PRT Versus CBT on Chronic Non Specific LBP

Positional Release Technique Versus Cognitive Behavioral Therapy on Chronic Non Specific Low Back Pain

Status

Recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06198660

Enrollment

Registered

2024-01-10

Start date

2023-09-15

Completion date

2024-12-31

Last updated

2024-01-12

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

Conditions

Chronic Non Specific Mechanical Low Back Pain

Keywords

positional release, cognitive behavioral therapy

Brief summary

The goal of this clinical trial is to compare between the effect of positional release technique and cognitive behavioral therapy in patients with chronic non specific low back pain. The main question aims to answer :Is there any differences of using positional release techniques versus cognitive behavioral therapy on patients with chronic low back pain?

Detailed description

Design of the study : Pretest-posttest randomized controlled trial. Subjects selection : sixty patients their age between 25-45 years of both genders with chronic non specific low back pain will participate in this study according tosample size calculation.

Interventions

OTHERpositional release technique

positional release techniques in addition to conventional therapy two sessions per week for 6 weeks

OTHERcognitive behavioral therapy

cognitive behavioral therapy in addition to conventional therapy two sessions per week for 6 weeks

OTHERconventional therapy only

conventional therapy two sessions for 6 weeks

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE (Subject, Outcomes Assessor)

Masking description

double

Eligibility

Sex/Gender

ALL

Age

20 Years to 40 Years

Healthy volunteers

Inclusion criteria

* All patients will be clinically diagnosed with chronic non specific low back pain . * Their ages will range from 20to40years old. * body mass index will range from 18 to 30 kg/cm². * Cognitive score will be 23 or above . * Voluntary acceptance of participation in this study.

Exclusion criteria

* Lumbar canal stenosis * Lumbar discogenic lesions * Lumbar infections,tumors.arthiritis * Patients with decreased range of motion due to congenital anamolies. * Cognitive and emotional disturbances

Design outcomes

Primary

Measure	Time frame	Description
pressure algometer	pre intervention and immediately after intervention	change in pain pressure threshold .with unit of measurement kg/cm2

Secondary

Measure	Time frame	Description
the arabic version of oswestry disability questionnaire	pre intervention and immediately after intervention	the patients choose one out of six senteces 10 multiple choise questions for back pain higher scores indicate great pain

Countries

Egypt

Contacts

Primary ContactNosaiba Eissa

neissa@horus.edu.eg01005305615

Outcome results

None listed

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