ID

25401

Description

The Effect of Transcutaneous Electrical Nerve Stimulation on Quadriceps Central Activation and Gait; ODM derived from: https://clinicaltrials.gov/show/NCT00976079

Link

https://clinicaltrials.gov/show/NCT00976079

Keywords

Versions (1)
  1. 9/3/17 9/3/17 -
Uploaded on

September 3, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Tibial Femoral Knee Osteoarthritis NCT00976079

English

Eligibility Tibial Femoral Knee Osteoarthritis NCT00976079

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who have been diagnosed with a kellgren and lawrence grade of 1- 4 for tibial femoral knee oa in at least one leg or have been diagnosed with oa by a physician using evidence confirmed from imaging studies, arthroscopy, or visualization during an past surgical procedures, or have medical reports confirming oa using imaging studies, arthroscopy, or visualization during an past surgical procedures.
Description

Knee Osteoarthritis Tibial Femoral Kellgren-Lawrence score | Involvement with Leg Quantity | Degenerative polyarthritis Imaging studies | Degenerative polyarthritis Arthroscopy | Degenerative polyarthritis Visualization | Operative Surgical Procedures

Data type

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C0040184
UMLS CUI [1,3]
C0015811
UMLS CUI [1,4]
C3177117
UMLS CUI [2,1]
C1314939
UMLS CUI [2,2]
C1140621
UMLS CUI [2,3]
C1265611
UMLS CUI [3,1]
C0029408
UMLS CUI [3,2]
C1881134
UMLS CUI [4,1]
C0029408
UMLS CUI [4,2]
C0003904
UMLS CUI [5,1]
C0029408
UMLS CUI [5,2]
C2827662
UMLS CUI [6]
C0543467
patients between the ages of 18 and 80 years of age.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients will have a car less than 90%.
Description

Activation of muscle contraction Volition Percentage

Data type

boolean

Alias
UMLS CUI [1,1]
C2249837
UMLS CUI [1,2]
C0042950
UMLS CUI [1,3]
C0439165
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who are pregnant.
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
patients who have sought medical attention for a trauma to the knee injury within the past 6 months.
Description

Knee Injury

Data type

boolean

Alias
UMLS CUI [1]
C0022744
patients who have had any orthopaedic lower extremity surgery in the past 6 months, or any surgery that would inhibition proper functioning of the study methodology.
Description

Surgical procedure on lower extremity

Data type

boolean

Alias
UMLS CUI [1]
C0187763
patients with a diagnosis of rheumatoid arthritis.
Description

Rheumatoid Arthritis

Data type

boolean

Alias
UMLS CUI [1]
C0003873
patients with a known hypersensitivity to electrical stimulation.
Description

Hypersensitivity Electrical stimulation

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013786
patients with any types of neuropathy.
Description

Neuropathy Type Any

Data type

boolean

Alias
UMLS CUI [1,1]
C0442874
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C1552551
patients with known muscular abnormalities.
Description

Abnormality of the musculature

Data type

boolean

Alias
UMLS CUI [1]
C4021745
patients with a history of a heart condition that precludes them from exercise.
Description

Heart condition Excludes Exercise

Data type

boolean

Alias
UMLS CUI [1,1]
C3842523
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0015259
the technique can not be performed on the leg that has had a total knee replacement, but if the other leg meets the inclusion criteria the subject can perform the study on the non- reconstructed leg.
Description

Technique Unsuccessful Leg Total Knee Replacement

Data type

boolean

Alias
UMLS CUI [1,1]
C0449851
UMLS CUI [1,2]
C1272705
UMLS CUI [1,3]
C1140621
UMLS CUI [1,4]
C0086511
patients diagnosed with malignancy over the stimulating electrode site (thigh and knee).
Description

Malignant Neoplasm Electrical stimulation Site Thigh | Malignant Neoplasm Electrical stimulation Site Knee

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0013786
UMLS CUI [1,3]
C1515974
UMLS CUI [1,4]
C0039866
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0013786
UMLS CUI [2,3]
C1515974
UMLS CUI [2,4]
C0022742
patients with serious infection near the stimulating electrode sites (thigh and knee)
Description

Communicable Disease Serious | Electrical stimulation Site Thigh | Electrical stimulation Site Knee

Data type

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205404
UMLS CUI [2,1]
C0013786
UMLS CUI [2,2]
C1515974
UMLS CUI [2,3]
C0039866
UMLS CUI [3,1]
C0013786
UMLS CUI [3,2]
C1515974
UMLS CUI [3,3]
C0022742
patients have not had a knee injection in the past 2 weeks.
Description

Injection of knee joint Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0187946
UMLS CUI [1,2]
C0332197
patients who are unable to walk a series of 30 meters without a walking assistance device.
Description

Lacking Able to walk Meter Quantity | Walking assistive device Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C2712089
UMLS CUI [1,3]
C0475209
UMLS CUI [1,4]
C1265611
UMLS CUI [2,1]
C3874140
UMLS CUI [2,2]
C0332197
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Similar models

Eligibility Tibial Femoral Knee Osteoarthritis NCT00976079

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Knee Osteoarthritis Tibial Femoral Kellgren-Lawrence score | Involvement with Leg Quantity | Degenerative polyarthritis Imaging studies | Degenerative polyarthritis Arthroscopy | Degenerative polyarthritis Visualization | Operative Surgical Procedures
Item
patients who have been diagnosed with a kellgren and lawrence grade of 1- 4 for tibial femoral knee oa in at least one leg or have been diagnosed with oa by a physician using evidence confirmed from imaging studies, arthroscopy, or visualization during an past surgical procedures, or have medical reports confirming oa using imaging studies, arthroscopy, or visualization during an past surgical procedures.
boolean
C0409959 (UMLS CUI [1,1])
C0040184 (UMLS CUI [1,2])
C0015811 (UMLS CUI [1,3])
C3177117 (UMLS CUI [1,4])
C1314939 (UMLS CUI [2,1])
C1140621 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0029408 (UMLS CUI [3,1])
C1881134 (UMLS CUI [3,2])
C0029408 (UMLS CUI [4,1])
C0003904 (UMLS CUI [4,2])
C0029408 (UMLS CUI [5,1])
C2827662 (UMLS CUI [5,2])
C0543467 (UMLS CUI [6])
Age
Item
patients between the ages of 18 and 80 years of age.
boolean
C0001779 (UMLS CUI [1])
Activation of muscle contraction Volition Percentage
Item
patients will have a car less than 90%.
boolean
C2249837 (UMLS CUI [1,1])
C0042950 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
patients who are pregnant.
boolean
C0032961 (UMLS CUI [1])
Knee Injury
Item
patients who have sought medical attention for a trauma to the knee injury within the past 6 months.
boolean
C0022744 (UMLS CUI [1])
Surgical procedure on lower extremity
Item
patients who have had any orthopaedic lower extremity surgery in the past 6 months, or any surgery that would inhibition proper functioning of the study methodology.
boolean
C0187763 (UMLS CUI [1])
Rheumatoid Arthritis
Item
patients with a diagnosis of rheumatoid arthritis.
boolean
C0003873 (UMLS CUI [1])
Hypersensitivity Electrical stimulation
Item
patients with a known hypersensitivity to electrical stimulation.
boolean
C0020517 (UMLS CUI [1,1])
C0013786 (UMLS CUI [1,2])
Neuropathy Type Any
Item
patients with any types of neuropathy.
boolean
C0442874 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C1552551 (UMLS CUI [1,3])
Abnormality of the musculature
Item
patients with known muscular abnormalities.
boolean
C4021745 (UMLS CUI [1])
Heart condition Excludes Exercise
Item
patients with a history of a heart condition that precludes them from exercise.
boolean
C3842523 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
Technique Unsuccessful Leg Total Knee Replacement
Item
the technique can not be performed on the leg that has had a total knee replacement, but if the other leg meets the inclusion criteria the subject can perform the study on the non- reconstructed leg.
boolean
C0449851 (UMLS CUI [1,1])
C1272705 (UMLS CUI [1,2])
C1140621 (UMLS CUI [1,3])
C0086511 (UMLS CUI [1,4])
Malignant Neoplasm Electrical stimulation Site Thigh | Malignant Neoplasm Electrical stimulation Site Knee
Item
patients diagnosed with malignancy over the stimulating electrode site (thigh and knee).
boolean
C0006826 (UMLS CUI [1,1])
C0013786 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
C0039866 (UMLS CUI [1,4])
C0006826 (UMLS CUI [2,1])
C0013786 (UMLS CUI [2,2])
C1515974 (UMLS CUI [2,3])
C0022742 (UMLS CUI [2,4])
Communicable Disease Serious | Electrical stimulation Site Thigh | Electrical stimulation Site Knee
Item
patients with serious infection near the stimulating electrode sites (thigh and knee)
boolean
C0009450 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0013786 (UMLS CUI [2,1])
C1515974 (UMLS CUI [2,2])
C0039866 (UMLS CUI [2,3])
C0013786 (UMLS CUI [3,1])
C1515974 (UMLS CUI [3,2])
C0022742 (UMLS CUI [3,3])
Injection of knee joint Absent
Item
patients have not had a knee injection in the past 2 weeks.
boolean
C0187946 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Lacking Able to walk Meter Quantity | Walking assistive device Absent
Item
patients who are unable to walk a series of 30 meters without a walking assistance device.
boolean
C0332268 (UMLS CUI [1,1])
C2712089 (UMLS CUI [1,2])
C0475209 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,4])
C3874140 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
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