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Active Not RecruitingNCT06548334

The Effectiveness of Lumber Regression Technique on Disc Bulge Randomized Control Trial

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
22 (actual)
Sponsor
Superior University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Lumbar disc bulges lead to considerable pain and disability in affected individuals, with current interventions lacking consistency of outcomes. The lumbar regression method offered a hopeful, noninvasive option.

Detailed description

this study was proposed to evaluate its efficacy in improving accessary lower limb flexibility and reducing functional disability and pain management. To provide evidence about its effectiveness and help with clinical practice, this study aimed to improve patient outcomes in subjects having lumbar disc bulges.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTAdvanced PhysiotherapyThe physiotherapist used the regression techniques for 1 hour of session 2 times for 8 weeks. The caudal component involved the spinous process of the treated segment touching the therapist's hand and not applying force as though mobilising the segment at grade 2. These were applied if there is a suspected case of a posterolateral disc prolapse where the aim is to increase the diameter of the foramen and decrease the tension exerted on the nerve root. Applied posteroanterior was used to distract the anterior intervertebral end plate and to approximate the posterior end plates so as to pull back the protruded nuclear material by creating a negative pressure.
OTHERConventional Physiotherapy TechniquesIn traditional physiotherapy, the patient underwent two sessions per week for eight weeks. Each session lasted one hour and included 20minutes of TENS treatment. The flexibility exercises consisted of hamstring stretches and single and double knee-to-chest stretches. The strengthening exercises were partial sit-ups, quadruped lifts, and double leg hold; pelvic tilts were performed with 10-15 repetitions, each held for 20-30 seconds and repeated three times.

Timeline

Start date
2023-10-01
Primary completion
2024-04-01
Completion
2024-09-30
First posted
2024-08-12
Last updated
2024-08-12

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06548334. Inclusion in this directory is not an endorsement.