- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06673251
School Readiness in Children with Type 1 Diabetes
Investigation of the Effects of Motor Performance, Sensory Processing, Quality of Life and Participation on School Readiness in Children with Type 1 Diabetes
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Arife Akbulut Akbulut, Lecturer
- Phone Number: +90 544-485-7922
- Email: arifeakbulut42@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Having been diagnosed with Type 1 DM in the last 6 months (for type 1 diabetes group) Being 60-78 months old
Exclusion Criteria:
- - Having any neurodevelopmental disorder in addition to diabetes (EX: cerebral palsy, down syndrome, muscular dystrophies..)
- Starting 1st grade
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy children
|
It does not include any intervention.
Only evaluation will be made.
|
|
children with type 1 diabetes
|
It does not include any intervention.
Only evaluation will be made.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
school readiness
Time Frame: through study completion, an average of 1 year
|
Marmara primary school school readiness scale (60-78 months) The scale consists of 2 forms: A. Development Form; It consists of a total of 153 behavioral items belonging to mental and language (74 items), socio-emotional (40 items), physical (23 items), self-care (16 items) skills. Each item is graded as "always, often, sometimes, never" to be filled by the teacher or parents according to the frequency of the child's behavior. B. Application Form; Mathematics (number recognition, increase-decrease, sets -color, shape-, ordering: 47 questions), Science (induction, deduction, problem solving: 14 questions), Sound (words starting with the same sound, rhyming words: 8 questions) Line (3 questions) Maze (2 questions) It consists of 5 sub-dimensions prepared to be answered by the child one-on-one in order to determine their success in their studies. Each question is scored (31) with (1) points for the correct answer and (0) points for the wrong answer. |
through study completion, an average of 1 year
|
|
motor performance
Time Frame: through study completion, an average of 1 year
|
Bruininks-Oseretsky Motor Proficiency Test 2- (BOT 2) BOT 2 will be used to assess motor proficiency in children.
BOT 2 is a test developed to assess fine and gross motor proficiency in children aged 4-21.
The test duration can vary between 40 and 60 minutes for a child.
The test consists of 8 subtests and 53 items.
The maximum score that can be obtained from the test is 243.
These are; fine motor skills (7 items - e.g.; Connecting the Dots), fine motor skill integrations (8 items - e.g.; Copying a Square), manual dexterity (5 items - e.g.; Classifying Shape Cards), bilateral coordination (7 items - e.g.; Sketch Jump), balance (9 items - e.g.; Walking on a Line), running speed and agility (5 items - e.g.; Sideways Jump on the Balance Beam), hand-arm coordination (7 items - e.g.; Dropping and Catching a Ball with Both Hands), strength (5 items - e.g.; Sit-up).
A total motor composite score is also obtained from the total score of all items
|
through study completion, an average of 1 year
|
|
Quality of Life
Time Frame: through study completion, an average of 1 year
|
Pediatric Quality of Life Inventory (PedsQL)) PedsQL is a scale developed to measure the health-related quality of life of children and adolescents between the ages of 2-18.
The PedsQL, which was developed for the ages of two to seven, was adapted into Turkish by Üneri and colleagues , and for the ages of 8-18 by Çakın, Memik and colleagues .
PedsQL has only parent-report forms for children between the ages of 2-5, and both self-report and parent forms for children/adolescents between the ages of 5-18.
PedsQL consists of 23 items.
|
through study completion, an average of 1 year
|
|
Sensory Processing
Time Frame: through study completion, an average of 1 year
|
The SPM Home Form consists of 75 items.
The scale is evaluated with eight subscales: Social Participation, Vision, Hearing, Touch, Body Awareness, Balance and Movement, Planning and Ideas, and Total Sensory Systems in children aged 5-12.
Total Sensory Systems represents the sum of the scores obtained from the Vision, Hearing, Touch, Body Awareness, Balance and Movement subscales and the Taste and Smell items, which are not subscales on their own.
Each item is evaluated according to the frequency of the behavior with the expressions Never, Sometimes, Often, and Always.
The Never option is given 1 point, the option is given 2 points, the option is given 3 points, and the option is given 4 points.
Each item is related to a basic sensory integration sensitivity.
In other words, the items can be interpreted as indicators of sensory overreactivity, underreactivity, sensory stimuli hunger, and a perception problem.
|
through study completion, an average of 1 year
|
|
participation
Time Frame: through study completion, an average of 1 year
|
The Participation and Environment Measure for Children and Youth (PEM-CY) questionnaire will be used.
The PEM-CY is a parent-report questionnaire used to assess participation and environmental factors in home, school, and community settings among children and youth ages 5-17.
The PEMCY participation items for each setting represent a broad range of activities typically performed in that setting.
For each activity type, parents are asked (a) how often their child participates (never=0 to every day=7); (b) how involved their child is when participating (at least=1 to a lot=5); and (c) whether they would like a change in their child's participation (no or yes).
Parents are then asked questions that include the PEM-CY environmental items for each setting.
Information is collected about whether certain features of the environment help children participate in activities in that environment (no problem, usually helps, sometimes helps/sometimes makes it difficult, usually makes it difficult)
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
physical fitness
Time Frame: through study completion, an average of 1 year
|
The Munich Physical Fitness Test (MFUT) will be used to assess the physical fitness of children.
The test consists of six different parameters including ball bouncing, target holding, forward bending, vertical jump, hanging and step test.
After all parameters are completed, the score for each parameter is calculated from the standardization table appropriate for age and gender, and this total score is divided by six and recorded as the Munich score (20).
MFUT has been shown to be a reliable and useful test in assessing important parameters of physical fitness such as strength, power, endurance, flexibility, speed, balance and coordination in children.
|
through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AYBU-AKBULUT-002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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