Exercise Training in Pregnancy for Obese Mothers
24 de enero de 2020 actualizado por: 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
Descripción general del estudio
Descripción detallada
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.
Tipo de estudio
Intervencionista
Inscripción (Actual)
91
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Trondheim, Noruega, 7489
- Norwegian University of Science and Technology
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
18 años y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Femenino
Descripción
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 de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: 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
Otros nombres:
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Sin intervención: 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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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Weight gain during pregnancy
Periodo de tiempo: 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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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Fasting glucose
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: At delivery
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As recorded by the hospital
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At delivery
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Delivery complications
Periodo de tiempo: 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
Periodo de tiempo: 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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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
- 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.
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio
1 de septiembre de 2010
Finalización primaria (Actual)
1 de junio de 2015
Finalización del estudio (Actual)
1 de junio de 2016
Fechas de registro del estudio
Enviado por primera vez
6 de septiembre de 2010
Primero enviado que cumplió con los criterios de control de calidad
17 de noviembre de 2010
Publicado por primera vez (Estimar)
18 de noviembre de 2010
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
28 de enero de 2020
Última actualización enviada que cumplió con los criterios de control de calidad
24 de enero de 2020
Última verificación
1 de junio de 2018
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- ETiP-Ob
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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