ID

29973

Description

HARMONY Study (Hypertension Analysis of Stress Reduction Using Mindfulness Meditation and Yoga); ODM derived from: https://clinicaltrials.gov/show/NCT00825526

Lien

https://clinicaltrials.gov/show/NCT00825526

Mots-clés

Versions (2)
  1. 02/05/2018 02/05/2018 -
  2. 02/05/2018 02/05/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

2 mai 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Hypertension NCT00825526

Anglais

Eligibility Hypertension NCT00825526

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. age 20 to 75 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
2. hypertension by abpm at baseline (daytime > 135/85 mmhg or 24-hour abpm > 130/80 mmhg)
Description

Hypertensive disease | Ambulatory Blood Pressure Monitoring Daytime | 24-hour ambulatory blood pressure monitoring

Type de données

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2,1]
C0242876
UMLS CUI [2,2]
C0332169
UMLS CUI [3]
C2022220
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. use of antihypertensive within 6 months of the screening abpm.
Description

Antihypertensive Agents

Type de données

boolean

Alias
UMLS CUI [1]
C0003364
2. screening office bp > 180/100 and abpm > 160/100 mmhg.
Description

Blood pressure determination | Blood Pressure Monitoring, Ambulatory

Type de données

boolean

Alias
UMLS CUI [1]
C0005824
UMLS CUI [2]
C0242876
3. diabetes
Description

Diabetes Mellitus

Type de données

boolean

Alias
UMLS CUI [1]
C0011849
4. secondary hypertension
Description

Secondary hypertension

Type de données

boolean

Alias
UMLS CUI [1]
C0155616
5. renal disease (gfr < 60 ml/min or overt nephropathy)
Description

Kidney Diseases | Glomerular Filtration Rate | Other Coding

Type de données

boolean

Alias
UMLS CUI [1]
C0022658
UMLS CUI [2]
C0017654
UMLS CUI [3]
C3846158
6. history of heart attack
Description

Myocardial Infarction

Type de données

boolean

Alias
UMLS CUI [1]
C0027051
7. stroke or tia or
Description

Cerebrovascular accident | Transient Ischemic Attack

Type de données

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0007787
8. re-vascularization procedure.
Description

Revascularization

Type de données

boolean

Alias
UMLS CUI [1]
C0581603
9. active malignant disease (except non-melanoma skin cancer)
Description

Malignant Neoplasms | Exception Skin carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0699893
10. epileptic seizure 6 months before the screening visit.
Description

Epilepsy

Type de données

boolean

Alias
UMLS CUI [1]
C0014544
11. congestive heart failure
Description

Congestive heart failure

Type de données

boolean

Alias
UMLS CUI [1]
C0018802
12. severe liver disease
Description

Liver disease Severe

Type de données

boolean

Alias
UMLS CUI [1,1]
C0023895
UMLS CUI [1,2]
C0205082
13. pregnancy or lactation period
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
14. participation in a clinical trial or receipt of investigational compound or treatment in the 3 months prior to the initial screening visit.
Description

Study Subject Participation Status | Investigational New Drugs | Therapeutic procedure Recent

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C0332185
15. planned elective surgery during the study period except for cataract surgery
Description

Elective Surgical Procedures Planned | Exception Cataract surgery

Type de données

boolean

Alias
UMLS CUI [1,1]
C0206058
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C2939459
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Similar models

Eligibility Hypertension NCT00825526

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1. age 20 to 75 years
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease | Ambulatory Blood Pressure Monitoring Daytime | 24-hour ambulatory blood pressure monitoring
Item
2. hypertension by abpm at baseline (daytime > 135/85 mmhg or 24-hour abpm > 130/80 mmhg)
boolean
C0020538 (UMLS CUI [1])
C0242876 (UMLS CUI [2,1])
C0332169 (UMLS CUI [2,2])
C2022220 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Antihypertensive Agents
Item
1. use of antihypertensive within 6 months of the screening abpm.
boolean
C0003364 (UMLS CUI [1])
Blood pressure determination | Blood Pressure Monitoring, Ambulatory
Item
2. screening office bp > 180/100 and abpm > 160/100 mmhg.
boolean
C0005824 (UMLS CUI [1])
C0242876 (UMLS CUI [2])
Diabetes Mellitus
Item
3. diabetes
boolean
C0011849 (UMLS CUI [1])
Secondary hypertension
Item
4. secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Kidney Diseases | Glomerular Filtration Rate | Other Coding
Item
5. renal disease (gfr < 60 ml/min or overt nephropathy)
boolean
C0022658 (UMLS CUI [1])
C0017654 (UMLS CUI [2])
C3846158 (UMLS CUI [3])
Myocardial Infarction
Item
6. history of heart attack
boolean
C0027051 (UMLS CUI [1])
Cerebrovascular accident | Transient Ischemic Attack
Item
7. stroke or tia or
boolean
C0038454 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Revascularization
Item
8. re-vascularization procedure.
boolean
C0581603 (UMLS CUI [1])
Malignant Neoplasms | Exception Skin carcinoma
Item
9. active malignant disease (except non-melanoma skin cancer)
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
Epilepsy
Item
10. epileptic seizure 6 months before the screening visit.
boolean
C0014544 (UMLS CUI [1])
Congestive heart failure
Item
11. congestive heart failure
boolean
C0018802 (UMLS CUI [1])
Liver disease Severe
Item
12. severe liver disease
boolean
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
13. pregnancy or lactation period
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status | Investigational New Drugs | Therapeutic procedure Recent
Item
14. participation in a clinical trial or receipt of investigational compound or treatment in the 3 months prior to the initial screening visit.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C0087111 (UMLS CUI [3,1])
C0332185 (UMLS CUI [3,2])
Elective Surgical Procedures Planned | Exception Cataract surgery
Item
15. planned elective surgery during the study period except for cataract surgery
boolean
C0206058 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C2939459 (UMLS CUI [2,2])
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