RecruitingNCT05108948

Research of Factors Determining the Improvement of Quality of Life at One Year of Adult Patients Treated for Spinal Deformity (COFTASD)

Research of Factors Determining the Improvement of Quality of Life at One Year of Adult Patients Treated for Spinal Deformity : Observational Study (COFTASD)


Sponsor

Elsan

Enrollment

866 participants

Start Date

Oct 23, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

The objective of this study is to find the predictive factors of improvement of the quality of life of operated patients from spinal deformity.


Eligibility

Min Age: 18 Years

Inclusion Criteria9

  • Age over 18 years-old
  • Diagnosis of Adult Spinal Deformity with any of the deformity characteristics following:
  • Scoliosis with a Cobb angle ≥ 20 °
  • Vertical sagittal axis (SVA) ≥ 5 cm
  • Pelvic tilt ≥25 °,
  • Thoracic kyphosis with a Cobb angle ≥ 60 °
  • Eligible for surgery
  • Having given their participation agreement
  • Affiliate or beneficiary of a social security scheme

Exclusion Criteria6

  • Age under 18 years-old
  • Patient unlikely to comply with follow-up
  • Patient with long-term complete paraplegia
  • Patient unable to understand and answer questionnaires in due to language difficulties or cognitive impairment
  • Pregnant or breastfeeding woman
  • Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALQuality of life questionnaires

Oswestry Disability Index Scoliosis Research Society-22R Short Form 36 Health Survey Questionnaire Tobacco, Alcohol, Prescription medication, and other Substance use Core Outcome Measures Index : back and neck

PROCEDURERadiography

Spinal radiography : full, face, profile


Locations(1)

Clinique du dos

Bruges, France

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05108948


Related Trials