Ireland
--:--IST
Recruiting Not applicable

Evaluation of the Effect of Reiki on Pain After Spinal Fusion

NCT07062146 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-09-09
Last updated
2026-07-09

Condition(s) studied

Chirurgical Intervention

Investigational drug(s) / intervention(s)

reikiSham (No Treatment)

reiki: Reiki sessions for 30 minutes, on Day-7 before the surgery and on D15 after the surgery

Sham (No Treatment): Sham sessions for 30 minutes, on D-7 before the surgery and on D15 after the surgery,

Study summary

This study involves patients undergoing lumbar spine surgery (lumbar arthrodesis). It compares the effects of Reiki, an energy-based therapy, with conventional approaches to relieve postoperative pain.

The goal is to determine whether this non-drug method can help reduce pain, limit the use of painkillers, and enhance patient comfort during recovery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * \- Subject aged 18 years or older; * Referred for a lumbar fusion of up to 3 levels. * Absence of participation in another clinical study. * Subject affiliated with a social security scheme or beneficiary of such a scheme Exclusion Criteria: * Neuropathic patient * Presence of neuropathic pain * Diagnosis of fibromyalgia * Received therapeutic touch, polarity therapy, or professional massage therapy in the past four weeks * Unable to undergo medical follow-up for the study * Adult subject protected by law, under guardianship or trusteeship

Primary outcome measure(s)

  • pain will be assessed at Day 15 using the VAS ( Visial Analog Scale) — DAY 15
    The Visual Analog Scale is a subjective measurement tool commonly used to assess the intensity of pain. It consists of a horizontal 10-centimeter line on which the patient marks a point that reflects their experience. Minimum and maximum values: 0 = complete absence of the symptom 10 = the most severe imaginable intensity of the symptom Score interpretation: Higher scores indicate greater symptom intensity Lower scores indicate lesser intensity

Trial sites (1)

FacilityCityRegionStatus
Clinique Bizet Paris France Recruiting
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 NCT07062146 on ClinicalTrials.gov ↗ ← All trials in France