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The Effects of Chiropractic Care in Children With Parent-reported Sensory Processing Disorder

The Effects of Chiropractic Care in Children With Parent-reported Sensory Processing Disorder: a Pilot Observational Study

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06413719
Enrollment
0
Registered
2024-05-14
Start date
2024-10-01
Completion date
2025-07-01
Last updated
2026-03-02

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

Conditions

Sensation Disorders

Keywords

Pediatrics, sensation disorders, autonomic nervous system, HRV, heart rate variability

Brief summary

This trial's main aims are to investigate the feasibility of implementing our novel assessment battery in tandem with normal and customary chiropractic care in a practice-based setting using a pediatric population with parent-reported SPD. More specifically, our primary endpoints are 1) recruitment rate, 2) tolerability, 3) adherence, 4) retention, 5) efficiency, and 6) data quality.

Detailed description

The total estimated time requirement for this study is \ 60 minutes. Up to 20 children (ages 5-12) will be recruited in a maximum 3-month enrollment period. The total estimated time requirement for the parent and child is \ 1 hour excluding the normal and customary chiropractic care. Per the clinic's normal and customary procedures, a welcome email is sent to each parent who schedules their child for a chiropractic exam at Premier Wellness Care (PWC) chiropractic (Crystal Lake, IL). An addendum will be added to this email briefly introducing the study along with a HIPAA compliant Jotform link to an online screening survey which incorporates the 38-item short sensory profile v1 (SSP-1). Those who complete the online screen and meet the eligibility criteria described below will be notified when they arrive at PWC for their initial exam & offered the opportunity to participate in the study. Informed consent (IC) and assent (IA) will be collected in a private room within PWC. A PWC staff member (TM) will sit down with each parent & child to review the IC & IA forms and answer any queries. To be enrolled, the parent must sign the IC and the child must acknowledge their willingness to participate verbally (e.g., "yes I would like to do the study") and/or physically (e.g., nod their head & give a 'thumbs up'). It will be made clear to all parents & children that they may decline participation without penalty and declining participation will in no way impact the child's access to normal and customary chiropractic care. Children will be asked to stand up straight on a scale so the investigators can measure their heights and weights. They will then be asked to sit in a comfortable chair, shown a visual analog scale (VAS), and asked to rate their pain level on a scale from 0 ("no pain") to 10 ("worst pain possible"). To track autonomic nervous system (ANS) activity, children will be asked to place their hand on the class II FDA registered neuroPULSE scanner (CLA Inc., Toronto, ON, Canada) and put their index, middle, & ring fingers onto the sensors. To track sweat gland (i.e., electrodermal, EDA) activity, a safe and unrecognizable low-voltage, high-amplitude current is passed between sensors located at the palmar-surfaces of the index and ring fingers. The pulse rate is measured via photoplethysmography (PPG) whereby blood flow-dependent changes in the quantity of emitted light passing though the fingertip are tracked via a sensor located on the palmar-surface of the middle finger. All signals will be transmitted to an iPad for viewing by the assessor via a secure Wi-Fi connection. With their hand in the neuroPULSE, children will undergo a sensory challenge protocol (SCP). For the SCP, the kids will be fitted with noise cancelling headphones and be shown a series of pictures. Prior to initiating the SCP, the assessor will instruct the child how to perform the test. The headphones will then be paired via Bluetooth to an iPhone/iPad device & switched on. Upon presentation of the "sitting" picture, the child will be asked to sit still and quietly for \ 2 minutes. Upon presentation of the "standing" picture, they will be asked to quickly stand and remain still and quiet for \ 2 minutes. Upon re-presentation of the "sitting" picture, the child will be asked to quickly return to a seated position & remain still and quiet for \ 2 minutes. Finally, upon presentation of the "noise" picture, the child will be asked to sit still and quietly while an auditory stimulus (1000 Hz, sine wave, 50% system volume, \ 75 dB) generated via a free tone generator app (f Generator, v7.4.1) is presented to both ears through the headphones for \ 2 minutes. The sound is like what someone would hear on your mobile device during an "AMBER Alert". This prolonged auditory stimulus is well below acceptable noise exposure limits and is in line with a protocol used in prior studies to test pediatric SPD populations. To help keep the children occupied during the SCP, a researcher will place an iPad directly in front of the subject & play a relaxing video (e.g., fish swimming in the ocean). When the SCP is finished, the video will be stopped, the headphones will be removed, and the child will be asked to remove his/her hand from the neuroPULSE scanner. During the child's assessment, parents will then be given an iPad & asked to complete the 38-item SSP-1. All assessments will be repeated following 12 sessions of PWC's normal and customary chiropractic care.

Interventions

None listed

Sponsors

Life University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
5 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* 5-12 years of age * SSP-1 total score no greater than 154

Exclusion criteria

* Unable to perform assessments due to vision, hearing, or movement impairment (e.g., blind, deaf, confined to wheelchair) * Unable to perform the assessments due to a preexisting condition whereby quick postural changes are contraindicated (e.g., postural orthostatic tachycardia syndrome (POTS), postural hypotension) * Pacemaker or known heart condition that influences the electrical or mechanical function of the heart

Design outcomes

Primary

MeasureTime frameDescription
Retention4 months (data collection period)% of participants completing the trial
Recruitment rate3 months (recruitment period)Average number of subjects enrolled per month
Proportion of participants able to complete assessments4 months (data collection period)Proportion of participants unable/unwilling to complete a given assessment as directed. This assesses 'Tolerability'.
Adherence4 months (data collection period)% of participants attending \<80% of their chiropractic sessions within the recommended time frame
Efficiency4 months (data collection period)Average time to completion of each assessment section
Data quality6 months (study period)% of acquisitions unsuitable for analysis for a given assessment

Contacts

PRINCIPAL_INVESTIGATORTyson Perez, DC, PhD

Life University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026