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Effect of Trunk Support on Academic Engagement of Children With Severe Disability

Effect of Optimal Trunk Support on Academic Engagement of Children With Moderate to Severe Disability

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05391594
Enrollment
10
Registered
2022-05-26
Start date
2018-05-31
Completion date
2019-10-03
Last updated
2022-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy, Hypotonia, Metabolic Disease, Traumatic Brain Injury

Keywords

posture, trunk control, assistive device

Brief summary

This study evaluates the effect of optimizing trunk support based on segmental principles of trunk control, on academic engagement of children in academic settings.

Detailed description

Head and trunk posture control are foundational skills, impacting vision, communication, swallowing, eating, reaching, and gait. Vision, communication and upper extremity skills are critical for participation in educational settings. From an academic point of view, participants with poor trunk stability have difficulties staying erect and keeping their head and trunk steady. This interferes with concentration, reduces ability and aptitude for learning and can lead to fatigue and reduced time on task. Examination of the effect of optimal trunk support may yield critical information regarding academic engagement in children with moderate to severe disability. The investigators propose to facilitate use of a segmental approach by physical and occupational therapists in educational settings. Activities will include identifying level of trunk control and applying segmental principles to adapt participant's positioning devices for optimal function.

Interventions

DEVICEcustomized posture support

We will provide customized modifications for seated or standing or walking devices based on the child's segmental level of control

Sponsors

University of Hartford
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Single Subject Research Design

Eligibility

Sex/Gender
ALL
Age
3 Months to 21 Years
Healthy volunteers
No

Inclusion criteria

* Referral from physical, occupational or speech therapist working in Hartford Public School District or Connecticut Birth to Three, * Segmental deficit in trunk control as measured by Segmental Assessment of Trunk Control * parent or guardian consent that includes permission for video data collection and sharing of IEP (individualized education plan) or IFSP (individualized family support plan).

Exclusion criteria

* pain that interferes with positioning, * impending surgery that will result in extended absence from school

Design outcomes

Primary

MeasureTime frameDescription
Change in Video Behavior Coding of time on task for selected IEP or IFSP goals.On day 1 and one additional date at least 3 weeks later.Frequency and duration of 'on task' behavior will be coded for 2 or 3 of the child's existing education goals under two conditions, when child is in usual positioning equipment and in segmentally optimized equipment. Goals of interest reflect motor behaviors that promote task performance or interaction. These include 1) eye gaze (at people or objects), 2) reaching, 3) object manipulation, 4) head turning and 5) making choices (using eye gaze or reach).

Secondary

MeasureTime frameDescription
Change in vertical alignment of headOn the day 1 and one additional date at least 3 weeks later.frequency and duration of upright 'head position' will be coded for 2 or 3 of the child's existing education goals under two conditions, when child is in usual positioning equipment and in segmentally optimized equipment.
parent, teacher or aide device use recordfrom day 1 to second session at least 3 weeks later)frequency and duration of device use and comments about child and teachers response to using the device.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026