See if athletes who've had cervical spine surgery can safely return to sport based on new functional tests
Official title: Evaluation of the Statistical Validity of Cervical Spine Measurements-Including Range of Motion, Strength, and Functional Test Results-for Return to Sport in Patients Who Have Undergone Surgery for Cervical Stenosis and/or Herniation : Comparison Between a Group of Patients and a Group of Healthy Controls
Run by GCS Ramsay Santé pour l'Enseignement et la Recherche · NCT07886112 · Data updated 2026-11-12
This study tests whether specific physical tests and questionnaires can reliably indicate when athletes who had cervical spine surgery can safely return to sport.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 40 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | GCS Ramsay Santé pour l'Enseignement et la Recherche Academic / other |
| Locations | 1 site (Lyon) |
| Status | Recruiting |
| Started | July 19, 2022 |
| Main results expected | November 20, 2026 |
| Study ends | December 20, 2026 |
| Registry record updated | October 21, 2026 |
| Trial ID | NCT07886112 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal participants are 18-40 years old, actively participate in sports at least weekly, have undergone cervical spine surgery (fusion, arthrodesis, disc replacement, or foraminotomy), and are assessed by their surgeon to be eligible.
✕Probably not a fit
Patients with non-sporting activity levels, different surgical histories, or non-surgical management may not benefit from these specific return-to-sport benchmarks.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial focuses on athletes aged 18-40 who had cervical stenosis or related surgery and compares them to athletes without neck problems. It uses patient-reported questionnaires and physical tests to measure range of motion, strength, and functional performance after surgery. The goal is to identify a clear, functional benchmark that helps determine a safe return-to-play timeline. The study is conducted at a Lyon, France hospital and is led by a European surgical and research institution. Interventions involve standardized questionnaires and physical assessments rather than a drug or device trial.
Why it matters
Potential benefit: If successful, clinicians may have a validated set of tests to guide return-to-sport decisions after cervical spine surgery.
How similar studies have gone: Previous studies have explored return-to-work and general functional recovery, but this trial adopts a focused approach on sport-specific functional recovery after cervical spine surgery.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient group Patients meeting all the following criteria will be included: * Male or female aged 18 to 40 years * Injury requiring surgery sustained during a sports activity * Participation in sports activity at least once a week * Cervical spine arthrodesis, cervical disc replacement, and/or foraminotomy * Surgery performed by surgeons at the Centre Orthopédique Santy (Lyon) * Inclusion based on the surgeon's decision during the 45-day post-operative visit Control group Participants meeting all the following criteria will be included: * Male or female aged 18 to 40 years * Participation in sports activity at least once a week * No history of cervical pathology * No history of surgery involving the shoulder girdle * No neck pain in the month prior to the test In both groups o Patient having signed an informed consent form Subject affiliated with or a beneficiary of a social security scheme Exclusion Criteria: Patient group Patients meeting any of the following criteria will be excluded: o Medical contraindication Control group Participants meeting any of the following criteria will be excluded: * Reported history of spinal or upper-limb injury within the last 12 months * Reported history of upper-limb surgery In all cases, the following will be excluded: * Protected individuals: adults under guardianship, curatorship, or other legal protection; individuals deprived of liberty by judicial or administrative decision * Pregnant, breastfeeding, or recently delivered women
Where it's running
-
Hôpital Privé Jean Mermoz
Lyon, France Recruiting
Study contacts
- Study coordinator: Jean-François Oudet
- Email: jf.oudet@ecten.eu
- Phone: 0033683346567
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.