This study examines which factors influence quality of life in adults with a spinal deformity. It looks at imaging findings together with pain, daily functioning, psychosocial factors, and frailty to support more person-centred care. A total of 320 adults will participate in three groups: conservative treatment, first corrective surgery, or reoperation. All care follows standard practice; no experimental treatments are added. Participants complete questionnaires, and routine FASD tests and existing EOS/X-ray images may be used. Follow-up lasts up to 2 years, with scheduled assessments depending on whether treatment is surgical or conservative.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Cross-sectional associations in QoL between conservative, primary surgery, and revision surgery study groups.
Timeframe: within a period of 2 year
Cross sectional associations in QoL between conservative, primary surgery, and revision surgery study groups.
Timeframe: Withing 2 years
Cross sectional associations in QoL between conservative, primary surgery, and revision surgery study groups.
Timeframe: Withing 2 years
Cross sectional associations in QoL between conservative, primary surgery, and revision surgery study groups.
Timeframe: Withing 2 years
Cross-sectional associations in psychosocial burden between conservative, primary surgery, and revision surgery study groups.
Timeframe: within a period of 2 year
Cross sectional associations in psychosocial burden between conservative, primary surgery, and revision surgery study groups.
Timeframe: Withing 2 years
Cross sectional associations in psychosocial burden between conservative, primary surgery, and revision surgery study groups.
Timeframe: Withing 2 years
Cross sectional associations in psychosocial burden between conservative, primary surgery, and revision surgery study groups.
Timeframe: Withing 2 years
Cross-sectional associations in functional impairment between conservative, primary surgery, and revision surgery study groups.
Timeframe: within a period of 2 year
Cross sectional associations in functional impairment between conservative, primary surgery, and revision surgery study groups.
Timeframe: Withing 2 years