in elderly people. Results from the RISTOMED study, an open-label randomized control trial. Clin Nutr. 2016 Aug;35(4):812-8. doi: 10.1016/j.clnu.2015.06.010. Epub 2015 Jul 15.
PMID: 26249791DERIVEDValentini L, Pinto A, Bourdel-Marchasson I, Ostan R, Brigidi P, Turroni S, Hrelia S, Hrelia P, Bereswill S, Fischer A, Leoncini E, Malaguti M, Blanc-Bisson C, Durrieu J, Spazzafumo L, Buccolini F, Pryen F, Donini LM, Franceschi C, Lochs H. Impact of personalized diet and probiotic supplementation on inflammation, nutritional parameters and intestinal microbiota - The "RISTOMED project": Randomized controlled trial in healthy older people. Clin Nutr. 2015 Aug;34(4):593-602. doi: 10.1016/j.clnu.2014.09.023. Epub 2014 Oct 8.
PMID: 25453395DERIVED
MeSH Terms
Interventions
Study Officials
- PRINCIPAL INVESTIGATOR
Isabelle BOURDEL-MARCHASSON, Professor
University Hospital, Bordeaux
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
February 15, 2010
First Posted
February 17, 2010
Study Start
March 1, 2010
Primary Completion
April 1, 2011
Study Completion
April 1, 2011
Last Updated
June 1, 2011
Record last verified: 2011-05