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ID

40832

Descrizione

Healthy Lifestyle in Pregnancy; ODM derived from: https://clinicaltrials.gov/show/NCT01585454

collegamento

https://clinicaltrials.gov/show/NCT01585454

Keywords

versioni (1)
  1. 20/05/20 20/05/20 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

20 maggio 2020

DOI

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Creative Commons BY 4.0
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    Eligibility Hperglycemia NCT01585454

    Inglese

    Eligibility Hperglycemia NCT01585454

    1 moduli  
    Criteria
    Descrizione

    Criteria

    1. at least 18 years of age.
    Descrizione

    Age

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    2. receive prenatal care at the nurse midwifery/obstetrics service of pimc and plan to continue receiving such care throughout the pregnancy.
    Descrizione

    Receive Prenatal care

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C1514756
    UMLS CUI [1,2]
    C0033052
    3. are able to have an ogtt prior to 16 weeks gestation (if diabetes was not previously diagnosed). hyperemesis can preclude some pregnant women from successfully completing the ogtt; these women will not be excluded if the fasting blood samples can be obtained. pregnant women with previously diagnosed diabetes are eligible if measures of glycemia (fpg, hba1c, glycated albumin) are completed prior to 16 weeks gestation.
    Descrizione

    Oral Glucose Tolerance Test prior to Gestation weeks | Blood specimen Fasting | Plasma fasting glucose measurement | Hemoglobin A1c measurement | Glycated albumin measurement

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0029161
    UMLS CUI [1,2]
    C0332152
    UMLS CUI [1,3]
    C1135241
    UMLS CUI [2,1]
    C0178913
    UMLS CUI [2,2]
    C0015663
    UMLS CUI [3]
    C0583513
    UMLS CUI [4]
    C0474680
    UMLS CUI [5]
    C0523674
    4. estimated prenatal bmi > 25 kg/m2.
    Descrizione

    Body mass index Prenatal Estimated

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C1305855
    UMLS CUI [1,2]
    C2828394
    UMLS CUI [1,3]
    C0750572
    5. able to commit the time required for the interventions and follow-up.
    Descrizione

    Protocol Compliance

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0525058
    6. able and willing to provide informed consent.
    Descrizione

    Informed Consent

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Descrizione

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    1. contraindication to aerobic or resistance exercise (acog, 2002).
    Descrizione

    Medical contraindication Aerobic Exercise | Medical contraindication Resistance Training

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C1301624
    UMLS CUI [1,2]
    C0001701
    UMLS CUI [2,1]
    C1301624
    UMLS CUI [2,2]
    C0872279
    2. twin or multiple gestation.
    Descrizione

    Twin gestation | Multiple Pregnancy

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0744386
    UMLS CUI [2]
    C0032989
    3. severe anemia, uncontrolled asthma, uncontrolled hypertension, cardiac disease, or any condition that requires follow-up at specialty care clinics outside of pimc (e.g., pregnancies at high risk for maternal or fetal demise).
    Descrizione

    Anemia, severe | Asthma Uncontrolled | Uncontrolled hypertension | Heart Disease | Condition Requirement Specialty care unit | Pregnancy At risk Maternal Death | Pregnancy At risk Fetal Death

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0238644
    UMLS CUI [2,1]
    C0004096
    UMLS CUI [2,2]
    C0205318
    UMLS CUI [3]
    C1868885
    UMLS CUI [4]
    C0018799
    UMLS CUI [5,1]
    C0348080
    UMLS CUI [5,2]
    C1514873
    UMLS CUI [5,3]
    C4034258
    UMLS CUI [6,1]
    C0032961
    UMLS CUI [6,2]
    C1444641
    UMLS CUI [6,3]
    C3494405
    UMLS CUI [7,1]
    C0032961
    UMLS CUI [7,2]
    C1444641
    UMLS CUI [7,3]
    C0015927
    4. any condition that in the opinion of the investigators would interfere with consent, treatment, or follow-up.
    Descrizione

    Condition Interferes with Informed Consent | Condition Interferes with Therapy | Condition Interferes with Follow-up

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0348080
    UMLS CUI [1,2]
    C0521102
    UMLS CUI [1,3]
    C0021430
    UMLS CUI [2,1]
    C0348080
    UMLS CUI [2,2]
    C0521102
    UMLS CUI [2,3]
    C0087111
    UMLS CUI [3,1]
    C0348080
    UMLS CUI [3,2]
    C0521102
    UMLS CUI [3,3]
    C3274571
    Ritorna all'inizio della pagina

    Similar models

    Eligibility Hperglycemia NCT01585454

    1 moduli
    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    Age
    Item
    1. at least 18 years of age.
    boolean
    C0001779 (UMLS CUI [1])
    Receive Prenatal care
    Item
    2. receive prenatal care at the nurse midwifery/obstetrics service of pimc and plan to continue receiving such care throughout the pregnancy.
    boolean
    C1514756 (UMLS CUI [1,1])
    C0033052 (UMLS CUI [1,2])
    Oral Glucose Tolerance Test prior to Gestation weeks | Blood specimen Fasting | Plasma fasting glucose measurement | Hemoglobin A1c measurement | Glycated albumin measurement
    Item
    3. are able to have an ogtt prior to 16 weeks gestation (if diabetes was not previously diagnosed). hyperemesis can preclude some pregnant women from successfully completing the ogtt; these women will not be excluded if the fasting blood samples can be obtained. pregnant women with previously diagnosed diabetes are eligible if measures of glycemia (fpg, hba1c, glycated albumin) are completed prior to 16 weeks gestation.
    boolean
    C0029161 (UMLS CUI [1,1])
    C0332152 (UMLS CUI [1,2])
    C1135241 (UMLS CUI [1,3])
    C0178913 (UMLS CUI [2,1])
    C0015663 (UMLS CUI [2,2])
    C0583513 (UMLS CUI [3])
    C0474680 (UMLS CUI [4])
    C0523674 (UMLS CUI [5])
    Body mass index Prenatal Estimated
    Item
    4. estimated prenatal bmi > 25 kg/m2.
    boolean
    C1305855 (UMLS CUI [1,1])
    C2828394 (UMLS CUI [1,2])
    C0750572 (UMLS CUI [1,3])
    Protocol Compliance
    Item
    5. able to commit the time required for the interventions and follow-up.
    boolean
    C0525058 (UMLS CUI [1])
    Informed Consent
    Item
    6. able and willing to provide informed consent.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Medical contraindication Aerobic Exercise | Medical contraindication Resistance Training
    Item
    1. contraindication to aerobic or resistance exercise (acog, 2002).
    boolean
    C1301624 (UMLS CUI [1,1])
    C0001701 (UMLS CUI [1,2])
    C1301624 (UMLS CUI [2,1])
    C0872279 (UMLS CUI [2,2])
    Twin gestation | Multiple Pregnancy
    Item
    2. twin or multiple gestation.
    boolean
    C0744386 (UMLS CUI [1])
    C0032989 (UMLS CUI [2])
    Anemia, severe | Asthma Uncontrolled | Uncontrolled hypertension | Heart Disease | Condition Requirement Specialty care unit | Pregnancy At risk Maternal Death | Pregnancy At risk Fetal Death
    Item
    3. severe anemia, uncontrolled asthma, uncontrolled hypertension, cardiac disease, or any condition that requires follow-up at specialty care clinics outside of pimc (e.g., pregnancies at high risk for maternal or fetal demise).
    boolean
    C0238644 (UMLS CUI [1])
    C0004096 (UMLS CUI [2,1])
    C0205318 (UMLS CUI [2,2])
    C1868885 (UMLS CUI [3])
    C0018799 (UMLS CUI [4])
    C0348080 (UMLS CUI [5,1])
    C1514873 (UMLS CUI [5,2])
    C4034258 (UMLS CUI [5,3])
    C0032961 (UMLS CUI [6,1])
    C1444641 (UMLS CUI [6,2])
    C3494405 (UMLS CUI [6,3])
    C0032961 (UMLS CUI [7,1])
    C1444641 (UMLS CUI [7,2])
    C0015927 (UMLS CUI [7,3])
    Condition Interferes with Informed Consent | Condition Interferes with Therapy | Condition Interferes with Follow-up
    Item
    4. any condition that in the opinion of the investigators would interfere with consent, treatment, or follow-up.
    boolean
    C0348080 (UMLS CUI [1,1])
    C0521102 (UMLS CUI [1,2])
    C0021430 (UMLS CUI [1,3])
    C0348080 (UMLS CUI [2,1])
    C0521102 (UMLS CUI [2,2])
    C0087111 (UMLS CUI [2,3])
    C0348080 (UMLS CUI [3,1])
    C0521102 (UMLS CUI [3,2])
    C3274571 (UMLS CUI [3,3])
    Ritorna all'inizio della pagina 

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