ID

36782

Beschrijving

High-intensity Exercise and Fall Prevention Boot Camp for Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT02230267

Link

https://clinicaltrials.gov/show/NCT02230267

Trefwoorden

Versies (1)
  1. 07-06-19 07-06-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

7 juni 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Parkinson's Disease NCT02230267

Engels

Eligibility Parkinson's Disease NCT02230267

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
neurologist-diagnosed idiopathic pd based on the uk pd brain bank criteria
Beschrijving

Parkinson Disease

Datatype

boolean

Alias
UMLS CUI [1]
C0030567
aged 45-85
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
hoehn and yahr stages 1-3 (mild to moderate pd)
Beschrijving

Parkinson Disease Mild Hoehn and Yahr Stage | Parkinson Disease Moderate Hoehn and Yahr Stage

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030567
UMLS CUI [1,2]
C2945599
UMLS CUI [1,3]
C3639483
UMLS CUI [2,1]
C0030567
UMLS CUI [2,2]
C0205081
UMLS CUI [2,3]
C3639483
participants do not anticipate a change in medication or surgical procedures in the next 8 months of the trial (2 months for the trial and 6 for the follow-up)
Beschrijving

Change of medication Absent | Change Operative Surgical Procedures Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0580105
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0392747
UMLS CUI [2,2]
C0543467
UMLS CUI [2,3]
C0332197
clearance from primary care physician to participate in the trial
Beschrijving

Study Subject Participation Status Approved

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0205540
must be stable on pd medication and dbs for 3 months prior to trial
Beschrijving

Antiparkinson Agents Stable | Deep Brain Stimulation Stable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003405
UMLS CUI [1,2]
C0205360
UMLS CUI [2,1]
C0394162
UMLS CUI [2,2]
C0205360
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
poorly controlled or unstable cardiovascular disease that precludes participation in exercise
Beschrijving

Cardiovascular Disease Poorly controlled | Cardiovascular Disease Unstable | Exercise participation Excluded

Datatype

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C3853134
UMLS CUI [2,1]
C0007222
UMLS CUI [2,2]
C0443343
UMLS CUI [3,1]
C0015259
UMLS CUI [3,2]
C0679823
UMLS CUI [3,3]
C0332196
moderate-to-severe dementia using the montreal cognitive assessment (moca). we will exclude participants with a moca cut off score of <26/30. this cut off value has excellent sensitivity (90%) and specificity (75%).
Beschrijving

Moderate dementia Montreal cognitive assessment | Severe dementia Montreal cognitive assessment

Datatype

boolean

Alias
UMLS CUI [1,1]
C3494871
UMLS CUI [1,2]
C3496286
UMLS CUI [2,1]
C3494652
UMLS CUI [2,2]
C3496286
inability to stand or walk for more than 10 minutes
Beschrijving

Lacking Able to stand Duration | Lacking Able to walk Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0560884
UMLS CUI [1,3]
C0449238
UMLS CUI [2,1]
C0332268
UMLS CUI [2,2]
C2712089
UMLS CUI [2,3]
C0449238
other significant disorders that would limit endurance exercise participation (i.e., osteoarthritis, stroke, respiratory problems, traumatic brain injury, neuromuscular disease, pain)
Beschrijving

Disease Limiting Exercise | Osteoarthritis | Cerebrovascular accident | Respiratory problem | Traumatic Brain Injury | Neuromuscular Diseases | Pain

Datatype

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0015259
UMLS CUI [2]
C0029408
UMLS CUI [3]
C0038454
UMLS CUI [4]
C1659989
UMLS CUI [5]
C0876926
UMLS CUI [6]
C0027868
UMLS CUI [7]
C0030193
already participating in a regular, vigorous exercise program (3x/week or more of >60% estimated maximum heart rate)
Beschrijving

Regular exercise Frequency | Vigorous exercise intensity Maximum heart rate

Datatype

boolean

Alias
UMLS CUI [1,1]
C0582191
UMLS CUI [1,2]
C0439603
UMLS CUI [2,1]
C3841230
UMLS CUI [2,2]
C0744679
participants will be excluded from the trial if they are taking any medications that interfere with heart rate response to exercise
Beschrijving

Medication Interferes with Heart rate response Exercise

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C1997754
UMLS CUI [1,4]
C0015259
Terug naar het begin van de pagina

Similar models

Eligibility Parkinson's Disease NCT02230267

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Parkinson Disease
Item
neurologist-diagnosed idiopathic pd based on the uk pd brain bank criteria
boolean
C0030567 (UMLS CUI [1])
Age
Item
aged 45-85
boolean
C0001779 (UMLS CUI [1])
Parkinson Disease Mild Hoehn and Yahr Stage | Parkinson Disease Moderate Hoehn and Yahr Stage
Item
hoehn and yahr stages 1-3 (mild to moderate pd)
boolean
C0030567 (UMLS CUI [1,1])
C2945599 (UMLS CUI [1,2])
C3639483 (UMLS CUI [1,3])
C0030567 (UMLS CUI [2,1])
C0205081 (UMLS CUI [2,2])
C3639483 (UMLS CUI [2,3])
Change of medication Absent | Change Operative Surgical Procedures Absent
Item
participants do not anticipate a change in medication or surgical procedures in the next 8 months of the trial (2 months for the trial and 6 for the follow-up)
boolean
C0580105 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392747 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Study Subject Participation Status Approved
Item
clearance from primary care physician to participate in the trial
boolean
C2348568 (UMLS CUI [1,1])
C0205540 (UMLS CUI [1,2])
Antiparkinson Agents Stable | Deep Brain Stimulation Stable
Item
must be stable on pd medication and dbs for 3 months prior to trial
boolean
C0003405 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0394162 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Cardiovascular Disease Poorly controlled | Cardiovascular Disease Unstable | Exercise participation Excluded
Item
poorly controlled or unstable cardiovascular disease that precludes participation in exercise
boolean
C0007222 (UMLS CUI [1,1])
C3853134 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
C0015259 (UMLS CUI [3,1])
C0679823 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])
Moderate dementia Montreal cognitive assessment | Severe dementia Montreal cognitive assessment
Item
moderate-to-severe dementia using the montreal cognitive assessment (moca). we will exclude participants with a moca cut off score of <26/30. this cut off value has excellent sensitivity (90%) and specificity (75%).
boolean
C3494871 (UMLS CUI [1,1])
C3496286 (UMLS CUI [1,2])
C3494652 (UMLS CUI [2,1])
C3496286 (UMLS CUI [2,2])
Lacking Able to stand Duration | Lacking Able to walk Duration
Item
inability to stand or walk for more than 10 minutes
boolean
C0332268 (UMLS CUI [1,1])
C0560884 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C2712089 (UMLS CUI [2,2])
C0449238 (UMLS CUI [2,3])
Disease Limiting Exercise | Osteoarthritis | Cerebrovascular accident | Respiratory problem | Traumatic Brain Injury | Neuromuscular Diseases | Pain
Item
other significant disorders that would limit endurance exercise participation (i.e., osteoarthritis, stroke, respiratory problems, traumatic brain injury, neuromuscular disease, pain)
boolean
C0012634 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
C0029408 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C1659989 (UMLS CUI [4])
C0876926 (UMLS CUI [5])
C0027868 (UMLS CUI [6])
C0030193 (UMLS CUI [7])
Regular exercise Frequency | Vigorous exercise intensity Maximum heart rate
Item
already participating in a regular, vigorous exercise program (3x/week or more of >60% estimated maximum heart rate)
boolean
C0582191 (UMLS CUI [1,1])
C0439603 (UMLS CUI [1,2])
C3841230 (UMLS CUI [2,1])
C0744679 (UMLS CUI [2,2])
Medication Interferes with Heart rate response Exercise
Item
participants will be excluded from the trial if they are taking any medications that interfere with heart rate response to exercise
boolean
C0013227 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C1997754 (UMLS CUI [1,3])
C0015259 (UMLS CUI [1,4])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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