ID

19281

Description

Reducing the Weight of Overweight Schizophrenia Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00158366

Link

https://clinicaltrials.gov/show/NCT00158366

Keywords

Versions (1)
  1. 12/18/16 12/18/16 -
Uploaded on

December 18, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Schizophrenia NCT00158366

English

Eligibility Schizophrenia NCT00158366

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of schizophrenia or schizoaffective disorder
Description

Schizophrenia | Schizoaffective Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0036341
UMLS CUI [2]
C0036337
body mass index (bmi) greater than 27
Description

Body mass index

Data type

boolean

Alias
UMLS CUI [1]
C1305855
stable on antipsychotic drug regimen for at least 1 month prior to study entry
Description

Antipsychotic drug therapy Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C1319421
UMLS CUI [1,2]
C0205360
parent or guardian willing to provide informed consent, if applicable
Description

Informed Consent parent | Informed Consent Guardian

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0030551
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1274041
positive and negative syndrome scale score less than 90
Description

Positive and negative syndrome scale

Data type

boolean

Alias
UMLS CUI [1]
C0451383
willing to use acceptable methods of contraception during the study
Description

Contraceptive methods Willing

Data type

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C0600109
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
medical contraindication for participating in a weight reduction/exercise program
Description

Medical contraindication Participation Weight Reduction Programs | Medical contraindication Participation Exercise therapy for weight loss

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C3179079
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0679823
UMLS CUI [2,3]
C3837639
mental retardation
Description

Mental Retardation

Data type

boolean

Alias
UMLS CUI [1]
C0025362
current enrollment in another weight management program
Description

Study Subject Participation Status | Weight maintenance regimen

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0920298
current use of weight reduction medication
Description

taking medication to lose weight

Data type

boolean

Alias
UMLS CUI [1]
C2054159
unstable cardiovascular or thyroid disease
Description

Cardiovascular Disease Unstable | Thyroid Disease Unstable

Data type

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0443343
UMLS CUI [2,1]
C0040128
UMLS CUI [2,2]
C0443343
active or end-stage renal disease
Description

Kidney Diseases | Kidney Failure, Chronic

Data type

boolean

Alias
UMLS CUI [1]
C0022658
UMLS CUI [2]
C0022661
psychiatric hospitalization within 1 month prior to study entry
Description

psychiatric hospitalization

Data type

boolean

Alias
UMLS CUI [1]
C0748061
current use of more than one anti-psychotic medication
Description

Antipsychotic Agents Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C0040615
UMLS CUI [1,2]
C1265611
pregnancy or breastfeeding
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
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Similar models

Eligibility Schizophrenia NCT00158366

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Schizophrenia | Schizoaffective Disorder
Item
diagnosis of schizophrenia or schizoaffective disorder
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
Body mass index
Item
body mass index (bmi) greater than 27
boolean
C1305855 (UMLS CUI [1])
Antipsychotic drug therapy Stable
Item
stable on antipsychotic drug regimen for at least 1 month prior to study entry
boolean
C1319421 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Informed Consent parent | Informed Consent Guardian
Item
parent or guardian willing to provide informed consent, if applicable
boolean
C0021430 (UMLS CUI [1,1])
C0030551 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1274041 (UMLS CUI [2,2])
Positive and negative syndrome scale
Item
positive and negative syndrome scale score less than 90
boolean
C0451383 (UMLS CUI [1])
Contraceptive methods Willing
Item
willing to use acceptable methods of contraception during the study
boolean
C0700589 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Participation Weight Reduction Programs | Medical contraindication Participation Exercise therapy for weight loss
Item
medical contraindication for participating in a weight reduction/exercise program
boolean
C1301624 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C3179079 (UMLS CUI [1,3])
C1301624 (UMLS CUI [2,1])
C0679823 (UMLS CUI [2,2])
C3837639 (UMLS CUI [2,3])
Mental Retardation
Item
mental retardation
boolean
C0025362 (UMLS CUI [1])
Study Subject Participation Status | Weight maintenance regimen
Item
current enrollment in another weight management program
boolean
C2348568 (UMLS CUI [1])
C0920298 (UMLS CUI [2])
taking medication to lose weight
Item
current use of weight reduction medication
boolean
C2054159 (UMLS CUI [1])
Cardiovascular Disease Unstable | Thyroid Disease Unstable
Item
unstable cardiovascular or thyroid disease
boolean
C0007222 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0040128 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
Kidney Diseases | Kidney Failure, Chronic
Item
active or end-stage renal disease
boolean
C0022658 (UMLS CUI [1])
C0022661 (UMLS CUI [2])
psychiatric hospitalization
Item
psychiatric hospitalization within 1 month prior to study entry
boolean
C0748061 (UMLS CUI [1])
Antipsychotic Agents Quantity
Item
current use of more than one anti-psychotic medication
boolean
C0040615 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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