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Combined Resistance and Aerobic Exercise Training on Obesity in Adolescent Girls

30. oktober 2020 opdateret af: Won-mok son, Pusan National University

Effectiveness of Combined Resistance and Aerobic Exercise Training on Obesity in Adolescent Girls

The purpose of the study was to observe therapeutic effects of combined resistance and aerobic exercise training (CRAE) on hyperinsulemia in obese adolescent girls. Forty obese adolescent girls (14±1 years) participated in this study. The participants were randomly separated into two groups; no-exercise group (n=20) and exercise group (n=20). The exercise group performed 12 weeks of CRAE.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

40

Fase

  • Ikke anvendelig

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

14 år til 16 år (Barn)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Kvinde

Beskrivelse

Inclusion Criteria:

  • Obese with Hyperinsulinemia
  • Obese with Abdominal obesity

Exclusion Criteria:

  • Hypertension
  • Pregnancy
  • Chronic diseases
  • Weight loss diet within the last 6 months

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Sundhedstjenesteforskning
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: No Exercise (CON)
Twenty obese adolescent girls. This arm did not perform any exercise training for 12 weeks. Caloric intake: 1921.7 kcal/day
Eksperimentel: Exercise (EX)
Twenty obese adolescent girls. This arm performed combined exercise training 5 times a week for 12 weeks. Caloric intake: 1921.7 kcal/day
Adfærdsmæssigt: Combined Exercise Training
The combined exercise training were consisted with 5 minutes of warm-up, 20 minutes of resistant band exercises (Upper: seated rows, biceps curl, shoulder flexion, elbow flexion, pushup; Lower: hip flexion, hip extension, calf raise, leg press, squat), 30 minutes of treadmill walking, and 5 minutes of cool-down. Intensity of the training was gradually increased from 40-50% heart rate reserve in 1-4 weeks to 60-70% HRR in 9-12 weeks.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Height in Meters
Tidsramme: 12 weeks
Height was measured before and after 12 weeks.
12 weeks
Weight in Kilograms
Tidsramme: 12 weeks
Weight was measured before and after 12 weeks.
12 weeks
BMI in Weight (Kilograms)/Height (Meters)^2
Tidsramme: 12 weeks
BMI was calculated with weight and height before and after 12 weeks.
12 weeks
Body Fat in Percents
Tidsramme: 12 weeks
Body fat was measured before and after 12 weeks.
12 weeks
Lean Body Mass in Percents
Tidsramme: 12 weeks
Lean body mass was measured before and after 12 weeks.
12 weeks
Waist Circumference in Centimeters
Tidsramme: 12 weeks
Waist circumference was measured before and after 12 weeks.
12 weeks
Glucose Levels in Millimole Per Liter
Tidsramme: 12 weeks
Glucose levels were measured before and after 12 weeks.
12 weeks
Insulin Levels in Micro Unit Per Milliliter
Tidsramme: 12 weeks
Insulin levels were measured before and after 12 weeks.
12 weeks
Homeostasis Model Assessment of Insulin Resistance (HOMA-IR)
Tidsramme: 12 weeks
Homeostasis model assessment of Insulin Resistance (HOMA-IR) was calculated before and after 12 weeks
12 weeks
Leptin Levels in Nano Grams Per Milliliter
Tidsramme: 12 weeks
Leptin levels were measured before and after 12 weeks.
12 weeks
Adiponectin Levels in Micro Grams Per Milliliter
Tidsramme: 12 weeks
Adiponectin levels were measured before and after the training.
12 weeks

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Volume of Maximal Oxygen Consumption (VO2max)
Tidsramme: 12 weeks
Volume of maximal oxygen consumption (VO2max) was determined using a maximal treadmill test before and after 12 weeks.
12 weeks
Arterial Stiffness
Tidsramme: 12 weeks
Brachial-ankle Pulse Wave Velocity (m/s) was measured using applanation tonometry before and after 12 weeks.
12 weeks
Systolic Blood Pressure
Tidsramme: 12 weeks
Systolic blood pressure was measured before and after 12 weeks.
12 weeks
Diastolic Blood Pressure
Tidsramme: 12 weeks
Diastolic blood pressure was measured before and after 12 weeks.
12 weeks
Maximal Heart Rate
Tidsramme: 12 weeks
12 weeks

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Pusan National University

Samarbejdspartnere

Dong-Eui University

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

3. marts 2011

Primær færdiggørelse (Faktiske)

3. juni 2011

Studieafslutning (Faktiske)

5. juni 2011

Datoer for studieregistrering

Først indsendt

17. marts 2017

Først indsendt, der opfyldte QC-kriterier

24. marts 2017

Først opslået (Faktiske)

30. marts 2017

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

3. november 2020

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

30. oktober 2020

Sidst verificeret

1. oktober 2020

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • UNOmaha7

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Combined Exercise Training

Søg i lignende forsøg

Sponsorer og samarbejdspartnere

Medicinske tilstande

Narkotikainterventioner

CROs by country

CROs in Mongolia

Betingelser

Sjældne sygdomme

Narkotikainterventioner

Kosttilskud

Sponsor / samarbejdspartnere

Placeringer

Abonner