Exercise Training in Pregnancy for Obese Mothers
24 janvier 2020 mis à jour par: Norwegian University of Science and Technology
Exercise Training in Pregnancy. Good for the Mother - Good for the Child?
Observational studies demonstrate that overweight in pregnancy is a risk factor for adverse pregnancy outcomes as fetal macrosomia, prolonged labor, low Apgar score, shoulder dystocia, nerve plexus injuries, increased proportion of instrumental deliveries and perineal ruptures. There is a 2.6 fold risk for gestational diabetes mellitus (fourfold in morbidly obese women) and a recent study has shown that fetuses of obese mothers develop insulin resistance in uterus.
Main aims of this study are to assess if regular exercise in pregnancy among obese women can prevent or influence weight gain; impaired cardiac function in mother and fetus/newborn; impaired vascular function in mother; insulin resistance/sensitivity; body composition in mother and offspring; lumbopelvic pain; urinary and/or fecal incontinence; prolonged labor
Aperçu de l'étude
Description détaillée
Women with a self-reported pre-pregnancy BMI of 28 or more will be eligible for our study. Woman are eligible if they are 18 years or older, with a singleton live fetus at an early (week 12-14) ultrasound scan. Exclusion criteria are pregnancy complications with high risk for preterm labour or diseases that could interfere with participation.
Primary outcome measure is weight increase based on weight measured at 14 weeks and immediately before labour. Assessments are done at baseline at 14 (12-18) weeks of pregnancy, and again in week 38, as well as 3 months postpartum. Some measurements are also done at other points in time. The maternal secondary outcome measurements include fasting glucose, glucose tolerance assessed by 2-h, 75 mg per-oral glucose tolerance test, insulin resistance assessed by HOMA-IR, weight, height, body composition estimated by skinfold measurements in pregnancy and by dual energy x-ray absorptiometry postpartum, blood markers, lumbopelvic pain, urin- and fecal incontinence, quality of life, psychological wellbeing, depression, and diet.
Type d'étude
Interventionnel
Inscription (Réel)
91
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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Trondheim, Norvège, 7489
- Norwegian University of Science and Technology
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Femelle
La description
Inclusion Criteria:
- Pre-pregnancy body mass index of 28 or more
- 18 years or more
- singleton live fetus at the routine ultrasound scan
Exclusion Criteria:
- high risk for preterm labor or diseases that could interfere with participation
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
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Expérimental: Exercise training
Supervised exercise training at the hospital during pregnancy: the women will attend at least 2 weekly sessions consisting of aerobic exercise (walking on treadmills), strength training (for upper body, back, abdomen and legs) as well as pelvic floor muscle exercises.
Each session is 60 minutes and lead by a physiotherapist or experienced exercise physiologist.
The women will also go through motivational interviewing sessions throughout the intervention period and are encouraged to do home exercise training in addition to the exercise at the hospital
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Exercise training at the hospital
Autres noms:
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Aucune intervention: Control
Usual care as provided by the health services in Norway.
The investigators will not advice the women to be inactive
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
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Weight gain during pregnancy
Délai: From 14 weeks pregnancy to delivery
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Measured in kg
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From 14 weeks pregnancy to delivery
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Fasting glucose
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Blood samples to determine the fasting glucose after an overnight fast (>10 hours)
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Glucose tolerance
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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2 hour 75 mg per-oral glucose tolerance test.
Gestational diabetes is diagnosed as fasting glucose = or > 6.9 mmol/L or 2h concentration = or > 7.8 mmol/L.
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Insulin resistance
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Homeostasis model assessment (HOMA-IR)
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Body composition
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Skinfold measurements, done by an experienced investigator using Harpenden kaliper.
At the 3 months postpartum testing, also dual energy x-ray absorptiometry (DEXA scan) will be used.
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Blood markers for cardiovascular disease
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Inflammation markers, cytokines (leptin, resistin, adiponectin, tnf-alfa).
Blood will be collected and stored for later analyses.
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Lumbopelvic pain
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Clinical assessment (active straight leg raising, pelvic provocation test), and validated questionnaire.
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Urin- and fecal incontinence
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Pelvic floor muscle function will be assessed by clinical assessment and by 2D and 3D ultrasound.
The prevalence and severity of urin- and fecal incontinence will also be assessed by a validated questionnaire
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Quality of life
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Validated questionnaire
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Sleep
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Epworth sleepiness scale
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Physical activity
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Level of physical activity will be assessed by activity registration (armbands) and by validated questionnaires
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Diet
Délai: From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Validated questionnaire: Norkost
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From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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Offspring birth weight, length and head circumference
Délai: At delivery
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As recorded by the hospital
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At delivery
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Delivery complications
Délai: At delivery
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Vaginal or caesarean delivery, and recorded complications during the delivery
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At delivery
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Markers of inflammation and metabolism in cord blood
Délai: At delivery
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Cord blood will be sampled and stored for later analysis of relevant markers of inflammation and metabolism (including resistin, leptin, adiponectin)
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At delivery
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Publications générales
- Woodley SJ, Lawrenson P, Boyle R, Cody JD, Morkved S, Kernohan A, Hay-Smith EJC. Pelvic floor muscle training for preventing and treating urinary and faecal incontinence in antenatal and postnatal women. Cochrane Database Syst Rev. 2020 May 6;5(5):CD007471. doi: 10.1002/14651858.CD007471.pub4.
- Garnaes KK, Morkved S, Salvesen O, Moholdt T. Exercise Training and Weight Gain in Obese Pregnant Women: A Randomized Controlled Trial (ETIP Trial). PLoS Med. 2016 Jul 26;13(7):e1002079. doi: 10.1371/journal.pmed.1002079. eCollection 2016 Jul.
- Garnaes KK, Nyrnes SA, Salvesen KA, Salvesen O, Morkved S, Moholdt T. Effect of supervised exercise training during pregnancy on neonatal and maternal outcomes among overweight and obese women. Secondary analyses of the ETIP trial: A randomised controlled trial. PLoS One. 2017 Mar 21;12(3):e0173937. doi: 10.1371/journal.pone.0173937. eCollection 2017.
- Garnaes KK, Morkved S, Salvesen KA, Salvesen O, Moholdt T. Exercise training during pregnancy reduces circulating insulin levels in overweight/obese women postpartum: secondary analysis of a randomised controlled trial (the ETIP trial). BMC Pregnancy Childbirth. 2018 Jan 8;18(1):18. doi: 10.1186/s12884-017-1653-5.
- Nyrnes SA, Garnaes KK, Salvesen O, Timilsina AS, Moholdt T, Ingul CB. Cardiac function in newborns of obese women and the effect of exercise during pregnancy. A randomized controlled trial. PLoS One. 2018 Jun 1;13(6):e0197334. doi: 10.1371/journal.pone.0197334. eCollection 2018.
- Garnaes KK, Helvik AS, Stafne SN, Morkved S, Salvesen K, Salvesen O, Moholdt T. Effects of supervised exercise training during pregnancy on psychological well-being among overweight and obese women: secondary analyses of the ETIP-trial, a randomised controlled trial. BMJ Open. 2019 Nov 21;9(11):e028252. doi: 10.1136/bmjopen-2018-028252.
- Ingul CB, Loras L, Tegnander E, Eik-Nes SH, Brantberg A. Maternal obesity affects fetal myocardial function as early as in the first trimester. Ultrasound Obstet Gynecol. 2016 Apr;47(4):433-42. doi: 10.1002/uog.14841. Epub 2016 Mar 14.
- Moholdt TT, Salvesen K, Ingul CB, Vik T, Oken E, Morkved S. Exercise Training in Pregnancy for obese women (ETIP): study protocol for a randomised controlled trial. Trials. 2011 Jun 17;12:154. doi: 10.1186/1745-6215-12-154.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude
1 septembre 2010
Achèvement primaire (Réel)
1 juin 2015
Achèvement de l'étude (Réel)
1 juin 2016
Dates d'inscription aux études
Première soumission
6 septembre 2010
Première soumission répondant aux critères de contrôle qualité
17 novembre 2010
Première publication (Estimation)
18 novembre 2010
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
28 janvier 2020
Dernière mise à jour soumise répondant aux critères de contrôle qualité
24 janvier 2020
Dernière vérification
1 juin 2018
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- ETiP-Ob
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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