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Assessing the Quality of Life in Adults With Spinal Deformity

I

Istituto Scientifico Italiano Colonna Vertebrale

Status

Completed

Conditions

Quality of Life
Scoliosis

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT05333757
A-ISYQOL

Details and patient eligibility

About

Spinal deformities, such as scoliosis, can have a significant impact on the physical and psychological health of patients. Over time, specific tools for this condition have been developed to investigate the extent of this impact, such as the SRS-22 questionnaire and ISYQOL questionnaire.

The latter was initially used for underage patients, but given that some of them continue their therapy and the monitoring beyond the age of 18, we have continued its use in these subjects as well. Given the clinical usefulness and given the lack of questionnaires developed in the Rasch environment for adults, we have extended the application of the ISYQOL questionnaire to the adult population. However, a comparison between the ISYQOL and SRS-22 in adults has not yet been made.

The objective of this study is to verify the validity of ISYQOL and to compare the properties of ISYQOL with those of the SRS-22 questionnaire in adults with spinal deformity.

Enrollment

150 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 years
  • Diagnosis of idiopathic or degenerative scoliosis with ≥30 ° Cobb curve

Exclusion criteria

  • Previous spinal surgery
  • Previous and relevant illnesses, surgery or trauma

Trial design

150 participants in 1 patient group

Quality of life
Description:
Adult patients treated conservatively for idiopathic scoliosis or undergoing clinical monitoring who have completed both questionnaires at least once and simultaneously and who meet the following inclusion criteria: * Age ≥ 18 years * Diagnosis of idiopathic or degenerative scoliosis with curve ≥30 ° Cobb
Treatment:
Other: Questionnaire

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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