- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05661071
Neuropsychological Profiles of Children With Duchenne Muscular Dystrophy and Its Effects on Motor Functions
December 18, 2022 updated by: Esra Aldırmaz, Hacettepe University
Determination of Neuropsychological Profiles of Children With Duchenne Muscular Dystrophy and Investigation of Its Effects on Motor Functions
This study was planned to determine neuropsychological profiles of children with Duchenne Muscular Dystrophy and investigation of its effects on motor functions & compare to typically developed peers.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
- Other: Modified Mini Mental Test:
- Other: The Controlled Oral Word Association Test
- Other: The Central Nervous System Vital Signs
- Other: Conners' Parent Rating Scale-48 (Parent Report)
- Other: Child Behavior Checklist 6-18 ages (Parent Report)
- Other: Strengths and Difficulties Questionnaire (Self-Reported)
- Other: Brooke Lower Extremity Functional Classification
- Other: Motor Function Measurement-32 Items
- Other: Four Square Step Test
- Other: Six Minutes Walk Test
- Other: Timed Performance Test
Detailed Description
In this thesis, it is aimed to determine the neuropsychological profiles of children with Duchenne Muscular Dystrophy (DMD) and to investigate its effects on motor functions.
The study will be carried out with children between the ages of 7 and 16 who have been diagnosed with DMD as a result of genetic testing and who applied to Hacettepe University, Faculty of Physical Therapy and Rehabilitation, Pediatric Neuromuscular Diseases Unit for physiotherapy and rehabilitation evaluation.
In addition, considering the primary purpose of the study, typically developed boys between the ages of 7 and 16 with similar physical characteristics will be included in the study and compared with children with DMD.
Typically developed boys included in the study will be evaluated only with neuropsychological tests.
Evaluating cognitive function from neuropsychological tests; Modified Mini Mental Test, The Controlled Oral Word Association Test,computer-based The Central Nervous System Vital Signs will be applied.
To evaluate neurodevelopmental status from neuropsychological tests; Conners' Parent Rating Scale, Child Behavior Checklist, Strengths and Difficulties Questionnaire (SDQ) will be applied.
To evaluate the motor functions of individuals with DMD; Brooke Lower Extremity Functional Classification, Motor Function Measurement, Four Square Step Test, Six Minutes Walk Test, Timed Performance Tests (10 meters Walk/Run Test, Gower's (from a supine to a standing position), Right/Left Leg Standing, Ascent/Descent of 4 Steps) will be used.
In the study, in which the effect of the mutation region of dystrophin protein isoforms causing DMD on the neuropsychological profile of children will be investigated by comparing them with typically developed boys and the effect of this on motor function will be examined, the statistical significance level will be considered as p<0.05
Study Type
Observational
Enrollment (Actual)
74
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ankara, Turkey, 06100
- Hacettepe University, Faculty of Physical Therapy and Rehabilitation, Pediatric Neuromuscular Diseases Unit for physiotherapy and rehabilitation
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
3 years to 12 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
Children with Duchenne Muscular Dystrophy
Description
Inclusion Criteria:
- Having been diagnosed with DMD by a pediatric neurologist,
- Being between the ages of 7-16,
- Not to have any diagnosed chronic disease,
- Not having lost yet the ability to write and draw as required by neuropsychological assessments,
- Cooperate with the physiotherapist and be able to comply with their instructions.
Exclusion Criteria:
- Inability to cooperate adequately with the physiotherapist who made the evaluations,
- Have had any injury and/or surgery to the lower/upper extremities in the last 6 months, which may prevent the performance of motor function tests.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Duchenne Muscular Dystrophy
Children with Duchenne Muscular Dystrophy (DMD) between the ages of 7 and 16 who have been diagnosed with DMD as a result of genetic testing
|
To assess the cognitive function of children
To assess the cognitive function of children
To assess the cognitive function of children
To assess attention-deficit/hyperactivity disorder
To assesses both child adaptive behaviors and problem behaviors.
It is a brief emotional and behavioural screening questionnaire for children and young people.
To determine the functional status of the lower extremity
To assessment of motor function and progression of weakness in neuromuscular disorders
A test of dynamic balance and coordination that clinically assesses the participant's ability to step over objects forward, sideways, and backwards.
It evaluates the walking function and physical capacity of children at the submaximal level.
10 meters Walk& Run Test, Gower's(from a supine to a standing position), Right& Left Leg Standing, Ascent/Descent of 4 Steps
|
|
Typically Developed Children
Typically Developed Children with similar physical characteristics between the ages of 7 and 16
|
To assess the cognitive function of children
To assess the cognitive function of children
To assess the cognitive function of children
To assess attention-deficit/hyperactivity disorder
To assesses both child adaptive behaviors and problem behaviors.
It is a brief emotional and behavioural screening questionnaire for children and young people.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Modified Mini Mental Test
Time Frame: only baseline
|
The Mini Mental Test developed for adults was adapted to the pediatric population by making minor modifications.
Test; It evaluates verbal responses including attention, orientation, memory and language skills, ability to obey verbal and written orders, write spontaneous sentences, and copy a complex drawing.
The highest score that can be obtained from this test is 35, the lowest score is 0.
|
only baseline
|
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The Controlled Oral Word Association Test
Time Frame: only baseline
|
This test requires the individual to name as many words as possible that begin with a given letter, i.e.
K, A and S. Sixty seconds are allotted for each letter.
Individuals cannot use proper names or numbers and cannot use words with different tenses or endings once the root word has been given
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only baseline
|
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The Central Nervous System Vital Signs
Time Frame: only baseline
|
Central Nervous System Vital Signs is a reimbursable assessment procedure that utilizes computerized neuropsychological tests to evaluate the neurocognitive status of patients and covers a range of mental processes from simple motor performance, attention, memory, to executive functions.
|
only baseline
|
|
Conners' Parent Rating Scale-48 (Parent Report)
Time Frame: only baseline
|
The Conners' Parent Rating Scale-48 contains 48 items wherein the frequency of each item is rated on a 4-point Likert scale ranging from not at all (0)-3 very much (3).
The test has adequate psychometric properties and is widely used for clinical and research purposes with the attention deficit/hyperactivity disorder population
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only baseline
|
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Child Behavior Checklist 6-18 ages (Parent Report)
Time Frame: only baseline
|
The Child Behavior Checklist/6-18 assesses both child adaptive behaviors and problem behaviors.
There are 112 items that assess problem behaviors and 20 items that assess adaptive behavior.
Response format for problem behaviors is from 0 ("not true") to 2 ("very true").
The problem behavior items load onto two broad-band scales (Internalizing and Externalizing) and eight narrow-band scales (Rule Breaking, Aggressive Behavior, Withdrawn-Depressed, Somatic Complaints, Anxious Depressed, Social Problems, Thought Problems, and Attention Problems).
The adaptive behavior items load onto three scales: Activities, Social Competence, and School Competence.
A Total Competence and Total Behavior Problems score are also provided.
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only baseline
|
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Strengths and Difficulties Questionnaire (Self-Reported)
Time Frame: only baseline
|
The Strengths and Difficulties Questionnaire is a brief emotional and behavioural screening questionnaire for children and young people.
The tool can capture the perspective of children.
The 25 items in the test comprise 5 scales of 5 items each.
The scales include: emotional symptoms subscale, conduct problems subscale, hyperactivity/inattention subscale, peer relationships problem subscale, prosocial behaviour subscale.
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only baseline
|
|
Brooke Lower Extremity Functional Classification
Time Frame: only baseline
|
It was developed using the classification method based on "Vignos et al." to determine the functional status of the lower extremity.
It consists of 10 different levels, ranging from Level 1 (walks independently and climbs stairs) to Level 10 (bound to bed).
|
only baseline
|
|
Motor Function Measurement-32 Items
Time Frame: only baseline
|
The Motor Function Measure is a scale designed for the assessment of motor function and progression of weakness in neuromuscular disorders.
It is applicable to both ambulant and non-ambulant patients with a wide range of severity.
The scale exists in two versions, one with 32 items for patients over 6 years of age (MFM-32), the other with 20 items for children aged from 2 to 6 years (MFM-20).
Concerning the development of the scale, factor analysis identified three functional dimensions: D1 = standing position and transfers (13 items; 8 items in the short version), D2 = axial and proximal motor function (12 items; 8 in the short version), and D3 = distal motor function (7 items; 4 in the short version).
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only baseline
|
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Four Square Step Test
Time Frame: only baseline
|
It is a valid and reliable test that has been used frequently in children in recent years to evaluate dynamic balance.
Sticks, each 90 cm long, are placed on the floor to form 4 squares and the squares are numbered from 1 to 4. For the test to be completed successfully, the child must quickly move from one square to the next without touching the sticks.
Performance is determined by measuring the test completion time in seconds.
Shorter completion time means better dynamic balance.
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only baseline
|
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Six Minutes Walk Test
Time Frame: only baseline
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The 6-minutes walk test, which is valid and reliable for DMD patients, will evaluate the walking function and physical capacity of children at the submaximal level.
The distance the child walks for 6 minutes in a 25 m corridor will be recorded in meters.
A physiotherapist will walk with the children during the test and track the time with a stopwatch.
The test is simple and considered an important outcome measure for children with DMD.
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only baseline
|
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10 meters Walk& Run Test
Time Frame: only baseline
|
A 10-meter distance was marked on an unobstructed, flat surface using tape.
To limit the impact of acceleration and deceleration on gait speed, start and finish lines were placed 30 centimeter before and after the 10-meter distance.
Participants were instructed to begin with toes on the start line and walk or run as fast as possible, without compromising safety, to the finish line.
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only baseline
|
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Gower's(from a supine to a standing position)
Time Frame: only baseline
|
Children lied down on a mat with straight position and asked them to stand up as fast as possible.
Time was started when he moved and stopped when he was upright position.
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only baseline
|
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Right& Left Leg Standing Test
Time Frame: only baseline
|
Children had to maintain a one-legged stance for as long as they could with their eyes open, and allowing them to freely-move their arms.
Children were verbally encouraged to maintain the one-legged standing position for as long as possible during test.
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only baseline
|
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Ascent/Descent of 4 Steps
Time Frame: only baseline
|
The children were asked to climb up the 4-step ladder with double-sided handrails as fast as possible.
The time was started when his feet lifted from the ground and when both feet touched the ground, the time was stopped and recorded in seconds.
After climbing the ladder, they were asked to descend as fast as possible, the time was started when the foot was lifted, and the time was stopped when both feet touched the ground and recorded in seconds.
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only baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Genetic test report
Time Frame: only baseline
|
The effect of the mutation region of dystrophin protein isoforms causing DMD on the neuropsychological profile of children will be investigated by comparing them with typically developed boys and the effect of this on motor function will be examined.
|
only baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: İpek Gürbüz, Assc. Prof., Hacettepe University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 11, 2022
Primary Completion (Anticipated)
March 1, 2023
Study Completion (Anticipated)
March 1, 2023
Study Registration Dates
First Submitted
December 4, 2022
First Submitted That Met QC Criteria
December 18, 2022
First Posted (Actual)
December 22, 2022
Study Record Updates
Last Update Posted (Actual)
December 22, 2022
Last Update Submitted That Met QC Criteria
December 18, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GO22/310
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
Clinical Trials on Duchenne Muscular Dystrophy
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Dyne TherapeuticsRecruitingMuscular Dystrophies | Muscular Dystrophy, Duchenne | Duchenne Muscular Dystrophy (DMD) | Muscular Dystrophy, Duchenne and Becker Types | Genetic Disease, X-Linked | Genetic Disease, Inborn | DMD | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Muscular Dystrophy (DMD) | Muscular Dystrophies... and other conditionsUnited States
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Cairo UniversityCompletedMuscular Dystrophy, Duchenne TypeEgypt
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Santhera PharmaceuticalsTerminatedDuchenne Muscular Dystrophy (DMD)United States, Spain, Netherlands, Sweden, Germany, France, Belgium, United Kingdom, Italy, Ireland, Switzerland, Austria, Bulgaria, Hungary, Israel
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Sarepta Therapeutics, Inc.CompletedDuchenne Muscular Dystrophy (DMD)United States
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