Construct Validity and Reliability SCUES
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| ClinicalTrials.gov Identifier: NCT03600597 |
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Recruitment Status :
Completed
First Posted : July 26, 2018
Last Update Posted : July 27, 2018
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| Condition or disease |
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| Cerebral Palsy Upper Extremity Dysfunction |
| 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 |
- 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.
- 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 |
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
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
| Turkey | |
| Gazi University | |
| Ankara, Yeni̇mahalle, Turkey, 06560 | |
| Study Chair: | Bulent Elbasan | Study chair |
| 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 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Cerebral Palsy Brain Damage, Chronic Brain Diseases Central Nervous System Diseases Nervous System Diseases |

