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NCT05347368

Effects of Primal Reflex Release Technique in Chronic Non-specific Low Back Pain

Status unknown NA Last updated 16 June 2022
What this trial tests

NA trial testing Control group (conventional therapy) in Chronic Non-specific Low Back Pain in 28 participants. Status unknown.

Timeline
25 April 2022
Primary endpoint
25 December 2022
10 January 2023

Quick facts

Lead sponsorRiphah International University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment28
Start date25 April 2022
Primary completion25 December 2022
Estimated completion10 January 2023
Sites1 location across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

Riphah International University

Who can join

Adults 25 to 45, any sex, with Chronic Non-specific Low Back Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Low back pain is a major disorder which occurs from chronic over use and injury to lumbar musculoskeletal system. Sometimes the source of pain is non-specific leading to pain and spasm due to muscle imbalance. Primal reflex release technique is a novel concept to decrease pain and muscle spasm by resetting reflexes using reciprocal inhibition following the concept of rebooting the Autonomic nervous system. This study aims to determine the effects of primal reflex release technique on pain, flexibility and disability in chronic nonspecific low back pain patients. This study will be a Randomized Controlled trial and will be conducted at Arif Memorial Hospital in Lahore. A sample size of Total 32 patients will be taken in this study using consecutive sampling technique. Patients will be randomly assigned into two groups. Group A will be treated by conventional therapy and Group B will be treated by conventional therapy and primal reflex release technique. Numeric Pain Rating Scale and Ronald Morris Disability Questionnaire will be used to evaluate pain and disability respectively. Flexibility of low back, Iliopsoas, hamstring, Piriformis and gastrocnemius will be measured by schober's test, modified Thomas test, Active knee extension test, FAIR test and active dorsiflexion, respectively. The evaluation will be on day 1 as pretreatment values and at 2nd and 4th week as post treatment values respectively. The collected data will be analyzed on SPSS - 25.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Chronic Non-specific Low Back Pain

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