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Construct Validity and Reliability SCUES

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ClinicalTrials.gov Identifier: NCT03600597
Recruitment Status : Completed
First Posted : July 26, 2018
Last Update Posted : July 27, 2018
Sponsor:
Information provided by (Responsible Party):
Ayse Simsek, Gazi University

Brief Summary:
The aim of the study was to determine construct validity, discriminant validity and intra- and interrater reliability of the Selective Control of the Upper Extremity Scale (SCUES).

Condition or disease
Cerebral Palsy Upper Extremity Dysfunction

Detailed Description:
This study included children diagnosed with unilateral cerebral palsy. Children's upper extremity-selective motor controls were evaluated by video recording. Manual Ability Classification System and Taylor Hand Function Test were used to determine upper extremity functions

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Study Type : Observational
Actual Enrollment : 33 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Construct Validity and Reliability of the Selective Control of the Upper Extremity Scale in Children With Cerebral Palsy
Actual Study Start Date : April 10, 2017
Actual Primary Completion Date : March 10, 2018
Actual Study Completion Date : May 10, 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Cerebral Palsy




Primary Outcome Measures :
  1. Selective Control of the Extremity Scale [ Time Frame: 10 minutes ]
    SCUES administration required patients to perform specific isolated movement patterns at the shoulder (abduction/adduction), elbow (flexion/extension), forearm (supination/pronation), wrist (flexion/extension), and fingers/ thumb (grasp/release). Presence of mirror movements, movement of additional joints and motion less than available ROM are graded for movement at each joint level. Motion at each of the five joint levels is graded on a four-point scale: no SMC, moderately diminished SMC, mildly diminished SMC, and normal SMC.


Secondary Outcome Measures :
  1. Jebsen Taylor Hand Function Test [ Time Frame: 20 minutes ]
    The JTT measures movement, speed and manual dexterity. The subtests to assess hand function included turning over cards, simulated feeding, picking up small common objects, stacking checkers, picking up large objects, and picking up large heavy objects. Each task completion time was limited to 2 minutes.



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Ages Eligible for Study:   3 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Sampling Method:   Non-Probability Sample
Study Population
Children with Unilateral Cerebral Play
Criteria

Inclusion Criteria:

  • Ages between 3-18 years
  • Diagnosed as Cerebral Palsy (Hemiplegia)

Exclusion Criteria:

  • Participants with an unstable situation regarding their tonus-regulating medications
  • Participants had a botulinum toxin injection within the last 6 months, or any surgical correction within the last year

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03600597


Locations
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Turkey
Gazi University
Ankara, Yeni̇mahalle, Turkey, 06560
Sponsors and Collaborators
Gazi University
Investigators
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Study Chair: Bulent Elbasan Study chair
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Responsible Party: Ayse Simsek, Research assistant, Gazi University
ClinicalTrials.gov Identifier: NCT03600597    
Other Study ID Numbers: 77082166-302.08.01-
First Posted: July 26, 2018    Key Record Dates
Last Update Posted: July 27, 2018
Last Verified: July 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Cerebral Palsy
Brain Damage, Chronic
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases