ID

30938

Description

Management of Pain in Persons With Multiple Sclerosis; ODM derived from: https://clinicaltrials.gov/show/NCT00621374

Lien

https://clinicaltrials.gov/show/NCT00621374

Mots-clés

  1. 04/07/2018 04/07/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

4 juillet 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Multiple Sclerosis NCT00621374

Eligibility Multiple Sclerosis NCT00621374

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
chronic ongoing pain (i.e., pain at all times) with an average pain intensity of at least 4/10 on 0-10 numeric rating scale
Description

Chronic pain | Pain intensity Average Pain intensity rating scale

Type de données

boolean

Alias
UMLS CUI [1]
C0150055
UMLS CUI [2,1]
C1320357
UMLS CUI [2,2]
C1510992
UMLS CUI [2,3]
C1960637
pain is either worse or started since the onset of other ms symptoms.
Description

Pain Worse | Pain Associated with Multiple Sclerosis Symptoms

Type de données

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C1457868
UMLS CUI [2,1]
C0030193
UMLS CUI [2,2]
C0332281
UMLS CUI [2,3]
C0026769
UMLS CUI [2,4]
C1457887
pain of at least six months duration.
Description

Pain Duration

Type de données

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C0449238
reads, speaks and understands english.
Description

Able to read English Language | Able to speak English Language | Comprehension English Language

Type de données

boolean

Alias
UMLS CUI [1,1]
C0586740
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0564215
UMLS CUI [2,2]
C0376245
UMLS CUI [3,1]
C0233733
UMLS CUI [3,2]
C0376245
definitive diagnosis of multiple sclerosis (ms)
Description

Multiple Sclerosis

Type de données

boolean

Alias
UMLS CUI [1]
C0026769
at least 18 years of age
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
recruited from a recruitment source approved by the irb
Description

Patient Recruitment

Type de données

boolean

Alias
UMLS CUI [1]
C0242800
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe cognitive impairment resulting in the inability to verbally comprehend, learn, and recall new auditory verbal information, as reflected by a tics score of 20 or less.
Description

Severe cognitive impairment | Telephone Interview Cognitive status

Type de données

boolean

Alias
UMLS CUI [1]
C3554639
UMLS CUI [2,1]
C0021823
UMLS CUI [2,2]
C0945985
currently participating in counseling and/or psychotherapy more than once a week.
Description

Participation Counseling | Psychotherapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0010210
UMLS CUI [2]
C0033968
currently taking anti-psychotic medications
Description

Antipsychotic Agents

Type de données

boolean

Alias
UMLS CUI [1]
C0040615
has been hospitalized for psychiatric reasons in the past six months
Description

Hospitalization Due to Mental disorders

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0004936
experiencing current active suicidal ideation.
Description

Feeling suicidal

Type de données

boolean

Alias
UMLS CUI [1]
C0424000
has received treatment or participated in a clinical trial that involved significant elements of either cbt or hypnosis within the past year.
Description

Study Subject Participation Status | Therapy, Investigational | Cognitive Therapy | Hypnosis

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0949266
UMLS CUI [3]
C0009244
UMLS CUI [4]
C3888013

Similar models

Eligibility Multiple Sclerosis NCT00621374

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Chronic pain | Pain intensity Average Pain intensity rating scale
Item
chronic ongoing pain (i.e., pain at all times) with an average pain intensity of at least 4/10 on 0-10 numeric rating scale
boolean
C0150055 (UMLS CUI [1])
C1320357 (UMLS CUI [2,1])
C1510992 (UMLS CUI [2,2])
C1960637 (UMLS CUI [2,3])
Pain Worse | Pain Associated with Multiple Sclerosis Symptoms
Item
pain is either worse or started since the onset of other ms symptoms.
boolean
C0030193 (UMLS CUI [1,1])
C1457868 (UMLS CUI [1,2])
C0030193 (UMLS CUI [2,1])
C0332281 (UMLS CUI [2,2])
C0026769 (UMLS CUI [2,3])
C1457887 (UMLS CUI [2,4])
Pain Duration
Item
pain of at least six months duration.
boolean
C0030193 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Able to read English Language | Able to speak English Language | Comprehension English Language
Item
reads, speaks and understands english.
boolean
C0586740 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0564215 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0233733 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
Multiple Sclerosis
Item
definitive diagnosis of multiple sclerosis (ms)
boolean
C0026769 (UMLS CUI [1])
Age
Item
at least 18 years of age
boolean
C0001779 (UMLS CUI [1])
Patient Recruitment
Item
recruited from a recruitment source approved by the irb
boolean
C0242800 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Severe cognitive impairment | Telephone Interview Cognitive status
Item
severe cognitive impairment resulting in the inability to verbally comprehend, learn, and recall new auditory verbal information, as reflected by a tics score of 20 or less.
boolean
C3554639 (UMLS CUI [1])
C0021823 (UMLS CUI [2,1])
C0945985 (UMLS CUI [2,2])
Participation Counseling | Psychotherapy
Item
currently participating in counseling and/or psychotherapy more than once a week.
boolean
C0679823 (UMLS CUI [1,1])
C0010210 (UMLS CUI [1,2])
C0033968 (UMLS CUI [2])
Antipsychotic Agents
Item
currently taking anti-psychotic medications
boolean
C0040615 (UMLS CUI [1])
Hospitalization Due to Mental disorders
Item
has been hospitalized for psychiatric reasons in the past six months
boolean
C0019993 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0004936 (UMLS CUI [1,3])
Feeling suicidal
Item
experiencing current active suicidal ideation.
boolean
C0424000 (UMLS CUI [1])
Study Subject Participation Status | Therapy, Investigational | Cognitive Therapy | Hypnosis
Item
has received treatment or participated in a clinical trial that involved significant elements of either cbt or hypnosis within the past year.
boolean
C2348568 (UMLS CUI [1])
C0949266 (UMLS CUI [2])
C0009244 (UMLS CUI [3])
C3888013 (UMLS CUI [4])

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