Well Adjusted Students
Chippewa Falls, Wisconsin, 54729, United States
NCT Number: NCT07256327
The main aim of this pilot observational study is 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 sensory processing disorder (SPD). The secondary aim is to assess potential changes in objective and subjective outcomes.
Trial opening soon.
Get Notified5 year–12 year
All sexes
Observational
Chippewa Falls, Wisconsin, 54729, United States
Twenty (20) parents & children with probable or definite parent-reported SPD as determined by the Short Sensory Profile (SSP) will be enrolled. The primary outcomes are 1) eligibility, 2) tolerability, 3) adherence, and 4) retention. The secondary aim is to assess the potential effects of subluxation-based pediatric chiropractic care on electrocardiography (ECG)-derived heart rate variability (HRV) and parent-reported outcomes (PROs). Results from this study will inform the feasibility of a larger study powered to assess the effectiveness of pediatric chiropractic care on clinical outcomes in a pediatric population with SPD.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: From enrollment to baseline SSP score evaluation (up to 1 hour)
The number of enrollees (i.e., participants who consent/assent) who score ≤154 on the baseline Short Sensory Profile (SSP), divided by the total number of enrollees. This assesses 'Eligibility'.
Time frame: From enrollment to baseline assessment completion (up to 1 hour)
The number of participants able to complete all baseline assessments as directed, divided by the total number of participants. This assesses 'Tolerability'.
Time frame: From enrollment to the end of participation (up to 10 weeks)
The number of participants attending 15 sessions of chiropractic care within 10 weeks, divided by the total number of participants. This assesses 'Adherence'.
Time frame: From enrollment to the end of the 10 week study period.
The number of participants attending the 3rd and final assessment session, divided by the total number of participants. This assesses 'Retention'.
Time frame: From enrollment to the end of participation (up to 10 weeks)
Change in resting-state heart rate variability (HRV) from baseline. Children will undertake 3 minutes of electrocardiography (ECG) while seated. ECG data will be used to derive HRV (i.e., RMSSD).
Time frame: From enrollment to the end of participation (up to 10 weeks)
Change in SSP scores from baseline. The SSP is a 38-item parent-report designed to assess a child's responsiveness to sensory stimuli including tactile sensitivity, taste/smell sensitivity, and visual/auditory sensitivity.
Time frame: From enrollment to the end of participation (up to 10 weeks)
Change in PASS scores from baseline. The PASS is an 80-item parent-report questionnaire designed to assess autonomic function in children across four main subscales: 1) mood, behavior, and emotion; 2) secretomotor/sensory integration; 3) urinary/gastrointestinal systems; 4) circulation, thermoregulation, sleep, and breathing.
Contact information is provided by the study sponsor or research team.
Life University
Other
The Effects of Chiropractic on Kids With Sensory Processing Challenges: a Pilot Observational Study
Acronym: SPD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07656961
Mental Disorders, Neurodevelomental Disorders
Istanbul, Ataşehir, Turkey (Türkiye)
View Trial DetailsNCT07493096
22q11 Deletion Syndrome, 22q11.2 Deletion Syndrome
The Woodlands, Texas, United States
View Trial DetailsNCT05217199
Communication Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Kahramanmaraş, Dulkadiroglu, Turkey (Türkiye)
View Trial DetailsNCT07729800
Brain Damage, Chronic, Brain Diseases
Lahore, Pakistan
View Trial Details