ID

35681

Description

A Multi-level Life-span Characterization of Adult-depression and Effects of Medication and Exercise; ODM derived from: https://clinicaltrials.gov/show/NCT02407704

Lien

https://clinicaltrials.gov/show/NCT02407704

Mots-clés

Versions (1)
  1. 15/03/2019 15/03/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

15 mars 2019

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Depression NCT02407704

Anglais

Eligibility Depression NCT02407704

1 Formulaires  
  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT02407704
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. ages 25-39 and 65-79 years old
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
2. major depressive disorder (mdd), single or recurrent, as diagnosed by the prime-md
Description

Major Depressive Disorder | Major depressive disorder, recurrent

Type de données

boolean

Alias
UMLS CUI [1]
C1269683
UMLS CUI [2]
C0154409
3. madrs ≥ 15
Description

Montgomery-Asberg Depression Rating Scale Questionnaire

Type de données

boolean

Alias
UMLS CUI [1]
C4054475
4. in-town and available to commute to oakland for a 12-week period
Description

Residence Nearby

Type de données

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C1706276
5. study nurse practitioner approval to participate in a 12-week moderate intense exercise intervention
Description

Participation Exercise intervention Moderate intensity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C1831738
UMLS CUI [1,3]
C4081855
6. eligible to undergo mri
Description

Patients Eligible Magnetic Resonance Imaging

Type de données

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1548635
UMLS CUI [1,3]
C0024485
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. inability to provide informed consent.
Description

Informed Consent Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
2. modified mini-mental score (3ms) less than 84 or dementia based upon dsm-iv criteria including poor performance on the clinical neuropsychological battery, iqcode, and all available clinical information.
Description

Modified Mini-Mental State Examination score | Dementia Poor performance status Neuropsychological testing battery | Dementia Poor performance status IQCODE questionnaire | Dementia Clinical information

Type de données

boolean

Alias
UMLS CUI [1]
C4304091
UMLS CUI [2,1]
C0497327
UMLS CUI [2,2]
C1831741
UMLS CUI [2,3]
C2121096
UMLS CUI [3,1]
C0497327
UMLS CUI [3,2]
C1831741
UMLS CUI [3,3]
C3836253
UMLS CUI [4,1]
C0497327
UMLS CUI [4,2]
C2708733
3. lifetime diagnosis of bipolar i or ii disorder, schizophrenia, schizoaffective disorder, schizophreniform disorder, delusional disorder, or current psychotic symptoms.
Description

Bipolar I disorder Lifetime | Bipolar II disorder Lifetime | Schizophrenia Lifetime | Schizoaffective Disorder Lifetime | Schizophreniform Disorders Lifetime | Delusional disorder Lifetime | Psychotic symptom

Type de données

boolean

Alias
UMLS CUI [1,1]
C0853193
UMLS CUI [1,2]
C4071830
UMLS CUI [2,1]
C0236788
UMLS CUI [2,2]
C4071830
UMLS CUI [3,1]
C0036341
UMLS CUI [3,2]
C4071830
UMLS CUI [4,1]
C0036337
UMLS CUI [4,2]
C4071830
UMLS CUI [5,1]
C0036358
UMLS CUI [5,2]
C4071830
UMLS CUI [6,1]
C0011251
UMLS CUI [6,2]
C4071830
UMLS CUI [7]
C0871189
4. abuse of or dependence on alcohol or other substances within the past three months
Description

Substance Use Disorders | Substance Dependence

Type de données

boolean

Alias
UMLS CUI [1]
C0038586
UMLS CUI [2]
C0038580
5. high risk for suicide (e.g., active si and/or current/recent intent or plan) and unable to be managed safely in the clinical trial (e.g., unwilling to be hospitalized). urgent psychiatric referral will be made in these cases.
Description

High suicide risk | Feeling suicidal | Suicidal intent | Planning suicide | Disease Management Receive Unable | Hospitalization Unwilling | Referral to psychiatric hospital Urgent

Type de données

boolean

Alias
UMLS CUI [1]
C1271074
UMLS CUI [2]
C0424000
UMLS CUI [3]
C0582496
UMLS CUI [4]
C0424001
UMLS CUI [5,1]
C0376636
UMLS CUI [5,2]
C1514756
UMLS CUI [5,3]
C1299582
UMLS CUI [6,1]
C0019993
UMLS CUI [6,2]
C0558080
UMLS CUI [7,1]
C0850341
UMLS CUI [7,2]
C0439609
6. contraindication to venlafaxine xr as determined by study physician including history of intolerance of venlafaxine xr in the study target dosage range (venlafaxine xr at up to 300 mg/day).
Description

Medical contraindication Venlafaxine XR | Intolerance to Venlafaxine XR U/day

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0078569
UMLS CUI [1,3]
C1707968
UMLS CUI [2,1]
C1744706
UMLS CUI [2,2]
C0078569
UMLS CUI [2,3]
C1707968
UMLS CUI [2,4]
C0456683
7. inability to communicate in english (i.e., interview cannot be conducted without an interpreter; subject largely unable to understand questions and cannot respond in english).
Description

Lacking Able to communicate English Language

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C2364293
UMLS CUI [1,3]
C0376245
8. non-correctable clinically significant sensory impairment (i.e., cannot hear well enough to cooperate with interview)
Description

Hypesthesia | Correction Unsuccessful

Type de données

boolean

Alias
UMLS CUI [1]
C0020580
UMLS CUI [2,1]
C1947976
UMLS CUI [2,2]
C1272705
9. unstable/uncontrolled medical illness, including delirium, hypertension, hyperlipidemia, or cerebrovascular or cardiovascular risk factors that are not under medical management.
Description

Illness Unstable | Illness Uncontrolled | Delirium | Hypertensive disease | Hyperlipidemia | Risk factors Cerebrovascular | Cardiovascular risk factor

Type de données

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0443343
UMLS CUI [2,1]
C0221423
UMLS CUI [2,2]
C0205318
UMLS CUI [3]
C0011206
UMLS CUI [4]
C0020538
UMLS CUI [5]
C0020473
UMLS CUI [6,1]
C0035648
UMLS CUI [6,2]
C1880018
UMLS CUI [7]
C0850624
10. subjects taking psychotropic medications that cannot be safely tapered or discontinued prior to study initiation
Description

Psychotropic Drugs

Type de données

boolean

Alias
UMLS CUI [1]
C0033978
11. if a patient failed a trial of venlafaxine (12 weeks of treatment with venlafaxine including at least 6 weeks on 300mg/day), he/she would not be eligible.
Description

Venlafaxine U/day failed

Type de données

boolean

Alias
UMLS CUI [1,1]
C0078569
UMLS CUI [1,2]
C0456683
UMLS CUI [1,3]
C0231175
12. other drugs that may affect the gaba system will be excluded (e.g., kava, valerian, theanine, and gaba supplements).
Description

Pharmaceutical Preparations Affecting GABA Receptors | Kava preparation | Valerian root extract | theanine | GABA Supplements

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0206518
UMLS CUI [2]
C0939882
UMLS CUI [3]
C0795674
UMLS CUI [4]
C0076380
UMLS CUI [5,1]
C0016904
UMLS CUI [5,2]
C0242295
13. the drug linezolid (zyvox) should be discontinued prior to study enrollment and should not be used during the study.
Description

Linezolid To be stopped | Zyvox To be stopped

Type de données

boolean

Alias
UMLS CUI [1,1]
C0663241
UMLS CUI [1,2]
C1272691
UMLS CUI [2,1]
C0876226
UMLS CUI [2,2]
C1272691
14. exclusion criteria for mr scans include: cardiac pacemaker, aneurysm clip, cochlear implant, pregnancy, iud, shrapnel, history of metal fragments in the eye, neurostimulators, weight >250 lbs., tinnitus, or claustrophobia.
Description

Exclusion Criteria MRI scan | Artificial cardiac pacemaker | Aneurysm clip | Cochlear Implants | Pregnancy | Intrauterine Devices | Shrapnel | Metal foreign body in eye region | Neurostimulator | Excessive body weight gain | Tinnitus | Claustrophobia

Type de données

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0024485
UMLS CUI [2]
C0030163
UMLS CUI [3]
C0179977
UMLS CUI [4]
C0009199
UMLS CUI [5]
C0032961
UMLS CUI [6]
C0021900
UMLS CUI [7]
C0522670
UMLS CUI [8]
C0562528
UMLS CUI [9]
C0582124
UMLS CUI [10]
C0000765
UMLS CUI [11]
C0040264
UMLS CUI [12]
C0008909
15. current medical condition or treatment for a medical condition that could affect balance, gait, or contraindicate participation in moderate intensity physical activity.
Description

Medical condition Affecting Equilibrium | Medical condition Affecting Gait | Treatment Affecting Equilibrium | Treatment Affecting Gait | Medical contraindication Physical activity Moderate intensity

Type de données

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0014653
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C0016928
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C0392760
UMLS CUI [3,3]
C0014653
UMLS CUI [4,1]
C0087111
UMLS CUI [4,2]
C0392760
UMLS CUI [4,3]
C0016928
UMLS CUI [5,1]
C1301624
UMLS CUI [5,2]
C0026606
UMLS CUI [5,3]
C4081855
16. observed gait condition or use of walking assisted device that would contraindicate use of treadmill for exercise testing and intervention.
Description

Gait Condition | Use of Walking assistive device | Medical contraindication Treadmill Exercise test

Type de données

boolean

Alias
UMLS CUI [1,1]
C0016928
UMLS CUI [1,2]
C0348080
UMLS CUI [2,1]
C1524063
UMLS CUI [2,2]
C3874140
UMLS CUI [3,1]
C1301624
UMLS CUI [3,2]
C0184069
UMLS CUI [3,3]
C0015260
17. current congestive heart failure, angina, uncontrolled arrhythmia, or other symptoms indicative of an increased acute risk for a cardiovascular event; within the previous 12 months having a myocardial infarction, coronary artery bypass grafting, or angioplasty; conditions requiring chronic anticoagulation (i.e. recent or recurrent dvt).
Description

Congestive heart failure | Angina Pectoris | Cardiac Arrhythmia Uncontrolled | Symptoms At risk Cardiovascular event | Myocardial Infarction | Coronary Artery Bypass Surgery | Angioplasty | Condition Requirement Chronic anticoagulation | Deep Vein Thrombosis

Type de données

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0002962
UMLS CUI [3,1]
C0003811
UMLS CUI [3,2]
C0205318
UMLS CUI [4,1]
C1457887
UMLS CUI [4,2]
C1444641
UMLS CUI [4,3]
C1320716
UMLS CUI [5]
C0027051
UMLS CUI [6]
C0010055
UMLS CUI [7]
C0162577
UMLS CUI [8,1]
C0348080
UMLS CUI [8,2]
C1514873
UMLS CUI [8,3]
C0694554
UMLS CUI [9]
C0149871
18. eating disorders that would contraindicate physical activity.
Description

Eating Disorders | Medical contraindication Physical activity

Type de données

boolean

Alias
UMLS CUI [1]
C0013473
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0026606
19. report exercise on more than three days per week for greater than 20 minutes per day over the past three months.
Description

Exercise Duration/Frequency

Type de données

boolean

Alias
UMLS CUI [1,1]
C0015259
UMLS CUI [1,2]
C3669316
20. report plans to relocate to a location not accessible to the study site or having employment, personal, or travel commitments that prohibit attendance to at least 80 percent of the scheduled intervention sessions and all of the scheduled assessments.
Description

Relocation of home Planned | Commitment Preventing Protocol Compliance

Type de données

boolean

Alias
UMLS CUI [1,1]
C2699029
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0870312
UMLS CUI [2,2]
C1292733
UMLS CUI [2,3]
C0525058
21. current type i or ii diabetes
Description

Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
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Similar models

Eligibility Depression NCT02407704

1 Formulaires
  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT02407704
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1. ages 25-39 and 65-79 years old
boolean
C0001779 (UMLS CUI [1])
Major Depressive Disorder | Major depressive disorder, recurrent
Item
2. major depressive disorder (mdd), single or recurrent, as diagnosed by the prime-md
boolean
C1269683 (UMLS CUI [1])
C0154409 (UMLS CUI [2])
Montgomery-Asberg Depression Rating Scale Questionnaire
Item
3. madrs ≥ 15
boolean
C4054475 (UMLS CUI [1])
Residence Nearby
Item
4. in-town and available to commute to oakland for a 12-week period
boolean
C0237096 (UMLS CUI [1,1])
C1706276 (UMLS CUI [1,2])
Participation Exercise intervention Moderate intensity
Item
5. study nurse practitioner approval to participate in a 12-week moderate intense exercise intervention
boolean
C0679823 (UMLS CUI [1,1])
C1831738 (UMLS CUI [1,2])
C4081855 (UMLS CUI [1,3])
Patients Eligible Magnetic Resonance Imaging
Item
6. eligible to undergo mri
boolean
C0030705 (UMLS CUI [1,1])
C1548635 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Informed Consent Unable
Item
1. inability to provide informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Modified Mini-Mental State Examination score | Dementia Poor performance status Neuropsychological testing battery | Dementia Poor performance status IQCODE questionnaire | Dementia Clinical information
Item
2. modified mini-mental score (3ms) less than 84 or dementia based upon dsm-iv criteria including poor performance on the clinical neuropsychological battery, iqcode, and all available clinical information.
boolean
C4304091 (UMLS CUI [1])
C0497327 (UMLS CUI [2,1])
C1831741 (UMLS CUI [2,2])
C2121096 (UMLS CUI [2,3])
C0497327 (UMLS CUI [3,1])
C1831741 (UMLS CUI [3,2])
C3836253 (UMLS CUI [3,3])
C0497327 (UMLS CUI [4,1])
C2708733 (UMLS CUI [4,2])
Bipolar I disorder Lifetime | Bipolar II disorder Lifetime | Schizophrenia Lifetime | Schizoaffective Disorder Lifetime | Schizophreniform Disorders Lifetime | Delusional disorder Lifetime | Psychotic symptom
Item
3. lifetime diagnosis of bipolar i or ii disorder, schizophrenia, schizoaffective disorder, schizophreniform disorder, delusional disorder, or current psychotic symptoms.
boolean
C0853193 (UMLS CUI [1,1])
C4071830 (UMLS CUI [1,2])
C0236788 (UMLS CUI [2,1])
C4071830 (UMLS CUI [2,2])
C0036341 (UMLS CUI [3,1])
C4071830 (UMLS CUI [3,2])
C0036337 (UMLS CUI [4,1])
C4071830 (UMLS CUI [4,2])
C0036358 (UMLS CUI [5,1])
C4071830 (UMLS CUI [5,2])
C0011251 (UMLS CUI [6,1])
C4071830 (UMLS CUI [6,2])
C0871189 (UMLS CUI [7])
Substance Use Disorders | Substance Dependence
Item
4. abuse of or dependence on alcohol or other substances within the past three months
boolean
C0038586 (UMLS CUI [1])
C0038580 (UMLS CUI [2])
High suicide risk | Feeling suicidal | Suicidal intent | Planning suicide | Disease Management Receive Unable | Hospitalization Unwilling | Referral to psychiatric hospital Urgent
Item
5. high risk for suicide (e.g., active si and/or current/recent intent or plan) and unable to be managed safely in the clinical trial (e.g., unwilling to be hospitalized). urgent psychiatric referral will be made in these cases.
boolean
C1271074 (UMLS CUI [1])
C0424000 (UMLS CUI [2])
C0582496 (UMLS CUI [3])
C0424001 (UMLS CUI [4])
C0376636 (UMLS CUI [5,1])
C1514756 (UMLS CUI [5,2])
C1299582 (UMLS CUI [5,3])
C0019993 (UMLS CUI [6,1])
C0558080 (UMLS CUI [6,2])
C0850341 (UMLS CUI [7,1])
C0439609 (UMLS CUI [7,2])
Medical contraindication Venlafaxine XR | Intolerance to Venlafaxine XR U/day
Item
6. contraindication to venlafaxine xr as determined by study physician including history of intolerance of venlafaxine xr in the study target dosage range (venlafaxine xr at up to 300 mg/day).
boolean
C1301624 (UMLS CUI [1,1])
C0078569 (UMLS CUI [1,2])
C1707968 (UMLS CUI [1,3])
C1744706 (UMLS CUI [2,1])
C0078569 (UMLS CUI [2,2])
C1707968 (UMLS CUI [2,3])
C0456683 (UMLS CUI [2,4])
Lacking Able to communicate English Language
Item
7. inability to communicate in english (i.e., interview cannot be conducted without an interpreter; subject largely unable to understand questions and cannot respond in english).
boolean
C0332268 (UMLS CUI [1,1])
C2364293 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
Hypesthesia | Correction Unsuccessful
Item
8. non-correctable clinically significant sensory impairment (i.e., cannot hear well enough to cooperate with interview)
boolean
C0020580 (UMLS CUI [1])
C1947976 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
Illness Unstable | Illness Uncontrolled | Delirium | Hypertensive disease | Hyperlipidemia | Risk factors Cerebrovascular | Cardiovascular risk factor
Item
9. unstable/uncontrolled medical illness, including delirium, hypertension, hyperlipidemia, or cerebrovascular or cardiovascular risk factors that are not under medical management.
boolean
C0221423 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0221423 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
C0011206 (UMLS CUI [3])
C0020538 (UMLS CUI [4])
C0020473 (UMLS CUI [5])
C0035648 (UMLS CUI [6,1])
C1880018 (UMLS CUI [6,2])
C0850624 (UMLS CUI [7])
Psychotropic Drugs
Item
10. subjects taking psychotropic medications that cannot be safely tapered or discontinued prior to study initiation
boolean
C0033978 (UMLS CUI [1])
Venlafaxine U/day failed
Item
11. if a patient failed a trial of venlafaxine (12 weeks of treatment with venlafaxine including at least 6 weeks on 300mg/day), he/she would not be eligible.
boolean
C0078569 (UMLS CUI [1,1])
C0456683 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
Pharmaceutical Preparations Affecting GABA Receptors | Kava preparation | Valerian root extract | theanine | GABA Supplements
Item
12. other drugs that may affect the gaba system will be excluded (e.g., kava, valerian, theanine, and gaba supplements).
boolean
C0013227 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0206518 (UMLS CUI [1,3])
C0939882 (UMLS CUI [2])
C0795674 (UMLS CUI [3])
C0076380 (UMLS CUI [4])
C0016904 (UMLS CUI [5,1])
C0242295 (UMLS CUI [5,2])
Linezolid To be stopped | Zyvox To be stopped
Item
13. the drug linezolid (zyvox) should be discontinued prior to study enrollment and should not be used during the study.
boolean
C0663241 (UMLS CUI [1,1])
C1272691 (UMLS CUI [1,2])
C0876226 (UMLS CUI [2,1])
C1272691 (UMLS CUI [2,2])
Exclusion Criteria MRI scan | Artificial cardiac pacemaker | Aneurysm clip | Cochlear Implants | Pregnancy | Intrauterine Devices | Shrapnel | Metal foreign body in eye region | Neurostimulator | Excessive body weight gain | Tinnitus | Claustrophobia
Item
14. exclusion criteria for mr scans include: cardiac pacemaker, aneurysm clip, cochlear implant, pregnancy, iud, shrapnel, history of metal fragments in the eye, neurostimulators, weight >250 lbs., tinnitus, or claustrophobia.
boolean
C0680251 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0030163 (UMLS CUI [2])
C0179977 (UMLS CUI [3])
C0009199 (UMLS CUI [4])
C0032961 (UMLS CUI [5])
C0021900 (UMLS CUI [6])
C0522670 (UMLS CUI [7])
C0562528 (UMLS CUI [8])
C0582124 (UMLS CUI [9])
C0000765 (UMLS CUI [10])
C0040264 (UMLS CUI [11])
C0008909 (UMLS CUI [12])
Medical condition Affecting Equilibrium | Medical condition Affecting Gait | Treatment Affecting Equilibrium | Treatment Affecting Gait | Medical contraindication Physical activity Moderate intensity
Item
15. current medical condition or treatment for a medical condition that could affect balance, gait, or contraindicate participation in moderate intensity physical activity.
boolean
C3843040 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0014653 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0016928 (UMLS CUI [2,3])
C0087111 (UMLS CUI [3,1])
C0392760 (UMLS CUI [3,2])
C0014653 (UMLS CUI [3,3])
C0087111 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C0016928 (UMLS CUI [4,3])
C1301624 (UMLS CUI [5,1])
C0026606 (UMLS CUI [5,2])
C4081855 (UMLS CUI [5,3])
Gait Condition | Use of Walking assistive device | Medical contraindication Treadmill Exercise test
Item
16. observed gait condition or use of walking assisted device that would contraindicate use of treadmill for exercise testing and intervention.
boolean
C0016928 (UMLS CUI [1,1])
C0348080 (UMLS CUI [1,2])
C1524063 (UMLS CUI [2,1])
C3874140 (UMLS CUI [2,2])
C1301624 (UMLS CUI [3,1])
C0184069 (UMLS CUI [3,2])
C0015260 (UMLS CUI [3,3])
Congestive heart failure | Angina Pectoris | Cardiac Arrhythmia Uncontrolled | Symptoms At risk Cardiovascular event | Myocardial Infarction | Coronary Artery Bypass Surgery | Angioplasty | Condition Requirement Chronic anticoagulation | Deep Vein Thrombosis
Item
17. current congestive heart failure, angina, uncontrolled arrhythmia, or other symptoms indicative of an increased acute risk for a cardiovascular event; within the previous 12 months having a myocardial infarction, coronary artery bypass grafting, or angioplasty; conditions requiring chronic anticoagulation (i.e. recent or recurrent dvt).
boolean
C0018802 (UMLS CUI [1])
C0002962 (UMLS CUI [2])
C0003811 (UMLS CUI [3,1])
C0205318 (UMLS CUI [3,2])
C1457887 (UMLS CUI [4,1])
C1444641 (UMLS CUI [4,2])
C1320716 (UMLS CUI [4,3])
C0027051 (UMLS CUI [5])
C0010055 (UMLS CUI [6])
C0162577 (UMLS CUI [7])
C0348080 (UMLS CUI [8,1])
C1514873 (UMLS CUI [8,2])
C0694554 (UMLS CUI [8,3])
C0149871 (UMLS CUI [9])
Eating Disorders | Medical contraindication Physical activity
Item
18. eating disorders that would contraindicate physical activity.
boolean
C0013473 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C0026606 (UMLS CUI [2,2])
Exercise Duration/Frequency
Item
19. report exercise on more than three days per week for greater than 20 minutes per day over the past three months.
boolean
C0015259 (UMLS CUI [1,1])
C3669316 (UMLS CUI [1,2])
Relocation of home Planned | Commitment Preventing Protocol Compliance
Item
20. report plans to relocate to a location not accessible to the study site or having employment, personal, or travel commitments that prohibit attendance to at least 80 percent of the scheduled intervention sessions and all of the scheduled assessments.
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0870312 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
21. current type i or ii diabetes
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
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