ID

16067

Descrizione

Coordinating Center for Caregiver Intervention Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00177489

collegamento

https://clinicaltrials.gov/show/NCT00177489

Keywords

versioni (1)
  1. 27/06/16 27/06/16 -
Caricato su

27 giugno 2016

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Torna ai commenti del modello
Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Eligibility Dementia NCT00177489

Inglese

Eligibility Dementia NCT00177489

1 moduli  
  1. StudyEvent: Eligibility
    1. Eligibility Dementia NCT00177489
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
inclusion criteria:
Descrizione

inclusion criteria:

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1512693
1. age: 21 years or older
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
2. family member of the care recipient
Descrizione

family member of the care recipient

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0086282
3. must live with care recipient or share cooking facilities
Descrizione

family member housing with care recipient

Tipo di dati

boolean

4. must have a telephone that will enable use of ctis (computer telephone integration system) system
Descrizione

telephone capable of ctis use

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0039457
5. must plan to remain in the recruitment area for the duration of the intervention and follow-up
Descrizione

family member remaining in recruitment area

Tipo di dati

boolean

6. caregiver role for more than 6 months
Descrizione

caregiver role

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0086279
7. must provide on average 4 hours of supervision or direct assistance per day for the care recipient
Descrizione

average assistance time per day

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0516955
UMLS CUI [1,2]
C0449238
8. risk screening tool: must have a total score of at least 1 for questions 1-3, and a total of at least 2 for questions 4-9
Descrizione

risk screening score

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0449820
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. non-english, non-spanish speaking
Descrizione

english or spanish language skills

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0376245
UMLS CUI [1,2]
C0037750
2. active treatment (chemotherapy, radiation therapy) for cancer
Descrizione

cancer treatment

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0920425
3. imminent placement of care recipient into a nursing home or with another caregiver (within 6 months)
Descrizione

living in nursing home/assisted living facility

Tipo di dati

boolean

Alias
UMLS CUI [1]
C3841564
4. involvement in another clinical trial for caregivers
Descrizione

clinical trial participation status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
5. participant in reach i study
Descrizione

participant in reach

Tipo di dati

boolean

6. spmsq:> or = 4 errors*
Descrizione

Short Portable Mental Status Questionnaire

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0451291
if the caregiver has been inconsistent with answers or repeated answers during the screening process, then the interviewer administers the short portable mental status questionnaire (spmsq). if the caregiver missed 4 or more questions, he/she was excluded from the study.
Descrizione

exclusion through spmsq

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0451291
UMLS CUI [1,2]
C2828389
care recipient inclusion/exclusion criteria
Descrizione

care recipient inclusion/exclusion criteria

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C0680251
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
a. nincds (md diagnosis) of dementia or cognitive impairment (raw score on mmse of 23 or less)
Descrizione

nincds or mmse score

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2828081
UMLS CUI [2]
C1532985
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. non-english, non-spanish speaking
Descrizione

non-english, non-spanish speaking

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0376245
UMLS CUI [1,2]
C0037750
2. history of parkinson’s disease or a stroke with no reported decline in memory over the past year
Descrizione

history of parkinson or stroke

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0030567
UMLS CUI [2,1]
C0262926
UMLS CUI [2,2]
C0038454
3. active treatment (chemotherapy, radiation therapy) for cancer
Descrizione

active cancer treatment

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0920425
4. more than three acute medical hospitalizations in past year (other than psychiatric or alzheimer’s disease related admission)
Descrizione

non psychiatric or alzheimer related hospitalizations

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0019993
5. schizophrenia (onset of delusions before age 45) or other severe mental illness
Descrizione

schizophrenia or severe mental illness

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0036341
UMLS CUI [2]
C0004936
6. dementia secondary to head trauma (probable)
Descrizione

secondary dementia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0856416
7. blindness or deafness if either disability prohibits them from completion of data collection or participation in the interventions
Descrizione

blindness or deafness prohibiting clinical trial participation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0456909
UMLS CUI [2,1]
C0011053
UMLS CUI [2,2]
C1321605
UMLS CUI [2,3]
C0439801
UMLS CUI [2,4]
C0009488
8. mmse = 0 and bedbound (confined to a bed or chair for  22 hours per day, for at least 4 of the past 7 days)
Descrizione

mmse and bedbound

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1532985
UMLS CUI [1,2]
C0425251
9. planned nursing home admission in 6 months
Descrizione

planned nursing home admission

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1658399
10. participant in reach i study
Descrizione

participant in reach i study

Tipo di dati

boolean

Ritorna all'inizio della pagina

Similar models

Eligibility Dementia NCT00177489

1 moduli
  1. StudyEvent: Eligibility
    1. Eligibility Dementia NCT00177489
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
inclusion criteria:
Item
inclusion criteria:
boolean
C1512693 (UMLS CUI [1])
age
Item
1. age: 21 years or older
boolean
C0001779 (UMLS CUI [1])
family member of the care recipient
Item
2. family member of the care recipient
boolean
C0086282 (UMLS CUI [1])
family member housing with care recipient
Item
3. must live with care recipient or share cooking facilities
boolean
telephone capable of ctis use
Item
4. must have a telephone that will enable use of ctis (computer telephone integration system) system
boolean
C0039457 (UMLS CUI [1])
family member remaining in recruitment area
Item
5. must plan to remain in the recruitment area for the duration of the intervention and follow-up
boolean
caregiver role
Item
6. caregiver role for more than 6 months
boolean
C0086279 (UMLS CUI [1])
average assistance time per day
Item
7. must provide on average 4 hours of supervision or direct assistance per day for the care recipient
boolean
C0516955 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
risk screening score
Item
8. risk screening tool: must have a total score of at least 1 for questions 1-3, and a total of at least 2 for questions 4-9
boolean
C0449820 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
english or spanish language skills
Item
1. non-english, non-spanish speaking
boolean
C0376245 (UMLS CUI [1,1])
C0037750 (UMLS CUI [1,2])
cancer treatment
Item
2. active treatment (chemotherapy, radiation therapy) for cancer
boolean
C0920425 (UMLS CUI [1])
living in nursing home/assisted living facility
Item
3. imminent placement of care recipient into a nursing home or with another caregiver (within 6 months)
boolean
C3841564 (UMLS CUI [1])
clinical trial participation status
Item
4. involvement in another clinical trial for caregivers
boolean
C2348568 (UMLS CUI [1])
participant in reach
Item
5. participant in reach i study
boolean
Short Portable Mental Status Questionnaire
Item
6. spmsq:> or = 4 errors*
boolean
C0451291 (UMLS CUI [1])
exclusion through spmsq
Item
if the caregiver has been inconsistent with answers or repeated answers during the screening process, then the interviewer administers the short portable mental status questionnaire (spmsq). if the caregiver missed 4 or more questions, he/she was excluded from the study.
boolean
C0451291 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
care recipient inclusion/exclusion criteria
Item
care recipient inclusion/exclusion criteria
boolean
C0030705 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C0680251 (UMLS CUI [1,3])
Item Group
C1512693 (UMLS CUI)
nincds or mmse score
Item
a. nincds (md diagnosis) of dementia or cognitive impairment (raw score on mmse of 23 or less)
boolean
C2828081 (UMLS CUI [1])
C1532985 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
non-english, non-spanish speaking
Item
1. non-english, non-spanish speaking
boolean
C0376245 (UMLS CUI [1,1])
C0037750 (UMLS CUI [1,2])
history of parkinson or stroke
Item
2. history of parkinson’s disease or a stroke with no reported decline in memory over the past year
boolean
C0262926 (UMLS CUI [1,1])
C0030567 (UMLS CUI [1,2])
C0262926 (UMLS CUI [2,1])
C0038454 (UMLS CUI [2,2])
active cancer treatment
Item
3. active treatment (chemotherapy, radiation therapy) for cancer
boolean
C0920425 (UMLS CUI [1])
non psychiatric or alzheimer related hospitalizations
Item
4. more than three acute medical hospitalizations in past year (other than psychiatric or alzheimer’s disease related admission)
boolean
C0019993 (UMLS CUI [1])
schizophrenia or severe mental illness
Item
5. schizophrenia (onset of delusions before age 45) or other severe mental illness
boolean
C0036341 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
secondary dementia
Item
6. dementia secondary to head trauma (probable)
boolean
C0856416 (UMLS CUI [1])
blindness or deafness prohibiting clinical trial participation
Item
7. blindness or deafness if either disability prohibits them from completion of data collection or participation in the interventions
boolean
C0456909 (UMLS CUI [1])
C0011053 (UMLS CUI [2,1])
C1321605 (UMLS CUI [2,2])
C0439801 (UMLS CUI [2,3])
C0009488 (UMLS CUI [2,4])
mmse and bedbound
Item
8. mmse = 0 and bedbound (confined to a bed or chair for  22 hours per day, for at least 4 of the past 7 days)
boolean
C1532985 (UMLS CUI [1,1])
C0425251 (UMLS CUI [1,2])
planned nursing home admission
Item
9. planned nursing home admission in 6 months
boolean
C1658399 (UMLS CUI [1])
participant in reach i study
Item
10. participant in reach i study
boolean
Ritorna all'inizio della pagina 

Contatto

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Aiuto

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