- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05124847
Behandling af pædiatrisk fedme (TREPO)
Tidsbegrænset spisning som en behandling for pædiatrisk fedme
Studieoversigt
Status
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Málaga, Spanien, 29011
- Hospital Regional Universitario de Málaga. Hospital Materno-Infantil.
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Beskrivelse
Inklusionskriterier:
- Alder mellem 10 og 15 ved studiestart.
Fedme defineret i henhold til kriterierne fra Verdenssundhedsorganisationen (BMI≥p95) og mindst én af følgende tilstande:
2.1. Hepatisk steatose bekræftet ved abdominal ultralyd i de foregående 12 måneder.
2.2. Triglycerider > 150 mg/dl, bekræftet ved analytisk bestemmelse i de 4 uger før studiets start.
2.3. HDL-kolesterol <40 mg/dl, bekræftet ved analytisk bestemmelse i de 4 uger før studiets start.
2.4. LDL-kolesterol > 135 mg/dl, bekræftet ved analytisk bestemmelse i de 4 uger før studiets start.
2.5. Insulinresistens, bestemt ved forhøjet HOMA-IR bekræftet ved analytisk bestemmelse i de 4 uger før studiets start.
- Vaneligt spisevindue lig med eller større end 13 timer, med en svarprocent på over 85 %. Vinduet for vanespisning vil blive bestemt ved selvregistrering under screeningsprocessen. Deltagerne skal registrere det sædvanlige spisevindue korrekt i mindst 12 af de 14 dage, som selvregistrering vil blive anmodet om, og det skal være lig med eller større end 13 timer mindst 6 dage om ugen.
- Rapportering at have opretholdt en stabil vægt- og højdestatus i løbet af de sidste to måneder (ændringer på mindre end 2 point i BMI (kg/m2)).
- Aftale om at deltage i alle faser og procedurer af undersøgelsen.
Ekskluderingskriterier:
- At blive diagnosticeret med en endokrin lidelse, for eksempel diabetes mellitus under behandling med insulin eller orale antidiabetika, skjoldbruskkirtelsygdom, hypercortisolisme, medfødt binyrehyperplasi.
- At blive diagnosticeret med en kronisk fordøjelsessygdom, reumatologisk, neurologisk, kardiologisk, pneumologisk, autoimmun eller infektionssygdom, der påvirker energistofskiftet.
- At have gennemgået et kirurgisk indgreb, der kronisk skifter fordøjelses- eller metabolisk funktion.
- Hyperkolesterolæmi, der kræver farmakologisk behandling i henhold til ekspertkonsensus fra European Society of Arteriosclerosis specifikt for børn.
- Serum triglyceridkoncentration > 500 mg/dl.
- Systoliske eller diastoliske blodtryksværdier lig med eller større end den specifikke 95. percentil for alder, sjette og højde ved 3 forskellige lejligheder [42].
- Hypertransaminasæmi > 200 IE/L (5 gange højere end den øvre normalværdi i laboratoriet), hvilket ville gøre det nødvendigt at udelukke andre årsager til leversygdom.
- At blive diagnosticeret med en spiseforstyrrelse eller være i risiko for at udvikle disse lidelser, bestemt ved hjælp af SCOFF-spørgeskemaet (to eller flere spørgsmål besvaret positivt).
- Præsenterer neurologiske ændringer eller kromosomopatier.
- Indtagelse af lægemidler eller kosttilskud, der sandsynligvis vil ændre energistofskiftet.
- At deltage i en ernæringsintervention eller behandling af enhver art, eller have gjort det inden for de foregående 3 måneder.
- At have et bevisligt personligt eller professionelt forhold til nogen af medlemmerne af efterforskningsteamet.
- Enhver anden betingelse, som efter forskerholdets opfattelse ville kontraindicere deres deltagelse.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: TRE-kontrol
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Deltagerne vil modtage ernæringsundervisningssessioner og vil blive instrueret i at opretholde et indtagsvindue på mindst 13 timer om dagen, helst alle ugens dage og under alle omstændigheder mindst 6 dage om ugen.
En personlig progression vil blive etableret for gradvist at reducere indtagelsesvinduet i løbet af de første 10 dages intervention.
Efter disse første 10 dage vil deltagerne blive ordineret til at begrænse fødeindtagelsen til maksimalt 10 timer om dagen, mindst 5 dage om ugen.
Deltageren kan frit vælge tidspunktet på dagen for at placere indtagsvinduet.
Det vil dog anbefales at undgå at lave det sidste indtag i de 3 timer før sengetid.
Efter 4 ugers intervention vil diætisten opfordre dem til at reducere indtagelsesvinduet til 9 eller 8 timer, hvis de anser det for muligt, og bibeholde dette nye indtagsvindue i løbet af de sidste 4 ugers intervention.
Indtagelsesvinduet kan opretholdes på 10 timer indtil afslutningen af undersøgelsen.
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Eksperimentel: Kontrol-TRE
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Deltagerne vil modtage ernæringsundervisningssessioner og vil blive instrueret i at opretholde et indtagsvindue på mindst 13 timer om dagen, helst alle ugens dage og under alle omstændigheder mindst 6 dage om ugen.
En personlig progression vil blive etableret for gradvist at reducere indtagelsesvinduet i løbet af de første 10 dages intervention.
Efter disse første 10 dage vil deltagerne blive ordineret til at begrænse fødeindtagelsen til maksimalt 10 timer om dagen, mindst 5 dage om ugen.
Deltageren kan frit vælge tidspunktet på dagen for at placere indtagsvinduet.
Det vil dog anbefales at undgå at lave det sidste indtag i de 3 timer før sengetid.
Efter 4 ugers intervention vil diætisten opfordre dem til at reducere indtagelsesvinduet til 9 eller 8 timer, hvis de anser det for muligt, og bibeholde dette nye indtagsvindue i løbet af de sidste 4 ugers intervention.
Indtagelsesvinduet kan opretholdes på 10 timer indtil afslutningen af undersøgelsen.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Længde af spisevindue
Tidsramme: Fra uge 0 til uge 8
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Fra uge 0 til uge 8
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Kropsvægt
Tidsramme: uge 8
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uge 8
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Kropsfedtmasse
Tidsramme: uge 8
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uge 8
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Lipid profil
Tidsramme: uge 8
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uge 8
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HOMA-IR
Tidsramme: uge 8
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uge 8
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Hepatisk steatose
Tidsramme: uge 8
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uge 8
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Carotis intima-media tykkelse
Tidsramme: uge 8
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uge 8
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Kontinuerlig glukoseovervågning
Tidsramme: Fra uge 6 til uge 8
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Fra uge 6 til uge 8
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Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Rafael Martín Masot, MD PhD, Hospital Regional Universitario de Málaga. Hospital Materno-Infantil.
Publikationer og nyttige links
Generelle publikationer
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