- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02347696
Diet and Physical Activity on NAFLD and Erytrocyte Membrane Lipid Profile.
Effect of Two Programs of Physical Activity of Different Intensity, Mediterranean Diet and the Combination of Both on NAFLD and Erytrocyte Membrane Lipid Profile.
Studieoversikt
Status
Forhold
Detaljert beskrivelse
The surveys conducted on the populations of Castellana Grotte and Putignano (Bari, Italy) evidenced that Non-Alcoholic Fatty liver Disease (NAFLD) reaches a prevalence of 30%, especially among aged and male individuals. Being a crucial outcome of several metabolic alterations, it becomes imperative for Public Health to adopt strategies aimed to control the factors responsible for NAFLD onset.
The objective of this study is to evaluate the effect of two programs of different intensity level of physical activity, of low glycemic index Mediterranean Diet and of the interaction of both, on NAFLD score and on the lipid composition of the erythrocyte membrane.
Study participants responding to the inclusion criteria of this trial will be chosen both in the hospital setting and in the general practitioners' clinics. At the enrollement, anthropometric and biochemical variables will be measured, as well as bioimpedenziometric and calorimetric parameters; participants will also undergo Fibroscan-CAP to measure the outcome and will be asked about their medical history and life-style. Subjects will be randomized to the different arms of the trial and be followed-up at the end of the sixth and the twelfth week of enrollement.
All data will be statistically analysed by applying the Chi-Square test and t-test for discrete and continuous variables, respectively. As it deals with the analysis of data repeatedly measured on the same subject, the Generalized Estimating Equation (GEE) will be applied to evaluate the effect of the intervention on the outcomes.
Studietype
Registrering (Forventet)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Alberto R Osella, MD, PhD
- Telefonnummer: 00390804994655
- E-post: arosella@irccsdebellis.it
Studiesteder
-
-
BA
-
Castellana Grotte, BA, Italia, 70013
- Rekruttering
- Laboratory of Epidemiology and Biostatistics-IRCCS Saverio de Bellis
-
Ta kontakt med:
- Isabella Franco, BSc
- Telefonnummer: 00390804994650
- E-post: isabella.franco@irccsdebellis.it
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- BMI ≥ 25.0
- Moderate or severe NAFLD
- 30 < age <60
Exclusion Criteria:
- Overt cardiovascular disease and revascularization procedures;
- Stroke;
- Clinical peripheral artery disease;
- Type-2 Diabetes Mellitus (current treatment with insulin or oral hypoglycemic drugs, fasting glucose >126 mg/dl, or casual glucose >200 mg/dl);
- Severe medical condition that may impair the person to participate in a nutritional intervention study;
- Impossibility to follow Mediterranean Diet for religious or other reasons.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Annen: Control
The subjects will follow a diet based on INRAN guidelines without doing any physical activity.
|
Subjects will follow a diet based on INRAN guidelines without doing any physical activity.
|
Annen: LGIMD
The subjects will follow a Low Glycemic Index Mediterranean Diet without doing any physical activity.
|
Subjects will follow a Low Glycemic Index Mediterranean Diet (LGIMD) without doing any physical activity.
|
Annen: Endurance Activity (EA)
The subjects will follow a program of endurance (aerobic) activity (EA) without following a specific diet.
|
Subject will follow a program of endurance activity as follows: Frequency: 3 times/week Duration: 60 minutes Intensity:
|
Annen: EA+Resistance Training (RT)
The subjects will follow a program of endurance activity (EA) and resistance training (RT) without following a specific diet.
|
Subject will follow a program of endurance activity as follows: Frequency: 3 times/week Duration: 60 minutes Intensity (for Endurance activity):
Resistance activity: Muscolation: Training of the bigger muscle groups (chest, shoulders, arms, abdomen, back, glutes and legs);
|
Annen: LGIMD+EA
The subjects will follow a Low Glycemic Index Mediterranean Diet (LGIMD) togheter with a program of endurance activity (EA).
|
Subjects will follow a Low Glycemic Index Mediterranean Diet together with a program of endurance activity.
|
Annen: LGIMD+EA/RT
The subjects will follow a Low Glycemic Index Mediterranean Diet (LGIMD) togheter with a program of endurance activity (EA) and resistance training (RT).
|
Subjects will follow a Low Glycemic Index Mediterranean Diet together with a program of both endurance activity and resistance training.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Non-Alcoholic Fatty liver Disease (NAFLD) score
Tidsramme: up to 12 weeks
|
NAFLD score will be built with Fobroscan-CAP
|
up to 12 weeks
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Lipid composition of erythrocyte membrane
Tidsramme: 6 and 12 weeks
|
6 and 12 weeks
|
Sierical lipid profile
Tidsramme: 6 and 12 weeks
|
6 and 12 weeks
|
Samarbeidspartnere og etterforskere
Etterforskere
- Hovedetterforsker: Alberto R Osella, MD, PhD, IRCCS "Saverio de Bellis"
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- NUTRIATT
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
Kliniske studier på NAFLD
-
Bambino Gesù Hospital and Research InstituteFullført
-
Ziv HospitalUkjent
-
University of AthensLaikο General Hospital, AthensHar ikke rekruttert ennå
-
Milton S. Hershey Medical CenterRekruttering
-
Second Affiliated Hospital, School of Medicine,...Har ikke rekruttert ennåNAFLD | Kostholdsvane
-
University of OxfordRekrutteringNAFLD | Næringsstoff; OverskuddStorbritannia
-
Enanta Pharmaceuticals, IncPharmaceutical Research AssociatesFullført
-
Ann & Robert H Lurie Children's Hospital of ChicagoHar ikke rekruttert ennåNAFLD | Ikke-alkoholisk fettleversykdom | Pediatrisk NAFLDForente stater
-
University of California, San FranciscoNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)RekrutteringHiv | NAFLD | NAFLD-HIVForente stater
Kliniske studier på Control
-
Indiana UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development...RekrutteringPrevensjon | Utnyttelse av helsevesenet | PrevensjonsbrukForente stater
-
Essilor InternationalAktiv, ikke rekrutterende
-
Singapore General HospitalDuke-NUS Graduate Medical SchoolUkjentKardiovaskulære sykdommer | Hypertensjon | Kroniske nyresykdommerSingapore
-
University of UtahJohns Hopkins University; Arizona State University; National Multiple Sclerosis...FullførtMultippel sklerose | Svimmelhet | Svimmelhet | FallskadeForente stater
-
National Taiwan University HospitalFullførtSykehusinnleggelsesrate | Dødelighetsrate | Funksjonell gjenoppretting | Venstre ventrikkel ejeksjonsfraksjon | NT-pro BNPTaiwan
-
Summa Health SystemFullførtHjertefeilForente stater
-
Staffordshire UniversityAvsluttetOsteoporose, postmenopausalStorbritannia
-
University of California, San FranciscoUniversity of California, BerkeleyFullført
-
Texas Woman's UniversityFullførtAutismespektrumforstyrrelse
-
Istanbul Medipol University HospitalAktiv, ikke rekrutterende