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Clinical Trials/CTRI/2021/03/031733
CTRI/2021/03/031733Not ApplicableNot Applicable

Clinical outcomes and psychosocial effectiveness of Yoga therapy versus Pilate’s exercises in school teachers with non-specific chronic low back pain – A randomized controlled trial.

Primary Sponsor Prince Sattam Bin Abdulaziz University Al Kharj Saudi Arabia1 site in 1 country76 target enrollmentStarted: October 3, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not Applicable
Sponsor
Enrollment
76
Locations
1
Primary Endpoint
Visual analog scale

Study Overview

Brief Summary

Yoga and exercise interventions are usually delivered in physicaltherapy clinics for treating chronic low back pain condition. It includes different postures appliedfor the joints and other structures, Yoga therapy and other different forms of exercisesare delivered by various clinicians, including yoga specialists, physiotherapists,physical therapists, chiropractors and osteopaths. The aims of both types ofinterventions are to relieve pain, promote healing, reduce muscle spasms,increase joint range, strengthen weakened muscles and improve biomechanics andfunction. Hence this study is trying to find its different effects in school teachers with chroniclow back pain.

Study Design

Study Type
Interventional
Allocation
Permuted block randomization, fixed
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
30.00 Year(s) to 60.00 Year(s) (—)
Sex
Male

Inclusion Criteria

  • •Male school teachers in the age group of 30 to 60 years, chronic ( more than 3 months) LBP and 4 to 8 pain intensity in visual analog scale (VAS) will be included.

Exclusion Criteria

  • •Participants with severe musculoskeletal, neural, somatic, and psychiatric conditions, waiting for spine surgery, having alcohol or drug abuse, involving in other weight and balance training program will be excluded from the study.
  • •Participants with other soft tissue injuries, fracture at the lower limbs and pelvic bone, deformities will also be excluded from the study.

Outcomes

Primary Outcomes

Visual analog scale

Time Frame: Outcomes measured at baseline, after 4 weeks, 8 weeks and at 6 months.

Secondary Outcomes

  • Range of motion(Functional disability)

Investigators

Sponsor
Primary Sponsor Prince Sattam Bin Abdulaziz University Al Kharj Saudi Arabia
Sponsor Class
Government funding agency

Study Sites (1)

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