- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT02109588
Early Prevention of Childhood Obesity: an Active Pregnancy
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Studietype
Inschrijving (Verwacht)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Madrid, Spanje, 28040
- Werving
- Universidad Politecnica de Madrid
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Contact:
- María Perales Santaella, PhD student
- Telefoonnummer: 913364081
- E-mail: m.perales.santaella@gmail.com
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Contact:
- Ruben Barakat, PhD
- Telefoonnummer: 913364120
- E-mail: barakatruben@gmail.com
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Being healthy and able to exercise following American College of Obstetricians and Gynecologists (ACOG) guidelines
- Being able to communicate in spanish
- Giving birth at Hospital Universitario de Torrejón, hospital Universitario de Puerta de Hierro and Hospital Universitario Severo Ochoa (Madrid).
Exclusion Criteria:
- Multiparity
- Obstetrician complications
- Being interested in the study after 16 weeks
- Not being regular in physical exercise program
- Younger than 18 years old
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Geen tussenkomst: Controle
Sedentaire zwangere vrouwen
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Experimenteel: Exercise group
Supervised physical conditioning program of three 55-60 minute sessions per week during whole pregnancy (from week 9 to 38). Each session consists of 25-30 minutes of cardiovascular exercise,10 minutes of specific exercises (strength and balance exercises), and 10 minutes of pelvic floor muscles training Aerobic activity was prescribed at light to moderate intensity, aiming for 55-60% of heart rate reserve. All subjects wore a heart rate (HR) monitor (Polar FT7) during the training sessions to ensure that exercise intensity was light to moderate |
Supervised physical conditioning program of three 55-60 minute sessions per week during whole pregnancy (from week 9 to 38). Each session consists of 25-30 minutes of cardiovascular exercise,10 minutes of specific exercises (strength and balance exercises), and 10 minutes of pelvic floor muscles training Aerobic activity was prescribed at light to moderate intensity, aiming for 55-60% of heart rate reserve. All subjects wore a heart rate (HR) monitor (Polar FT7) during the training sessions to ensure that exercise intensity was light to moderate |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Body mass index of the offsprings
Tijdsspanne: 0-24 postpartum months
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Body mass index was measured several times from 0 to 24 months
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0-24 postpartum months
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Fetus body composition
Tijdsspanne: 0-24 postpartum months
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Fetus body composition (percentage of fat) was measured several times from 0 to 24 months
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0-24 postpartum months
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Change from baseline in Maternal gestational weight gain
Tijdsspanne: 40-42 weeks of gestation
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Maternal weight gain during pregnancy
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40-42 weeks of gestation
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Changes in Baby motor development
Tijdsspanne: 0-24 postpartum months
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Baby motor development was measured after delivery
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0-24 postpartum months
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Recovery time to pre-gestational weight
Tijdsspanne: 6-12 postpartum months
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The time needed to recovery the pre-gestational weight was assessed.
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6-12 postpartum months
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Glycemia level of the offsprings
Tijdsspanne: 0-24 postpartum months
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Glycemia level of the offsprings was measured until 24 months
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0-24 postpartum months
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Postpartum depression
Tijdsspanne: 0-12 postpartum months
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The level of maternal depression was measured after delivery
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0-12 postpartum months
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Change from baseline in Body image satisfaction
Tijdsspanne: up to 36 weeks
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Body image satisfaction was measured during and after pregnancy
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up to 36 weeks
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Changes from baseline in maternal quality of life
Tijdsspanne: up to 36 weeks
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Maternal quality of life was measured during and after pregnancy
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up to 36 weeks
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Placenta measurements
Tijdsspanne: At delivery
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Placenta measurements were collected at labor
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At delivery
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Maternal outcomes
Tijdsspanne: At delivery
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Type of labor, stage of labor and some other maternal variables were measured at delivery
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At delivery
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Control of physical activity
Tijdsspanne: up to 10 weeks
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Control the level of physical activity during and after pregnancy
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up to 10 weeks
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Changes from delivery in Health of the offspring
Tijdsspanne: 0-24 postpartum months
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Health of the baby included the measurement of other variables such as blood pressure and cholesterol of the offsprings until 24 months
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0-24 postpartum months
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Fetus outcomes
Tijdsspanne: At delivery
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Fetus outcomes were measured at delivery: Apgar score, PH umbilical cord, size and height of the baby, head circumference
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At delivery
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Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Schatting)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- Prevention childhood obesity
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
Klinische onderzoeken op A supervised physical exercise program
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Microclinic InternationalRoyal Health Awareness Society (RHAS); Jordanian Ministry of Health (MoH)VoltooidHyperglykemie | Hypertensie | Obesitas | Diabetes mellitus, type 2 | Suikerziekte | Suikerziekte | Lichaamsgewicht | Gewichtsverlies | Bloeddruk | Gewichtstoename | Sociaal gedrag | Gewicht, lichaam | Glucose, hoog bloed | Levensstijl, gezond | Gewichtsverandering, lichaam | Gedrag, gezondheid | Risicovermindering van levensstijl en andere voorwaardenJordanië