Reliability and Validity of a Computerized Tool to Assess Proprioception Among Children With Coordination Disorders

Coordination disorders are common among children that arrive to child development services. Children with coordination disorders have impaired proprioceptive sensation and motor planning. It is important to carry out a comprehensive assessment of these children in order to design an appropriate and effective treatment. There is a lack of an objective and standard assessment tools for proprioception and motor planning. Technology based assessment tools might offer a solution, as they enable automated and accurate measurement. The purpose of this study is to examine the validity and reliability of a new diagnostic computerized kit, which was developed for assessment of proprioception and motor planning among children with coordination disorders. The hypothesis includes:

1. Examine the construct validity of the new diagnostic computerized kit (the known group procedure). Whether there is a difference in the outcomes between children with typical development and children with coordination disorders.
2. Examine the construct validity of the new diagnostic computerized kit outcomes - correlation with the following associated variables: (a) motor skills; (b) sensory function; (c) participation in daily activities.
3. Examine of test-retest reliability of the new diagnostic computerized kit. Whether the outcomes are stable in repeated measurements.

The participants will include fifty children between the ages of 5 to 7 years: 25 children with coordination disorders (study group), and 25 children with typical development (control group).

Each child will arrive for an evaluation meeting that includes: (a) the new diagnostic computerized kit; (b) standard and routine tests for motor skills (Movement Assessment Battery for Children-2-MABC-2, and two sub-test of the Beery-Buktenica developmental test of visual-motor integration- Beery VMI). In addition, the children's parents will complete two questionnaires: (a) Sensory Processing Measurement (SPM) for sensory function assessment; (b) Participation in Childhood Occupations Questionnaire (PICO-Q) for daily participation assessment. After two weeks, ten children from the control group will be evaluated once again by the new diagnostic computerized kit for examine test-retest reliability.

Study Overview

• Status: Completed
• Conditions: Developmental Coordination Disorder; Developmental Dyspraxia; Clumsy Child Syndrome

Detailed Description

Coordination disorders are common among children that arrive to child development services. Children with coordination disorders have impaired proprioceptive sensation and motor planning. It is important to carry out a comprehensive assessment of these children in order to design an appropriate and effective treatment. There is a lack of an objective and standard assessment tools for proprioception and motor planning. Technology based assessment tools might offer a solution, as they enable automated and accurate measurement. The purpose of this study is to examine the validity and reliability of a new diagnostic computerized kit, which was developed for assessment of proprioception and motor planning among children with coordination disorders.

The new diagnostic computerized kit consists a computerized thumb- fingers matching test (for proprioception).

The hypothesis includes:

1. Examine the construct validity of the new diagnostic computerized kit (the known group procedure). Whether there is a difference in the outcomes between children with typical development and children with coordination disorders.
2. Examine the construct validity of the new diagnostic computerized kit outcomes - correlation with the following associated variables: (a) motor skills; (b) sensory function; (c) participation in daily activities.
3. Examine of test-retest reliability of the new diagnostic computerized kit. Whether the outcomes are stable in repeated measurements.

The participants will include fifty children between the ages of 5 to 7 years: 25 children with coordination disorders (study group) in a waiting list for an occupational therapy evaluation (in Orlansky Children's Development Center, Dan -Petah Tikva Region, Clalit Health Services), and 25 children with typical development (control group).

The participants will be recruited by a convenience sample. Participation in the study will be offered by telephone to parents of children who may meet the inclusion /exclusion criteria. For the study group the recruitment will be to children in a waiting list for an occupational therapy evaluation (in Orlansky Children's Development Center). For the control group, the recruitment will be by a snowball sample (a friend brings a friend), through acquaintances of the investigators. Children whose parents agree to participate in the study will attend one meeting, accompanied by at least one parent. At the beginning of the meeting, the parents will receive a detailed explanation about the purpose and the study process. The new diagnostic computerized kit will be presented and explained how to use it. Parents will be assured total privacy. In addition, parents of children from the study group will be told that their child's medical record will be used to ensure inclusion and exclusion criteria. Parents who express their consent to participate in the study will sign an informed consent form and then complete a demographic questionnaire and a screening questionnaire. Children that will be find suitable for the study will Be evaluated by: (a) the new diagnostic computerized kit; (b) standard and routine tests for motor skills (Movement Assessment Battery for Children-2-MABC-2, and two sub-test of the Beery-Buktenica developmental test of visual-motor integration- Beery VMI). In addition, the children's parents will complete two questionnaires: (a) Sensory Processing Measurement (SPM) for sensory function assessment; (b) Participation in Childhood Occupations Questionnaire (PICO-Q) for daily participation assessment. After two weeks, ten children from the control group will be evaluated once again by the new diagnostic computerized kit for examine test-retest reliability.

Analysis of the data will be done using the SPSS version 32. Descriptive statistics will be used for description of the population and the variables. Shapiro-wilks test will be used to examine the type of distribution of the dependent variables. According to the type of distribution will use t-test for two independent samples or Mann-Whitney test to examine the differences between groups (hypothesis 1). Pearson Correlation Coefficient test or Spearman's Rank Correlation Coefficient test will be used to examine correlation between the outcomes of the assessment tools (hypothesis 2 and 3). The significance level for all the statistical tests will be p<0.05.

• Study Type: Observational
• Enrollment (Actual): 52

Contacts and Locations

Study Locations

• Israel
  • Petach Tikva, Israel
    • Orlansky,Clalit Health Services

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 3 years to 5 years (Child)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

The participants will include fifty children between the ages of 5 to 7 years:

the study group - 25 children in a waiting list for an occupational therapy evaluation (in Orlansky Children's Development Center, Dan -Petah Tikva Region, Clalit Health Services), the control group - 25 children with typical development.

Description

Inclusion Criteria:

• Children aged 5-7, insured by "Clalit Health Services", and their parents. Inclusion into groups will be done according to the DCDQ'07 Developmental Questionnaire (DCDQ'07).
• Inclusion to study group: children in a waiting list for an occupational therapy evaluation due to difficulties in fine or gross motor difficulties in performing daily activities as self-treatment, Play and recreation, and suspicion of developmental delay and DCD. children are able to communicate and understand instructions in Hebrew, and their parents know the Hebrew language at the level of reading and writing. A score of 15-46 indicating DCD or suspected DCD in the DCDQ'07 questionnaire.
• Inclusion into control group: healthy children with a typical development who are able to communicate and understand Hebrew instructions, and whose parents know the Hebrew language at the level of reading and writing. A score of 47-75 indicates that there is no DCD in the DCDQ'07 questionnaire.

Exclusion Criteria:

• Children with developmental syndromes such as autism, cerebral palsy, orthopedic or neurological diseases, including sensory systems, such as impaired vision, will not be included in the study (according to parents' questioning, if no information will be available in the medical record). Children who study in special education frames (according to parental questioning) will not be included in the study. Children who have previously been treated in occupational therapy will not included.

Study Plan

How is the study designed?

Design Details

• Observational Models: Case-Control
• Time Perspectives: Cross-Sectional

Number of groups / cohorts

2

Cohorts and Interventions

Group / Cohort
Study group; Children with coordination disorder between the ages of 5 to 7 years.
control group; children with typical development between the ages of 5 to 7 years.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Total time- outcome of the new diagnostic computerized kit - computerized thumb fingers matching test.	Time is one of the outcome measures of the computerized thumb fingers matching test, that is measured in a ratio scale.	Time duration for this test is 5 minutes.
Standard Deviation (SD) of touch time- outcome of the new diagnostic computerized kit - computerized thumb fingers matching test.	Standard Deviation (SD) of touch time is one of the outcome measures of the computerized thumb fingers matching test, that is measured in a ratio scale by sensors of the touches.	Time duration for this test is 5 minutes.
Correct sequence- outcome of the new diagnostic computerized kit - computerized thumb fingers matching test.	Correct sequence is one of the outcome measures of the computerized thumb fingers matching test, that is measured in a ratio scale by sensors of the touches.	Time duration for this test is 5 minutes.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Visual-motor integration outcome of the Beery-Buktenica developmental test of visual-motor integration (Beery VMI).	Visual-motor integration grade is measured in a ratio scale from the Beery VMI test.	Time duration for this test is 10 minutes. only one time point
Motor coordination outcome of the Beery-Buktenica developmental test of visual-motor integration (Beery VMI).	Motor coordination grade is measured in a ratio scale from the Beery VMI test.	Time duration for this test is 5 minutes. only one time point
Physical awareness outcome of the Sensory Processing Measurement (SPM).	Questionaire for the parents that is measured in a Likert scale.	Time duration for this questionaire is 20 minutes. only one time point
Balance and movement outcome of the Sensory Processing Measurement (SPM) .	Questionaire for the parents that is measured in a Likert scale.	Time duration for this questionaire is 20 minutes. only one time point
Planning and ideation outcome of the Sensory Processing Measurement (SPM).	Questionaire for the parents that is measured in a Likert scale.	Time duration for this questionaire is 20 minutes. only one time point
Total sensory systems outcome of the Sensory Processing Measurement (SPM).	Questionaire for the parents that is measured in a Likert scale.	Time duration for this questionaire is 20 minutes. only one time point
Difficulty in performance outcome of the Participation in Childhood Occupations Questionaire (PICO-Q).	Questionaire for the parents that is measured in a Likert scale.	Time duration for this questionaire is 15 minutes. only one time point
Frequency of performance outcome of the Participation in Childhood Occupations Questionaire (PICO-Q).	Questionaire for the parents that is measured in a Likert scale.	Time duration for this questionaire is 15 minutes. only one time point
Enjoyment outcome of the Participation in Childhood Occupations Questionaire (PICO-Q).	Questionaire for the parents that is measured in a Likert scale.	Time duration for this questionaire is 15 minutes. only one time point
Movement Assessment Battery for Children-2 (MABC-2)- general grade.	General grade of the subject's motor performance, that is measured in a ratio scale from the MABC-2.	Time duration for this test is 30 minutes. only one time point
Balance outcome of the Movement Assessment Battery for Children-2 (MABC-2).	Balance grade is measured in a ratio scale from the MABC-2.	Time duration for this test is 10 minutes. only one time point
Ball skills outcome of the Movement Assessment Battery for Children-2 (MABC-2).	Ball skills grade is measured in a ratio scale from the MABC-2.	Time duration for this test is 10 minutes. only one time point
Fine manual skills outcome of the Movement Assessment Battery for Children-2 (MABC-2).	Fine manual skills grade is measured in a ratio scale from the MABC-2.	Time duration for this test is 10 minutes. only one time point

Collaborators and Investigators

• Sponsor: Jay Zuckerman
• Investigators: Principal Investigator: jay zuckerman, DR, Israel: Clalit Health Services

Study record dates

Study Major Dates

• Study Start (Actual): December 5, 2017
• Primary Completion (Actual): January 1, 2019
• Study Completion (Actual): June 1, 2019

Study Registration Dates

• First Submitted: September 10, 2017
• First Submitted That Met QC Criteria: September 15, 2017
• First Posted (Actual): September 18, 2017

Study Record Updates

• Last Update Posted (Actual): April 2, 2020
• Last Update Submitted That Met QC Criteria: March 31, 2020
• Last Verified: March 1, 2020

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Mental Disorders; Neurodevelopmental Disorders; Motor Skills Disorders
• Other Study ID Numbers: MMC170038-17kCTIL

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Undecided

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No