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Motor DevelopmentNCT03999619

Evaluation of the Move 2 Learn (M2L) Program for Young Children

A study testing Move 2 Learn in people with Motor Development and Physical Activity, run by University of Toronto at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Move 2 Learn (M2L) is a 10-week movement and pre-literacy program for preschool aged children and their parents designed to improve both movement and reading skills as well as support their overall cognitive, physical, and psychological development. Read more about this study

Who is it for?
Ages 3 to 4 yearsHealthy volunteers can take part
Conditions the study is for
Motor Development, Physical Activity
What is being tested?
Move 2 Learn
Could I receive a placebo?
No, everyone receives an active treatment
How many people
32 participants
Where
1 siteCanada
Study dates
7 Jan 2019to 31 Jan 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 to 4 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Between the ages of 3 and 4 years with typical development

Who cannot join

  • Developmental delay
  • Physical conditions that prohibit safe participation in physical activity

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • University of Toronto

    Toronto, Ontario, M5S 2W6

Other trials in Canada

About this study

Official title: Evaluation of the Move 2 Learn (M2L) Program for Young Children: A Randomized Wait-list Controlled Trial

Move 2 Learn (M2L) is a 10-week movement and pre-literacy program for preschool aged children and their parents designed to improve both movement and reading skills as well as support their overall cognitive, physical, and psychological development. This study will be using a randomized wait-list controlled trial design to evaluate the program on several outcomes: motor skills, pre-literacy skills, cognitive function, perceived physical competence, and physical activity. Children ages 3 to 4 years with typical development will be randomized to either start the program immediately or enter the wait-list control group to begin the program after a 10-week control period. The outcomes will be assessed for all children three times, at week 0, week 11, and week 21 to evaluate change over time in both groups.

Read the detailed description

Design: The study will use a randomized wait-list controlled design. Children will be randomized to either the intervention arm or the wait-list control arm with a 1:1 ratio. Children randomized to the intervention arm will enter the Move 2 Learn (M2L) intervention during the first 10-12 weeks of the study period; children randomized to the wait-list control arm will not receive any intervention during the first 10-12 weeks of the study (the wait-list control period), then will enter into a modified M2L intervention during the second 10 to 12 weeks of the study. All children will be assessed 3 times at 10-12-week intervals. The intervention arm will be assessed before and immediately after they receive the intervention, and at a 10-12-week follow-up. The wait-list control group will be assessed at baseline, immediately before receiving the intervention (10-12 weeks following) and after they receive the intervention.

Children will be randomized 1:1 to either the intervention or wait-list control group. Simple randomization will be completed using a computer algorithm. After confirming eligibility and obtaining verbal consent, a research assistant will send the complete list of study IDs to an independent biostatistician who will use a computer algorithm to randomly assign the child to the intervention or to the wait-list control group. Sealed, opaque, and numbered envelops will be prepared with their allocation details (e.g. if randomized to the intervention arm, information regarding the location and time of the intervention will be provided).

Intervention: The Move 2 Learn (M2L) program (both the original and the modified program) will be run out of the gym space provided in-kind by the Faculty of Kinesiology and Physical Education at the University of Toronto. This behavioral program will run for 60 minutes once per week for 10 consecutive weeks and will consist of three components: direct movement skill instruction, unstructured exploratory free-play, and in interactive storybook reading activity. There is active involvement of at least one parent/caregiver in the direct instruction and reading components and parents/caregivers are provided with handouts outlining specific strategies to implement for at-home practice of the activities. Each week, parents will be verbally encouraged to practice these skills at home with their parents.

The participants randomized to the wait-list control group will not receive any intervention during the control period (between time 1 and time 2 assessments. After their time 2 assessment is complete, participants will receive a modified version of the M2L program. All in-sessions components of the M2L program will be implemented with the exception of the parent handouts and the verbal encouragement to practice at-home between sessions Assessments: At the time 1 appointment, children will be administered the gross motor subscales of the Peabody Developmental Motor Scales-2 (PDMS-2; Folio \& Fewell, 2000), the perceived physical competence subscale of the Pictorial Scale (PPC) of Perceived Competence and Social Acceptance for Young Children-Preschool-Kindergarten version (PSCS-PK; Harter \& Pike, 1984), the Phonological Awareness Literacy Screening: Preschool (PALS-PK; Invernizzi, Sullivan, Meier, \& Swank, 2004), the Preschool Word and Print Awareness Test (PWPA; Justice \& Ezell, 2002), and the Picture Deletion Task for Preschoolers (PDTP; Byrne, DeWolfe, \& Bawden, 1998; Corkum, Byrne, \& Ellsworth, 1995). Parents will complete a demographic questionnaire (see Demographic Survey for Parents), and a parental engagement questionnaire that asks about the use of specific activities to promote motor skill and early literacy skill development (see Parental Engagement Survey) and the Behaviour Rating Inventory of Executive Function®-Preschool Version (BRIEF-P; Gioia, Espy, \& Isquith, 2001). On completion of testing, children will be fitted with an accelerometer; parents will be instructed on its proper use and provided with a diary to track wear time (e.g., time of day put on, time of day removed). After 7 days, parents will mail back the the accelerometer(s) and diary (see Accelerometer Log). At each subsequent appointment (time 2 and time 3), all outcomes described above will be measured again (see Figure 2) except for the parent demographic survey and the BRIEF-P. Each study appointment will take approximately 1.5 hours.

All outcomes will be assessed at the INfant and Child Health (INCH) Lab at the University of Toronto by trained graduate students, blind to the intervention status of the participants.

Measures: The primary outcomes include fundamental movement skills and pre-literacy skills. Movement skills will be assessed using the gross motor sub-scales of the Peabody Developmental Motor Scales - 2 (PDMS-2). The Preschool Word and Print Awareness Test (PWPA) and the Phonological Awareness Literacy Screening: Preschool (PALS-PK) to measure print-concept knowledge and alphabet knowledge, respectively. Secondary outcomes include physical activity, cognitive function, and self-perceived physical competence. All outcomes will be assessed at the INfant and Child Health (INCH) Lab at the University of Toronto by trained graduate students, blind to the intervention status of the participants.

Motor Skill Proficiency: The gross motor subscales of the PDMS-2 (stationary performances, locomotion, and object manipulation) will be used to assess change in motor skill over the course of the study and will be administered by a trained graduate student blind to the intervention status of the participant. This tool is commercially available.

Pre-literacy Skills: Emergent literacy skills that will be measured include print concepts and alphabet knowledge. The PALS-PK Upper-case Alphabet Recognition task will be used to measure children's alphabet knowledge. This tool is commercially available. Print awareness will be assessed using the PWPA. The assessment uses an interactive story book reading activity to test children on their knowledge of 14 print concepts, such as print directionality and print function (Justice \& Ezell, 2002). This tool is freely available as it was published as an appendix in the Justice, Bowles, \& Skibbe, 2006 article.

Physical Activity: Accelerometry is an objective method of assessing free-moving physical activity, and is the method best-suited to measuring activity in young children. This study will use the Actigraph GT3X activity monitor, a light (27g) and small (3.8cm × 3.7cm × 1.8cm) device, secured to the child by a belt worn around the waist. A 3 s epoch will be used (Obeid, Nguyen, Gabel, \& Timmons, 2011) and will record physical activity for 7 consecutive days (Trost, Pate, Freedson, Sallis, \& Taylor, 2000).

Executive Function: The BRIEF-P, a parent-report tool, will be used to assess children's trait executive function at week 0 (Sherman \& Brooks, 2010). State executive function will be assessed using the Attention Sustained subtest 6 of the Leiter-3 test battery. The task requires children to view a target image (an animal) and identify the images that match among a set of distractor images as quickly as possible; there are 4 trials, each of which have a practice set. This tool is commercially available. To assess inhibition, the Head Toes Knees and Shoulders instrument will also be administered. This task requires Children are to play a game in which they must do the opposite of what the experimenter says. The experimenter instructs children to touch their head (or their toes), but instead of following the command, the children are supposed to do the opposite and touch their toes.

Perceived Physical Competence: The PSCS-PK will be used to assess each child's level of perceived competence. There are physical competence subscale (6-items) will be administered. The scale is an extension of Harter's Perceived Competence Scale for Children (1982). This tool is freely available online.

Demographic Factors: The baseline questionnaire will include questions about the parent and the child on age, gender, race/ethnicity, parental education and occupation, and household income. The questionnaire will be parent-completed.

Parental Engagement: Parents will be asked about the use and the frequency of use, of specific activities that will be employed in our program. A parent-reported questionnaire specific to these activities has been created to determine if parents have been using these strategies before our program, and if they have incorporated them into their activities with their child after having completed the program.

Parental Acceptability: Consenting parents will engage in a focus group, led by a facilitator. Staying consistent with the unstructured nature of a focus group, open-ended questions designed to initiate discussions surrounding their attitudes and opinions, likes and dislikes of the program will be asked. The discussion will be audio recorded and transcribed verbatim. Focus group transcriptions will be used to revise the program and its components to better serve the community.

Analysis: Basic descriptive statistics of participating children and parents will be completed. Mixed effects models will be used to assess a group-by-time effect on all outcomes. All analyses will be conducted on an intention to treat basis.

Being tested
Move 2 Learn
Keywords
Pre-Literacy Skills
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Move 2 LearnBehavioural

    Also called M2L

    10-week (1 hour/week) program designed to target fundamental movement and pre-literacy skills with active parent involvement.

Study groups in NCT03999619
Study groupRoleWhat they receive
ExperimentalExperimentalChildren will enter into the Move 2 Learn program immediately following their first assessment (between week 0 to 10)
Receives: Behavioral: Move 2 Learn
Wait-list ControlOtherChildren will not participate in the program until after their second assessment (between week 11 to 21). Their control period will take place between week 0 and 10.
Receives: Behavioral: Move 2 Learn

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Motor skills

    Movement skill competency (Peabody Developmental Motor Scales- 2nd ed; total gross motor scores range from 0 to 286 with higher scores representing higher motor skill)

    Measured: Change from week 0 to 11

  2. Change in Pre-literacy skills

    Print Concept Knowledge (Preschool Word and Print Awareness Tool; standardized scores range from 0 to 181 with higher scores representing higher pre-literacy skill)

    Measured: Change from week 0 to 11

Secondary outcomes (14)
  1. Change in Perceived Physical Competence

    Perceptions of one's own physical abilities (Physical Competence subscale of Harter's Pictorial Scale of Perceived Competence and Social Acceptance for Young Children; subscale scores range from 4 to 24 and will be averaged to produce a score ranging from 1 to 4 with higher scores representing more positive self perceptions)

    Measured: Change from week 0 to 11

  2. Change in Perceived Physical Competence

    Perceptions of one's own physical abilities (Physical Competence subscale of Harter's Pictorial Scale of Perceived Competence and Social Acceptance for Young Children; subscale scores range from 4 to 24 and will be averaged to produce a score ranging from 1 to 4 with higher scores representing more positive self perceptions)

    Measured: Change from week 11 to 21

  3. Change in Executive function - Attention

    Sustained Attention (Subtest 6 of the Leiter-3; scores of correct responses range from 0 to 70 with high scores representing higher levels of attention; scores of errors of commission range from 0 to 205 with higher scores representing lower levels attention)

    Measured: Change from week 0 to 11

  4. Change in Executive function - Attention

    Sustained Attention (Subtest 6 of the Leiter-3; scores of correct response range from 0 to 70 with high scores representing higher levels of attention; scores of errors of commission range from 0 to 205 with higher scores representing lower levels of attention)

    Measured: Change from week 11 to 21

  5. Executive function - Inhibition

    Inhibition (Head Toes Knees Shoulders Instrument; scores range from 0 to 52 with higher score representing higher inhibition)

    Measured: Change from week 0 to 11

  6. Executive function - Inhibition

    Inhibition (Head Toes Knees Shoulders Instrument; scores range from 0 to 52 with higher score representing higher inhibition)

    Measured: Change from week 11 to 21

  7. Physical activity

    Levels of physical activity over 7 days as measured using accelerometers

    Measured: Change from week 0 to 11

  8. Physical activity

    Levels of physical activity over 7 days as measured using accelerometers

    Measured: Change from week 11 to 21

  9. Parental engagement - movement activity

    Parent-reported levels of engagement in completing movement activities at home

    Measured: Change from week 0 to 11

  10. Parental engagement - movement activity

    Parent-reported levels of engagement in completing movement activities at home

    Measured: Change from week 11 to 21

  11. Parental engagement - reading activity

    Parent-reported levels of engagement in completing pre-literacy activities at home

    Measured: Change from week 0 to 11

  12. Parental engagement - reading activity

    Parent-reported levels of engagement in completing pre-literacy activities at home

    Measured: Change from week 11 to 21

  13. Change in Motor skills

    Movement skill competency (Peabody Developmental Motor Scales- 2nd ed; total gross motor scores range from 0 to 286 with higher scores representing higher motor skill)

    Measured: Change from week 11 to 21

  14. Change in Pre-literacy skills

    Print Concept Knowledge (Preschool Word and Print Awareness Tool; standardized scores range from 0 to 181 with higher scores representing higher pre-literacy skill)

    Measured: Change from week 11 to 21

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2019
  2. Study start7 Jan 2019
  3. Primary completion31 Jan 2020
  4. Study completion31 Jan 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized Wait-list Controlled Design
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
32 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03999619
Sponsor's protocol ID
8303
Status last verified
Dec 2020
First submitted
12 Jun 2019
Last updated
19 Dec 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Move 2 Learn in people with Motor Development and Physical Activity, run by University of Toronto at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Motor skills (time frame: Change from week 0 to 11). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Dec 2020; AzTrials last refreshed its copy on 27 Oct 2026.

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