RecruitingNot ApplicableNCT06802120

Effects of Osteopathic Management on Disability and Quality of Life After Lumbar Arthrodesis

Effects of Osteopathic Management on Disability and Quality of Life After Lumbar Arthrodesis. A PARALLEL, RANDOMIZED AND DOUBLE-BLIND CONTROLLED PILOT STUDY


Sponsor

Clinique Bizet

Enrollment

40 participants

Start Date

Jan 2, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The aim of our study is to assess the effect of a combined physiotherapy and osteopathy treatment versus a placebo on the management of disability and quality of life after lumbar arthrodesis. This study will provide a better assessment of the use of osteopathy as a non pharmacological approach to post-operative management. For this purpose, We will analyze the effects of these two approaches, targeted and non-targeted osteopathy (TO vs. NTO), on patients' disability and quality of life after surgery.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying osteopathy real and sham osteopathy for people with chirurgical intervention. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERosteopathy real

treatment with real osteopathy 2 times a week for 8 weeks

OTHERsham osteopathy

treatment with sham osteopathy 2 times a week for 8 weeks


Locations(1)

Clinique Bizet

Paris, France

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NCT06802120


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