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Comparison of Positional Release and Manual Pressure Technique in Chronic Low Back Pain

Comparative Effects of Positional Release and Manual Pressure Techniques of Tight Hip Flexors on Pain, Range of Motion, Lumbosacral Angle, and Disability in Patients With Chronic Low Back Pain

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06240949
Enrollment
46
Registered
2024-02-05
Start date
2023-11-05
Completion date
2024-02-05
Last updated
2024-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Low-back Pain

Keywords

Low back pain, Chronic low back pain, Hip flexors, positional release technique, Manual Pressure Technique

Brief summary

The purpose of the study is to compare the effect of positional release technique and manual pressure technique of hip flexors on pain, range of motion, lumbosacral angle and disability in patients with chronic low back pain

Detailed description

This will be Randomized clinical trial. Individuals who met inclusion criteria will be included in this study. All participants will go through randomization and divided into two groups. Pre intervention assessment is made for both groups. Then intervention will apply to both groups. Group A will receive positional release technique and Group B will be treated by manual pressure technique and pain, range of motion, lumbosacral angle and functional disability will be measured before and after the treatment using NPRS, Inclinometer and ODI. Estimated time of treatment protocol will be 30 minutes per session, 4 times/week for 4 weeks in the hospital setting. Subjects will be evaluated at baseline and 4th week assessment will be the final.

Interventions

Positional Release Technique will be applied on iliopsoas muscle. Treatment time will be 30 minutes per session, 4 times/week for 4 weeks in the hospital setting.

Manual Pressure Technique will be applied on iliopsoas muscle. Treatment time will be 30 minutes per session, 4 times/week for 4 weeks in the hospital setting.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Males and females * age group 25 to 40yrs * Atraumatic chronic low back pain more than 3 months * Patients with Anterior pelvic tilt * Patients with lumbosacral angle \> than 50 degrees

Exclusion criteria

* Pregnancy * history of vertebral fracture * History of any spinal surgery * Disc disease * Osteoporosis * Bone disease * Patient unable to give consent

Design outcomes

Primary

MeasureTime frameDescription
Hip flexors tightness4th weekHip flexors tightness will be assessed using an inclinometer to measure the range of motion (ROM) for active hip extension and Lumbosacral angle
Pain Intensity4th weekPain intensity will be evaluated using the Numeric Pain Rating Scale (NPRS)
Functional disability4th weekFunctional disability will be assessed by Oswestry disability questionnaire.
Anterior pelvic tilt4th weekAnterior pelvic tilt will be measured using an inclinometer

Countries

Pakistan

Contacts

Primary ContactImran Amjad, phD
imran.amjad@riphah.edu.pk03324390125

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026