Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05825248
Other study ID # H.Miller.2.27.23
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date April 10, 2023
Est. completion date June 15, 2023

Study information

Verified date April 2023
Source Salus University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this quantitative experimental study is to compare two occupational therapy interventions intended to improve functional skills. The main questions it aims to answer are: Question 1: Do preschool children who participate in occupational therapy intervention designed to promote integration of the TLR reflex in conjunction with fine and gross motor intervention demonstrate improved integration of the TLR reflex in clinical assessment, compared to children who participate in fine and gross motor intervention only for an equal amount of time? Question 2: Do preschool children who participate in occupational therapy intervention designed to promote integration of the TLR reflex in conjunction with fine and gross motor intervention demonstrate improved integration of the TLR reflex in clinical assessment, compared to children who participate in fine and gross motor intervention only for an equal amount of time? Participants will participate in either a therapy program consisting of either fine and gross motor treatment in conjunction with reflex integration treatment, or fine and gross motor treatment only. If there is a comparison group: Researchers will compare the group recieving reflex integration in conjunction with fine and gross motor treatment and the fine and gross motor only group to see if one is more effective at integrating the reflex and/or improving functional skills.


Description:

Pre-intervention, INPP screening for TLR will be administered to determine eligibility for the study and baseline of reflex persistence. the Peabody Developmental Motor Scales 2nd Edition (PDMS2) stationary and visual motor integration sections will be administered to assess fine and gross motor skills. Stratified random sampling will be used to create two parallel groups. Both the INPP and PDMS2 will be administered and scored by a masked examiner who is licensed to practice occupational therapy. For 6 weeks, one group will receive 20 minutes standard occupational therapy intervention while the second group will receive 10 minutes of standard occupational therapy intervention and 10 minutes of TLR integration protocol (Move Play Thrive Program). 20 minutes per week is standard treatment time for preschool occupational therapy sessions in Aberdeen School District. Intervention will be provided by the PI, Healey Miller. Post-intervention, the Peabody Developmental Motor Scales 2nd Edition (PDMS2) stationary and visual motor integration sections will be re-administered to assess fine and gross motor skills and the INPP screening for TLR will be re-administered to assess for retained TLR reflex. Both the INPP and PDMS2 will be administered and scored by a masked examiner who is licensed to practice occupational therapy. Data will be reviewed to determine if the progress made between groups, in regard to motor skills and reflex integration, is statistically significant. Data will be reviewed to compare progress made in each group in fine/gross motor skills and reflex integration, and to determine if changes made are statistically significant.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 23
Est. completion date June 15, 2023
Est. primary completion date June 15, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 3 Years to 6 Years
Eligibility Inclusion Criteria: - 3 to <6 years old - Attending preschool at Hopkins Preschool, Stevens Elementary Preschool, or Central Park Preschool within Aberdeen School District - Receiving weekly occupational therapy services to address fine motor, gross motor, or sensory deficits - Displays signs of retained tonic labyrinthine reflex (TLR) after a brief INNP TLR screening test (a score of 3, or 4 will be considered a retained TLR for the purpose of this study) Exclusion Criteria: - Students enrolled in an alternative enrollment format - Students who are absent for a consecutive period of 5 or more school days

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Fine and gross motor treatment only
occupational therapy intervention involving general fine and gross motor activities
Reflex integration + fine and gross motor treatment
occupational therapy intervention involving general fine and gross motor activities as well as targeted reflex integration exercises

Locations

Country Name City State
United States Aberdeen School District Aberdeen Washington

Sponsors (1)

Lead Sponsor Collaborator
Salus University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline functional skills at 8 weeks functional skills as measured by the Peabody Developmental Motor Scales Stationary and Visual Motor Integration sections. This standardized test scoring can be converted into z-scores for data comparison. week 0 and week 8
Primary Change from baseline TLR inegration at 9 weeks integration of the tonic labyrinthine reflex as measured by the INPP measure for retained primitive reflexes. INPP scale 0-4, 0 being no reflex retained and 4 being severe reflex retention week 0 and week 8
See also
  Status Clinical Trial Phase
Completed NCT06052410 - Early Intervention in Children at Risk of Developmental Delay N/A
Recruiting NCT04518332 - Intraoperative Cerebral and Renal Tissue Oxygen Saturation and Pediatric Living Donor Liver Transplantation Prognosis.
Active, not recruiting NCT02000284 - Mitochondrial Dysfunction in Autism Spectrum Disorder
Recruiting NCT05527080 - Development of Motility and Cognition in Infants
Recruiting NCT04672967 - MAP Autism Prediction Study
Completed NCT02712853 - Improving Autism Screening With Brain-Related miRNA
Completed NCT01975506 - Occupational Therapy in the Context of Head Start N/A
Completed NCT01253083 - Mobility Training to Improve Motor Behavior in Toddlers With or at Risk for Cerebral Palsy: A Pilot Study Phase 1
Not yet recruiting NCT05605977 - Home-based Visual-motor Training Program on Kindergarteners N/A
Completed NCT05408351 - The Indonesian Version of Ages and Stages Questionnaire III Accuracy Compared to Bayley Scales of Infant Development III
Completed NCT02832557 - A Salivary miRNA Diagnostic Test for Autism
Recruiting NCT02769949 - Pediatric Patients With Metabolic or Other Genetic Disorders
Active, not recruiting NCT02813889 - SmarToyGym: Smart Detection of Atypical Toy-oriented Actions in At-risk Infants N/A
Completed NCT01351077 - CHICA Developmental Screening Study N/A
Completed NCT02115334 - Development and Effectiveness of Home-based Programs for Preschool Children With Developmental Delay N/A
Suspended NCT03307317 - Mirror Neuron Network Dysfunction as an Early Biomarker of Neurodevelopmental Disorder
Completed NCT03223688 - Early Intervention for Developmental Delay N/A
Completed NCT02141802 - Clinical Effectiveness of Increased Standing Time in Non-ambulant Children With Cerebral Palsy:a Pilot Study N/A
Completed NCT03847337 - Can Novel Telemedicine Tools Reduce Disparities Related to Early Identification of Autism N/A
Recruiting NCT05675371 - Treatment Monitoring in Autism Spectrum Disorder (ASD) in Children