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Clinical Trials in Turkey / NCT06967870
Starting soon Not applicable

The Effect of Cranial Osteopathy Intervention in Preterm Babies

NCT06967870 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-05-05
Last updated
2025-05-13

Condition(s) studied

OsteopathyPreTerm NeonateSensory ProfilesColicSleep QualityMotor Development of Premature Infants

Investigational drug(s) / intervention(s)

Osteopathic interventionHome based exercise education

Osteopathic intervention: Researcher will use osteopathic techniques on cranial area includes light touch. Home based exercises will be show on cases and demand to do exercise regularly

Home based exercise education: Home based exercises will be show on cases and demand to do exercise regularly.

Study summary

There are planing to have 2 groups of premature born cases. Each group will include 15 cases. Participants are need to be 28-37 weeks born and no older than post term 6 weeks. All cases are going to be evaluated. Home based exercise plan is going to be explained. The experimental group is going to take 6 osteopathic sessions weekly. After 6 weeks cases are going to be evaluated again.

Eligibility

Sex
ALL
Min age
1 Week
Max age
6 Weeks
Healthy volunteers
Accepted
Inclusion Criteria: * Premature birth (\<37 weeks) * Corrected age \<6 weeks. * Discharged to home * Stable condition * Family agrees to continue home program Exclusion Criteria: * Having a congenital cyanotic heart problem, * Being born earlier than 28 weeks, * The family not accepting to participate in the study, * Neglecting check-ups and sessions, * Using a respiratory appliance, * Presence of craniosynostosis, * Being included in another physiotherapy program during the study period

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bahriye Baş Bursa Osmangazi

More Abant Izzet Baysal University trials in Turkey

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06967870 on ClinicalTrials.gov ↗ ← All trials in Turkey