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Clinical Trials/IRCT20230411057885N1
IRCT20230411057885N1
Not yet recruiting
未知

Comparison of the effect of performing therapeutic selected exercises using virtual reality and routine method on pain, function and quality of life in patients with non-specific chronic low back pain.

niversity of social welfare and rehabilitation sciences0 sites44 target enrollmentTBD
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Conditionspatients suffering chronic non specific low back pain.Dorsalgia, unspecifiedM54.9

Overview

Phase
未知
Intervention
Not specified
Conditions
patients suffering chronic non specific low back pain.
Sponsor
niversity of social welfare and rehabilitation sciences
Enrollment
44
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of social welfare and rehabilitation sciences

Eligibility Criteria

Inclusion Criteria

  • •People with non\-specific chronic mechanical back pain with the diagnosis of the attending physician and file.
  • •People who are between 20\-50 years old.
  • •They are not involved in any other treatment program during the study.
  • •Have stopped taking painkillers 24 hours before the evaluation.
  • •Having a history of back pain for at least 12 weeks.
  • •Have an average pain of 4\-7 on the visual analog scale of pain in the previous seven days.

Exclusion Criteria

  • •Patients with congenital abnormalities.
  • •History of trauma
  • •Fracture of the spine or lower and upper limbs
  • •Any systemic disease or neurological disease
  • •Individuals who have taken corticosteroids, benzodiazepines, antidepressants, or anticonvulsants three weeks prior to the evaluation.
  • •pregnant women
  • •previous back surgeries
  • •Vestibular and vision disorders
  • •Obese people according to body mass index
  • •Aggravation of symptoms so that it is not possible to perform.

Outcomes

Primary Outcomes

Not specified

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