ID

14100

Description

Exercise Training Versus Drug Therapy for Treating Depression in Older Adults; ODM derived from: https://clinicaltrials.gov/show/NCT00331305

Lien

https://clinicaltrials.gov/show/NCT00331305

Mots-clés

Versions (1)
  1. 29/03/2016 29/03/2016 -
Téléchargé le

29 mars 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Depression NCT00331305

Anglais

Eligibility Depression NCT00331305

1 Formulaires  
  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT00331305
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
dsm-iv diagnosis of major depressive disorder (mdd)
Description

DSM-IV diagnosis of major depressive disorder

Type de données

boolean

Alias
UMLS CUI [1]
C3710317
score of greater than 11 on the beck depression inventory (bdi)
Description

Beck depression inventory

Type de données

boolean

Alias
UMLS CUI [1]
C0451022
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
primary psychiatric diagnosis other than major depressive disorder (e.g., bipolar disorder)
Description

Psychiatric disorder except for major depressive disorder

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0332300
UMLS CUI [1,3]
C1269683
any of the following dsm-iv diagnoses: dementia or delirium; obsessive compulsive disorder (ocd); schizophrenia, schizoaffective, or other psychotic disorder; psychotic features, including any delusions or hallucinations during the current depressive episode; current alcohol or other substance abuse disorder; acute risk for suicide (e.g., score of greater than 2 on the suicide item on the ham-d) or acute risk for homicide
Description

Mental status

Type de données

boolean

Alias
UMLS CUI [1]
C0497327
UMLS CUI [2]
C0011206
UMLS CUI [3]
C0028768
UMLS CUI [4]
C0036341
UMLS CUI [5]
C0033975
UMLS CUI [6]
C0011253
UMLS CUI [7]
C0018524
UMLS CUI [8]
C0038586
UMLS CUI [9]
C1271074
UMLS CUI [10]
C0019872
may require treatment with additional psychotherapeutic agents (other than chloral hydrate for sleep) during the course of the study
Description

Psychotherapeutic agents except chloral hydrate

Type de données

boolean

Alias
UMLS CUI [1,1]
C0033978
UMLS CUI [1,2]
C0332300
UMLS CUI [1,3]
C0008161
significant medical conditions that may cause an increased risk for a significant adverse experience during the course of the trial (e.g., unstable angina, myocardial infarction within 3 months of study entry, etc.)
Description

Comorbidity

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
unable to be randomly assigned to the study drug due to a risk for adverse cardiac events, such as prolonged qt interval, use of other medications that would be counterindicated for use with sertraline, or other conditions that may make study participation unsafe
Description

Risk factors for study participation

Type de données

boolean

Alias
UMLS CUI [1]
C1556247
UMLS CUI [2,1]
C0074393
UMLS CUI [2,2]
C0687133
UMLS CUI [3]
C2348568
unable to be randomly assigned to an exercise condition due to medical conditions such as musculoskeletal problems or abnormal cardiac response to exercise (e.g., exercise-induced ventricular tachycardia, abnormal blood pressure response, etc.)
Description

Participation status limited by comorbidity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C2348568
currently receiving antidepressant medication or actively engaged in psychotherapy
Description

Antidepressant medication or psychotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C0003289
UMLS CUI [2]
C0033968
currently exercising regularly
Description

Exercising regularly

Type de données

boolean

Alias
UMLS CUI [1]
C0556454
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Similar models

Eligibility Depression NCT00331305

1 Formulaires
  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT00331305
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
DSM-IV diagnosis of major depressive disorder
Item
dsm-iv diagnosis of major depressive disorder (mdd)
boolean
C3710317 (UMLS CUI [1])
Beck depression inventory
Item
score of greater than 11 on the beck depression inventory (bdi)
boolean
C0451022 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Psychiatric disorder except for major depressive disorder
Item
primary psychiatric diagnosis other than major depressive disorder (e.g., bipolar disorder)
boolean
C0004936 (UMLS CUI [1,1])
C0332300 (UMLS CUI [1,2])
C1269683 (UMLS CUI [1,3])
Mental status
Item
any of the following dsm-iv diagnoses: dementia or delirium; obsessive compulsive disorder (ocd); schizophrenia, schizoaffective, or other psychotic disorder; psychotic features, including any delusions or hallucinations during the current depressive episode; current alcohol or other substance abuse disorder; acute risk for suicide (e.g., score of greater than 2 on the suicide item on the ham-d) or acute risk for homicide
boolean
C0497327 (UMLS CUI [1])
C0011206 (UMLS CUI [2])
C0028768 (UMLS CUI [3])
C0036341 (UMLS CUI [4])
C0033975 (UMLS CUI [5])
C0011253 (UMLS CUI [6])
C0018524 (UMLS CUI [7])
C0038586 (UMLS CUI [8])
C1271074 (UMLS CUI [9])
C0019872 (UMLS CUI [10])
Psychotherapeutic agents except chloral hydrate
Item
may require treatment with additional psychotherapeutic agents (other than chloral hydrate for sleep) during the course of the study
boolean
C0033978 (UMLS CUI [1,1])
C0332300 (UMLS CUI [1,2])
C0008161 (UMLS CUI [1,3])
Comorbidity
Item
significant medical conditions that may cause an increased risk for a significant adverse experience during the course of the trial (e.g., unstable angina, myocardial infarction within 3 months of study entry, etc.)
boolean
C0009488 (UMLS CUI [1])
Risk factors for study participation
Item
unable to be randomly assigned to the study drug due to a risk for adverse cardiac events, such as prolonged qt interval, use of other medications that would be counterindicated for use with sertraline, or other conditions that may make study participation unsafe
boolean
C1556247 (UMLS CUI [1])
C0074393 (UMLS CUI [2,1])
C0687133 (UMLS CUI [2,2])
C2348568 (UMLS CUI [3])
Participation status limited by comorbidity
Item
unable to be randomly assigned to an exercise condition due to medical conditions such as musculoskeletal problems or abnormal cardiac response to exercise (e.g., exercise-induced ventricular tachycardia, abnormal blood pressure response, etc.)
boolean
C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
Antidepressant medication or psychotherapy
Item
currently receiving antidepressant medication or actively engaged in psychotherapy
boolean
C0003289 (UMLS CUI [1])
C0033968 (UMLS CUI [2])
Exercising regularly
Item
currently exercising regularly
boolean
C0556454 (UMLS CUI [1])
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