RecruitingNot ApplicableNCT07749534

Quality of Life, Psychosocial Burden, and Structural-functional Status in Adults With Spinal Deformity.


Sponsor

Universitaire Ziekenhuizen KU Leuven

Enrollment

320 participants

Start Date

Aug 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Reoperation and a procedure called first corrective surgery for people with asd, scoliosis idiopathic adolescent, and other related conditions. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREfirst corrective surgery

patients undergoing a first corrective surgery or reoperation for ASD

PROCEDUREReoperation

patients undergoing a reoperation


Locations(1)

UZ Leuven

Leuven, Belgium

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NCT07749534


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