About this trial
The goal of this crossover randomized clinical trial is to assess the effects of osteopathic manipulative treatment (OMT) compared to standard of care repositioning in children diagnosed with positional/deformational plagiocephaly. The main hypothesis is that children who received OMT will show significantly improved anthropometric measures of cranial symmetry over those receiving the current pediatric standard of care of repositioning.
This is a two-arm, randomized cross-over clinical trial. With parental consent, pediatric patients (infants \<4 months of age) will be organized into one of two groups:
1. Those who receive OMT with emphasis on osteopathic cranial manipulative medicine (OCMM) to restore cranial symmetry. 2. Those who receive standard care only with repositioning attention from the parents After 8-weeks of being in the first group, each participant will cross-over into the second group (OMT or repositioning) N = 122 subjects diagnosed with deformational plagiocephaly (DP) are to be recruited (to allow for natural attrition and loss to follow up) with the recruitment to continue until 61 patients have been placed in each of the two groups and will cross-over to the respective treatment group (OMT and standard of care repositioning therapy).
Timeline: It is projected that to recruit and carry out the assessments and interventions (8-weeks of each group with 12-months of follow-up longitudinally), it will require two years (24-months) from the beginning of the study to completion.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Diagnosed with positional plagiocephaly
Under 4-months of age (between birth - 4 months) at the time of enrollment
Preterm birth (<37 weeks)
Genetic syndromes
Disqualifiers
None
Trial design
Crossover
Treatments tested in this trial
Osteopathic Manipulative Treatment
Procedure/SurgeryOsteopathic Manipulative Treatment is a manual treatment therapy applied by licensed physicians that consists of using ones hands to improve the structure and function of the body. In this situation it will involve gentle and passive modalities that are well-tolerated by infants.
Standard of Care Repositioning
BehavioralParents will receive standardized handouts/materials instructing on repositioning intended to help improve head shape in infants with plagiocephaly.
Treatment groups
Trial outcomes
Primary outcomes
Cranial Vault Asymmetry Index
Anthropometric measurement of cranial asymmetry
Head circumference
Standard growth parameter measured in infants
Weight
Standard growth parameter measured in infants
Secondary outcomes
Medical history
Patients charts will be reviewed after first year of life to assess for medical issues including otitis media, developmental delay, allergic rhinitis, vision problems, torticollis, hospitalizations, need for a helmet to treat plagiocephaly, colic, reflux/GER, etc.
Developmental Milestones
Patients' enrolled in the study will have developmental stones monitored as per general pediatrician's protocol to screen for developmental delays.
Sponsors and contacts
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