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Scoliosis and Quality of Life of Adolescents (SQUAD)

T

Toulouse University Hospital

Status

Completed

Conditions

Scoliosis

Treatments

Other: First time measure
Other: Second time measure
Other: Third time measure

Study type

Observational

Funder types

Other

Identifiers

NCT02890654
RC31-15-7475

Details and patient eligibility

About

Around the scoliosis surgery, the pain (pre or post operative, physical, psychological, fantasy or real) is a major concern for adolescents and their families. She is also a key concern of caregivers, both its assessment and management is complex. this pain involved predominantly in the quality of life of these teenagers today who will become the adults of tomorrow.

To date in France, no study aims to describe and evaluate the effect of a multidisciplinary approach and its impact on the quality of life of these young people made.

The present study wish to prevent, anticipate and limit the short, medium and long-term morbidity. Focus will be on pain and its management, on preparing for surgery, hospitalization, follow-up after surgery, rehabilitation until recovery.

Help teens reclaim their bodies after the changes caused by the intervention is a major issue.

This study believe that support good quality, adapted to patient needs will limit operating and postoperative pain in the medium and long term.

Medical team developed special attention around the teenagers that are operated for scoliosis (teen groups and parent groups, interview before the operation and counseling, physiotherapy support ...).

The present study would systematize data collections in order to have a comprehensive and accurate assessment of the care.

The qualitative research will focus on the multidisciplinary care in an effort to evaluate the whole course of these teenagers, their experience and to identify efforts to put in place to optimize the current care.

Enrollment

95 patients

Sex

All

Ages

12 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients followed for idiopathic scoliosis with indication for surgery
  • Patients monitored and operated at the Children Hospital of Toulouse

Exclusion criteria

  • Opposition to the participation
  • Spine deformations other than scoliosis
  • Non idiopathic scoliosis

Trial design

95 participants in 1 patient group

Teenagers with scoliosis
Description:
Patients will be evaluated at three times during the study : * First time measure : 1 month before the scoliosis surgery * Second time measure : 3 months after the scoliosis surgery * Third time measure : 1 year after the scoliosis surgery
Treatment:
Other: First time measure
Other: Second time measure
Other: Third time measure

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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