Actively Recruiting
RAdiology Consultation Effectiveness
Led by University Hospital, Montpellier · Updated on 2025-03-20
270
Participants Needed
1
Research Sites
133 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Performing a consultation with the radiologist before a spinal invasive procedure serves to foster a trusting physician-patient relationship. It also provides an opportunity for the comprehensive explanation of the procedure, its aftermath, and any patient inquiries. We believe that this proactive approach has the potential to alleviate pre-procedure anxiety, thereby contributing to an enhanced overall experience of the intervention and its outcomes. Despite these potential benefits, it is noteworthy that such consultations are not systematically implemented, and their impact on the intervention effictness remains unexplored in existing literature. The hypothesis is grounded in the belief that patients who perform a consultation preceding their spinal intervention are likely to witness improvements in both the overall experience of the procedure and its effectiveness.
CONDITIONS
Official Title
RAdiology Consultation Effectiveness
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient 18 years of age or older
- Referred to the imaging department for a peri-spinal injection under CT guidance
- Low back pain, dorsal pain, or neck pain with an average pain intensity of 65 5/10 on NPRS
You will not qualify if you...
- Patient unable to read and/or write French
- Patient unable to conduct a teleconsultation (no phone, no internet connection)
- Current pregnancy, breastfeeding, or lack of effective contraception for women of childbearing age
- Lack of consent
- Adults protected by law (guardianship, curatorship, or judicial protection)
- Non-emancipated minors
- Individuals unable to express consent (research conducted in emergency situations)
- Individuals deprived of liberty (by judicial or administrative decision, or involuntary hospitalization)
- Not affiliated with a social security scheme or not benefiting from such a scheme
- Participation in another research study with an ongoing exclusion period
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University Hospital of Montpellier
Montpellier, Occitnaie, France, 34295
Actively Recruiting
Research Team
M
Maxme PASTOR, MD
CONTACT
C
Catherine CYTEVAL, MD PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
3
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