The Benefits of Massage for Back Pain
Effect of Directed Massage in Patients Suffering From Chronic Spinal Pain Refractory to PO2S: a Randomised Clinical Trial
1 other identifier
interventional
50
1 country
1
Brief Summary
This study evaluates the effectiveness of a oriented massage by comparing it with that of a classic symmetrical massage.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable chronic-pain
Started Jan 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 24, 2024
CompletedStudy Start
First participant enrolled
January 15, 2025
CompletedFirst Posted
Study publicly available on registry
June 24, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 15, 2026
June 24, 2026
August 1, 2025
1.7 years
August 24, 2024
June 18, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Change in Pain Intensity on the 0-to-10 Numeric Pain Rating Scale
Pain intensity will be assessed using the 0-to-10 Numeric Pain Rating Scale, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity. The outcome measure is the change in pain intensity score from immediately before each treatment session to 24 hours after the same treatment session.
Day 0 immediately before treatment Session 1, Day 1 at 24 hours after treatment Session 1, Day 7 immediately before treatment Session 2, and Day 8 at 24 hours after treatment Session 2
Study Arms (2)
Oriented massage
EXPERIMENTALPatients receive a oriented massage based on their Specific Torsion Pattern (STP)
Symmetrical massage
ACTIVE COMPARATORPatients receive a symmetrical massage
Interventions
Eligibility Criteria
You may qualify if:
- Patients suffering from chronic spinal pain (for at least 3 months) refractory to PO2S
- Patients aged between 18 and 80
- Patients having been treated with PO2S and still suffering from refractory pain
- Patients who gave informed consent to participate in the study
You may not qualify if:
- Patients whose chronic spinal pain is caused by inflammatory disease, tumour, infection or trauma to the back.
- Patients with a history of back surgery and/or vertebral fracture in the last 6 months
- Patients with a motor disability related to the reason for consultation
- Women who are more than six months pregnant.
- Patients who are unable to communicate or understand the study process.
- Patients who had been assessed and excluded by Dr Jean Luc Isambert.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cabinet d'ostéopathie
Noumea, Sud, 98800, New Caledonia
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- COMichelBoeuf
Study Record Dates
First Submitted
August 24, 2024
First Posted
June 24, 2026
Study Start
January 15, 2025
Primary Completion (Estimated)
September 15, 2026
Study Completion (Estimated)
October 15, 2026
Last Updated
June 24, 2026
Record last verified: 2025-08