ID

33889

Descripción

Mindfulness-based Behavioural Therapy (MIBT) Versus Psychodynamic Therapy for Patients With Major Depressive Disorder in Psychotherapeutic Day Treatment. A Randomised Clinical Pilot Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01070134

Link

https://clinicaltrials.gov/show/NCT01070134

Palabras clave

  1. 5/1/19 5/1/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

5 de enero de 2019

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Major Depressive Disorder NCT01070134

Eligibility Major Depressive Disorder NCT01070134

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. aged 18 to 65 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
2. major depressive disorder (scid i).
Descripción

Major Depressive Disorder

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1269683
3. bdi ii > 13.
Descripción

Beck Depression Inventory II score

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4273555
4. written informed consent.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. current psychosis, diagnosis of schizophrenia or schizotypal personality disorder (dsm iv-tr).
Descripción

Psychotic Disorders | Schizophrenia | Schizotypal Personality Disorder

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0033975
UMLS CUI [2]
C0036341
UMLS CUI [3]
C0036363
2. alcohol or substance abuse judged to require treatment in preference to depression (assessed during patient conference).
Descripción

Substance Use Disorders Treatment required for

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0038586
UMLS CUI [1,2]
C0332121
3. commenced or changed psychopharmacological treatment less than six weeks before randomisation.
Descripción

Psychopharmacological therapy Started | Psychopharmacological therapy Changed

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0679629
UMLS CUI [1,2]
C1272689
UMLS CUI [2,1]
C0679629
UMLS CUI [2,2]
C0392747
4. pregnancy.
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
5. no written informed consent.
Descripción

Informed Consent Lacking

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268

Similar models

Eligibility Major Depressive Disorder NCT01070134

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1. aged 18 to 65 years
boolean
C0001779 (UMLS CUI [1])
Major Depressive Disorder
Item
2. major depressive disorder (scid i).
boolean
C1269683 (UMLS CUI [1])
Beck Depression Inventory II score
Item
3. bdi ii > 13.
boolean
C4273555 (UMLS CUI [1])
Informed Consent
Item
4. written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Psychotic Disorders | Schizophrenia | Schizotypal Personality Disorder
Item
1. current psychosis, diagnosis of schizophrenia or schizotypal personality disorder (dsm iv-tr).
boolean
C0033975 (UMLS CUI [1])
C0036341 (UMLS CUI [2])
C0036363 (UMLS CUI [3])
Substance Use Disorders Treatment required for
Item
2. alcohol or substance abuse judged to require treatment in preference to depression (assessed during patient conference).
boolean
C0038586 (UMLS CUI [1,1])
C0332121 (UMLS CUI [1,2])
Psychopharmacological therapy Started | Psychopharmacological therapy Changed
Item
3. commenced or changed psychopharmacological treatment less than six weeks before randomisation.
boolean
C0679629 (UMLS CUI [1,1])
C1272689 (UMLS CUI [1,2])
C0679629 (UMLS CUI [2,1])
C0392747 (UMLS CUI [2,2])
Pregnancy
Item
4. pregnancy.
boolean
C0032961 (UMLS CUI [1])
Informed Consent Lacking
Item
5. no written informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial