Actively Recruiting

Phase Not Applicable
Age: 20Years - 65Years
All Genders
Healthy Volunteers
NCT06554834

Effects of Osteopathic Technique on Autonomic Nervous System Activity

Led by SomaticMed · Updated on 2024-08-16

109

Participants Needed

1

Research Sites

20 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cranial osteopathic manipulation technique for brain and cranial nerve function, known as the fourth ventricle compression (CV4), has been recognized. Rib raising (RR), aimed at reducing rib restriction and conditions associated with sympathetic hypertonia, is also employed. This study aimed to assess, in about 109 healthy individuals, the effects of osteopathic techniques (CV4 and RR) on autonomic nervous system (ANS) activity, as measured by heart rate variability (HRV).

CONDITIONS

Official Title

Effects of Osteopathic Technique on Autonomic Nervous System Activity

Who Can Participate

Age: 20Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 20 and 60 years
  • Not currently undergoing any form of rehabilitation, physiotherapy, or osteopathy
Not Eligible

You will not qualify if you...

  • History of unstable arrhythmia or symptoms related to chest organs such as retrosternal pain or difficulty breathing
  • Pregnancy
  • Menstruation
  • Smoking
  • Symptoms suggesting bowel obstruction like bloating with pain, vomiting, or diarrhea
  • Previous surgical treatment in the head
  • Neurological diseases
  • Back or peripheral joint pain, trauma, or musculoskeletal dysfunction within the last 12 months
  • Physiotherapy or osteopathy treatment within the last month regardless of reason

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

SomaticMed

Wołomin, Prądzyńskiego, Poland, 05-200

Actively Recruiting

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Research Team

J

Jakub H Stępnik, MSc, D.O.

CONTACT

A

Agnieszka Kędra, Prof. Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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