- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04376372
Forced Lefthandedness in Neonatal Brachial Plexus Palsy (NBPP) Children (NBPP)
Forced Lefthandedness in Neonatal Brachial Plexus Palsy (NBPP) Children : is There a Neurophysiological and Functional Difference With Natural Lefthanders
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
Oost Vlaanderen
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Ghent, Oost Vlaanderen, Belgium, 9000
- Physical Medicine and Rehabilitation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- typical developing
- lefthanded
- NBPP or healthy
- righthanded parents
- 6-23 years
Exclusion Criteria:
- history of other locomotor or neurological disorder than NBPP
- history of brain surgery
- history of psychiatric disorder
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
TD_lefthanders
Typical developing lefthanded children and adolescents Assessment : sensibility, strength,writing,manual dexterity,degree of lefthandedness, body representation, movement analysis, motor control, quality of life, participation
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Electromyography only for cases (F-Lefthanders), not for controls (TD-lefthanders)
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F_lefthanders
Forced left handed NBPP children Assessment : sensibility, strength,writing,manual dexterity,degree of lefthandedness, body representation, movement analysis, motor control, quality of life, participation
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Electromyography only for cases (F-Lefthanders), not for controls (TD-lefthanders)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Strength-1
Time Frame: Baseline
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Medical Research Council Scale (MRC-scale) : score 0-5 ; 0 : no muscle contraction (worse) to 5 : normal power (better)
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Baseline
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Strength-2
Time Frame: Baseline
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Grip Strength (E-link) : Percent of the norm : higher = better
|
Baseline
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Strength-3
Time Frame: Baseline
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Active Movement scale (AMS): score 0-7 ; 0: no contraction to 7 : full motion
|
Baseline
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Sensibility hand
Time Frame: Baseline
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Semmes-Weinstein monofilament ( normal- abnormal)
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Baseline
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Handedness
Time Frame: Baseline
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Edinburgh Handedness Inventory (EDI) : Lateralization index: -100 (pure lefthander) to +100 (pure righthander)
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Baseline
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Baseline measure : brain imaging
Time Frame: Baseline
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Magnetic resonance imaging (MRI)
|
Baseline
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Baseline measure : movement pattern
Time Frame: Baseline
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Kinematic movement analysis (kinematic angels, kinetic forces, movement patterns)
|
Baseline
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Body representation
Time Frame: Baseline
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actual, implicit hand representation by drawings : mm
|
Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
quality of life-1
Time Frame: Baseline
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the Pediatric Outcome Data Collecting Instrument - dutch version • The PODCI consists of 5 domains: Upper Extremity and Physical Function, Transfers and Basic Mobility, Sports and Physical Functioning, Pain/Comfort, and Happiness. The "Global Functioning Score" is a mean of all domains except Happiness. The PODCI divides the ages into 2 groups: ages 2 to 10 years, which is filled out by the parent/guardian only, and ages 11 to 18 years, which has a questionnaire to be filled out by both the parents/guardians and the child. A raw score is created both for each domain and for the Global score, and can be compared with a normative standard |
Baseline
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quality of life-2
Time Frame: Baseline
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KIDSCREEN-52- dutch version : questionnaire of 52 items to be answered by the child/adolescent assessing Health related Quality of Life.
• The KIDSCREEN items use 5-point Likert-type scale.
Rasch scores are computed for each dimension and transformed into T-values with a mean of 50 and a standard deviation of 10; higher scores indicate better HRQoL and well-being.KIDSCREEN-52 T scores refer to the mean values and standard deviations from a multinational European sample
|
Baseline
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Activity-1
Time Frame: Baseline
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The Children's Hand-use Experience Questionnaire (CHEQ) is an online questionnaire for children from 6 to 18 years with unilateral upper limb impairment.
It is designed to measure children's own experiences when using the affected hand in common daily life activities requiring use of both hands.For children below the age of 13 years, it is recommended that parents act as proxy.
CHEQ is a computer-adaptive online questionnaire consisting of 29 items; available free of charge via the website (www.cheq.se).
Three scales are used to measure the grasp efficacy when both hands are involved, time utilization when performing the activity compared with peers, and experience of feeling bothered while performing the activities independently.
CHEQ scales are rated on a four-point ordinal scale and raw scores can be transformed by Rasch analysis to logits and further into a 0-100 CHEQ-units;Higher scores indicate a better grasp, less time taken, and greater satisfaction.
|
Baseline
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Activity-2
Time Frame: Baseline
|
Assisting Hand assessments (AHA).
The AHA is used to score object-related hand actions observed during a semi-structured test situation (10-20min) that elicits the use of both hands and which is suitable for different age groups.A transformation table of raw scores to interval-level 'AHA units' is available.
(0-100).
The higher the score the more the hand is properly used as assisted hand
|
Baseline
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Activity-3
Time Frame: Baseline
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The Melbourne Assessment is based on 16 items comprising tasks that are representative of the most important components of unilateral upper limb function (reach, grasp, release, and manipulate).
Most items are further subdivided in two to four sub-items that represent an aspect of the required movement, such as range of movement, fluency, target accuracy, speed, and quality of movement.
The total score can range from 0 to 122 points and can be converted to a percentage.
The higher the score, the better the unilateral limb function
|
Baseline
|
Activity-4
Time Frame: Baseline
|
The Purdue Pegboard Test is designed to assess fine motor hand function.
This assessment involves a series of four subtests that consist of placing small pins into holes on a pegboard and assembling pins and washers.
The subsets for preferred, non-preferred, and both hands require the patient to place the pins in the holes as quickly as possible, with the score being the number of pins placed in 30 s. Aged normed data are available.
|
Baseline
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shoulder function cases
Time Frame: Baseline
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mallet scale of shoulder function : 8 items.
In the Mallet score, shoulder movements are graded on a scale from 1 (no motion) to 5 (normal motion equal to that in the unaffected side), resulting in a maximum total score of 40.
A Mallet subscore of 4 or better is considered to be good shoulder function
|
Baseline
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Function( for cases)
Time Frame: Baseline
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Brachial plexus outcome measure (BPOM) :The BPOM is a, disease-specific, functional upper extremity assessment for children with NBPP.
It has 2 subscales: Activity and Self-evaluation.
The BPOM Activity subscale has 11 items, and each item is scored between 1 and 5 on an ordinal scale.
A score of1 indicates that the task cannot be completed, and a score of 5 indicates that the task can be completed with normal movement pattern.
The Activity subscale contains 3 parts: (1) shoulder, (2) elbow and forearm, and (3) wrist, finger, and thumb.
The BPOM Self-evaluation subscale consists of 2 visual analog scales to evaluate the working of the arm and hand and 1 visual analog scale to evaluate the appearance of the arm and hand of the child.
Several categories and items are evaluated simultaneously, and each score is calculated separately to define the function
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Baseline
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cognition
Time Frame: baseline
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Wechsler intelligence Scale for children: a short form consisting of subtests : (picture completion (PC), Vocabulary (V), Block Design (BD) and Similarities (S))of the WISC-III to estimate participant's intelligence. The subtest scores of the short form were transformed into deviation IQs (DIQ), based on mean intercorrelations from the standardization sample (Wechsler, 1991). • Classification : volgens DIQ
|
baseline
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muscle and nerve function
Time Frame: baseline
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electromyography (EMG)
|
baseline
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writing
Time Frame: baseline
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Vlaamse schrijftest : norms per age
|
baseline
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ruth Van der Looven, MD, Physical Medicine and Rehabilitation
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- B670201525721
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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