ID

30938

Descrizione

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

collegamento

https://clinicaltrials.gov/show/NCT00621374

Keywords

versioni (1)
  1. 04/07/18 04/07/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

4 luglio 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT00621374

Inglese

Eligibility Multiple Sclerosis NCT00621374

1 moduli  
Inclusion Criteria
Descrizione

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
Descrizione

Chronic pain | Pain intensity Average Pain intensity rating scale

Tipo di dati

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.
Descrizione

Pain Worse | Pain Associated with Multiple Sclerosis Symptoms

Tipo di dati

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.
Descrizione

Pain Duration

Tipo di dati

boolean

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

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

Tipo di dati

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)
Descrizione

Multiple Sclerosis

Tipo di dati

boolean

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

Age

Tipo di dati

boolean

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

Patient Recruitment

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0242800
Exclusion Criteria
Descrizione

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.
Descrizione

Severe cognitive impairment | Telephone Interview Cognitive status

Tipo di dati

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.
Descrizione

Participation Counseling | Psychotherapy

Tipo di dati

boolean

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

Antipsychotic Agents

Tipo di dati

boolean

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

Hospitalization Due to Mental disorders

Tipo di dati

boolean

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

Feeling suicidal

Tipo di dati

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.
Descrizione

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

Tipo di dati

boolean

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

Eligibility Multiple Sclerosis NCT00621374

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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