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Clinical Trials/CTRI/2022/03/041143
CTRI/2022/03/041143
Active, not recruiting
未知

Effect of exercise interventions in improving clinical outcomes in a sub-group of population with chronic low back pain positive for central sensitization

Integral University0 sites215 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: M999- Biomechanical lesion, unspecified
Sponsor
Integral University
Enrollment
215
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Integral University

Eligibility Criteria

Inclusion Criteria

  • 1\.Persons between 18\-59 years of age
  • 2\.CLBP of more than 3 months duration
  • 3\.Pain intensity of more than 4
  • 4\.Positive for Central Sensitization\-related sign and symptoms \[Smart et al., 2011]
  • 5\.Cognitively intact \[Mini\-Mental State Examination score \>24]
  • 6\.Basic working knowledge of English language
  • 7\.Should not be suffering from any other chronic pain condition, high blood pressure, Raynaud’s disease, frostbite, any open cut, sore, or bone fracture, other major illness such as cancer, visual and/or hearing impairment, and psychiatric disorders.
  • 8\.Further, all participants will be screened for contraindications to exercise using the Physical Activity Readiness Questionnaire and any participant who provides positive response to items 1, 2, 3, 4, 6 or 7 will be referred to a physician for medical clearance \[ACSM, 1995].

Exclusion Criteria

  • 1\.Participants who are contra\-indicated to participate in physical activity \[Medicine, 2010]
  • 2\.Participants who have undertaken any surgical procedures to spine or suffering from symptomatic spine diseases.
  • 3\.Participants, who report acute pain within 48 hours prior to the appointment
  • 4\.Participants, who have taken any analgesic, hypnotic or antidepressant medication in the past 72 hours.

Outcomes

Primary Outcomes

Not specified

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