Spinal manipulation on heart rate variability in children with cerebral palsy
Official title: The Effect of Spinal Manipulation on Heart Rate Variability in Children With Cerebral Palsy. Randomised Comtrolled Trial
Run by International Clinic of Rehabilitation, Ukraine · NCT07504640 · Data updated 2026-11-12
This study will test whether spinal manipulation changes heart rate variability in children with cerebral palsy, using a crossover design where each child receives both real and sham procedures on different days.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 4 Years to 18 Years |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | International Clinic of Rehabilitation, Ukraine Academic / other |
| Locations | 1 site (Lviv) |
| Status | Recruiting |
| Started | May 1, 2026 |
| Main results expected | October 1, 2026 |
| Study ends | November 1, 2026 |
| Registry record updated | May 29, 2026 |
| Trial ID | NCT07504640 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Children with cerebral palsy, GMFCS levels I–III, who can cooperate with study procedures.
✕Probably not a fit
Children who are non-cooperative, have hyperkinetic CP, or take medications impacting autonomic regulation may not benefit from this trial.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, sham-controlled crossover trial investigates the immediate effect of spinal manipulation on heart rate variability in children with cerebral palsy. Each participant undergoes four sessions on separate days, with two sessions containing spinal manipulation and two with a sham procedure in random order. Heart rate variability, particularly RMSSD, is measured before and after each intervention under standardized conditions to assess autonomic nervous system changes. The crossover design allows each child to serve as their own control, reducing variability and focusing on acute autonomic responses to the intervention.
Why it matters
Potential benefit: If successful, the approach could reveal a non-pharmacologic means to influence autonomic function in CP, potentially informing supportive therapies.
How similar studies have gone: Previous studies in related therapies have shown mixed or exploratory results; this trial tests a novel application in CP using a crossover design.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Cerebral palsy * Motor function levels I-III according to GMFCS * Cooperative behavior Exclusion Criteria: * Hyperkinetic forms * Use of medications affecting autonomic regulation
Where it's running
-
Elita Rehabilitation Center
Lviv, Ukraine Recruiting
Study contacts
- Study coordinator: Oleh Kachmar, MD, PhD
- Email: okachmar@ic.reha.lviv.ua
- Phone: 00380673537927
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.