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Pain, Physical Activity, Posture and Quality of Life in Post-COVID-19 Individuals With Idiopathic Scoliosis

I

Izmir Democracy University

Status

Completed

Conditions

COVID-19 Respiratory Infection
Idiopathic Scoliosis

Treatments

Other: Physical Evaluations of post-COVID-19 individuals
Other: Physical evaluations of non-post-COVID-19 individuals

Study type

Observational

Funder types

Other

Identifiers

NCT06006897
Effects of COVID on scoliosis

Details and patient eligibility

About

It is not known to what extent the COVID-19 virus affects individuals with scoliosis during the prolonged COVID-19 pandemic. Therefore, in this study it was aimed to comparatively investigate pain severity, posture disorders that can be assessed by artificial intelligence, physical activity levels and quality of life in individuals with idiopathic scoliosis with and without COVID-19.

Full description

Various physical and psychological disorders observed in individuals with scoliosis have worsened during the pandemic period. However, it is still not fully known to what extent the COVID-19 virus affects individuals with scoliosis during the prolonged COVID-19 pandemic. For this reason, this study aimed to comparatively investigate pain severity, posture disorders that can be assessed by artificial intelligence, physical activity levels and quality of life in individuals with idiopathic scoliosis with and without COVID-19.

With the findings obtained from this way, it is expect that artificial intelligence technology will shed light on a new approach to the rehabilitation of individuals with idiopathic scoliosis who have suffered from COVID-19. In addition, if there is more pain, posture disorders, physical inactivity and quality of life disorders in individuals with scoliosis who have previously experienced COVID-19, it is also aimed to bring them to light. In this way, it will be possible to provide more specific direction to the rehabilitation of these individuals.

Enrollment

41 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for individuals with idiopathic scoliosis who have experienced COVID-19:

  • being 18 years of age or older
  • Volunteering to participate in the study
  • Having been diagnosed with idiopathic scoliosis
  • Being able to walk independently
  • Having been diagnosed with COVID-19 and having recovered and been discharged.

Inclusion criteria for individuals with idiopathic scoliosis who have not had COVID-19;

  • being 18 years of age or older
  • Volunteering to participate in the study
  • Being diagnosed with idiopathic scoliosis

Exclusion criteria for individuals with idiopathic scoliosis who have had COVID-19;

  • Having been diagnosed with COVID-19 in the last 15 days
  • Being suspected of COVID-19
  • Having mental problems that may affect cooperation
  • Having an acute or chronic infection that may affect the evaluations to be made within the scope of the study.
  • Participating in any professional sports activity
  • Having any surgery to prevent walking, having a chronic disease, orthopedic/neurological/cardiopulmonary disease, physical or mental disability and/or cognitive impairment
  • Using analgesics and other interactive drugs that will affect assessments
  • Being pregnant

Exclusion criteria for individuals with idiopathic scoliosis who have not had COVID-19;

  • Having had at least one COVID-19
  • Being suspected of COVID-19
  • Having any mental or physical disability
  • Having any acute or chronic illness
  • Having analgesic drug use that will affect the evaluations . Being pregnant

Trial design

41 participants in 2 patient groups

Post-COVID-19 group
Description:
This group will consist of individuals with idiopathic scoliosis who have had COVID-19.
Treatment:
Other: Physical Evaluations of post-COVID-19 individuals
Control group
Description:
The control group will consist of individuals with idiopathic scoliosis without post-COVID-19.
Treatment:
Other: Physical evaluations of non-post-COVID-19 individuals

Trial contacts and locations

1

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Central trial contact

GÜLŞAH BARĞI; MERVE NUR YÜKSEL

Data sourced from clinicaltrials.gov

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