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Exercise Training in Pregnancy for Obese Mothers

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

調査の概要

状態

完了

条件

介入・治療

詳細な説明

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.

研究の種類

介入

入学 (実際)

91

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Trondheim、ノルウェー、7489
        • Norwegian University of Science and Technology

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

女性

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的: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
Exercise training at the hospital
他の名前:
  • トレーニング
介入なし:Control
Usual care as provided by the health services in Norway. The investigators will not advice the women to be inactive

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Weight gain during pregnancy
時間枠:From 14 weeks pregnancy to delivery
Measured in kg
From 14 weeks pregnancy to delivery

二次結果の測定

結果測定
メジャーの説明
時間枠
Fasting glucose
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Blood samples to determine the fasting glucose after an overnight fast (>10 hours)
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Glucose tolerance
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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.
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Insulin resistance
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Homeostasis model assessment (HOMA-IR)
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Body composition
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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.
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Blood markers for cardiovascular disease
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Inflammation markers, cytokines (leptin, resistin, adiponectin, tnf-alfa). Blood will be collected and stored for later analyses.
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Lumbopelvic pain
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Clinical assessment (active straight leg raising, pelvic provocation test), and validated questionnaire.
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Urin- and fecal incontinence
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
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
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Quality of life
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Validated questionnaire
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Sleep
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Epworth sleepiness scale
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Physical activity
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Level of physical activity will be assessed by activity registration (armbands) and by validated questionnaires
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Diet
時間枠:From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Validated questionnaire: Norkost
From 14 weeks pregnancy to 38 weeks pregnancy and also at 3 months postpartum
Offspring birth weight, length and head circumference
時間枠:At delivery
As recorded by the hospital
At delivery
Delivery complications
時間枠:At delivery
Vaginal or caesarean delivery, and recorded complications during the delivery
At delivery
Markers of inflammation and metabolism in cord blood
時間枠:At delivery
Cord blood will be sampled and stored for later analysis of relevant markers of inflammation and metabolism (including resistin, leptin, adiponectin)
At delivery

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2010年9月1日

一次修了 (実際)

2015年6月1日

研究の完了 (実際)

2016年6月1日

試験登録日

最初に提出

2010年9月6日

QC基準を満たした最初の提出物

2010年11月17日

最初の投稿 (見積もり)

2010年11月18日

学習記録の更新

投稿された最後の更新 (実際)

2020年1月28日

QC基準を満たした最後の更新が送信されました

2020年1月24日

最終確認日

2018年6月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • ETiP-Ob

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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