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Fascial-muscular Lengthening Therapy in the Patients With Chronic Low Back Pain.

CompletedNot applicableNCT04760366
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The purpose of this study is to assess and evaluate tight iliopsoas muscle in patients with chronic low back pain and to increase hip flexor flexibility in the patients with chronic low back pain by using the technique of manual fascial-muscular lengthening therapy .

Study details

Official title
Effects of Fascial-muscular Lengthening Therapy on Tight Iliopsoas Muscle in the Patients With Chronic Low Back Pain.
Interventions
  • Other: fascial- muscular lengthening therapy
  • Other: Stretching's of iliopsoas muscle
  • Other: the conventional therapy
Sponsor
Riphah International University
Start date
2020-08-13
Primary completion
2021-03-20
Sex
Female
Age range
from 25 Years to 45 Years
Results posted
No results posted in this snapshot
Countries
Pakistan
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * • The study includes female patients with chronic low back pain. * The study includes patients from the age group of 25 years and 45. * The study includes patients with low back pain for more than 3 months. * The study includes patients with chronic bilateral tight hip flexors which will assessed through Thomas Test * Pain in flexion bias Exclusion Criteria: * • The study excludes male patients. * No history of serious underlying pathology, nerve root compromise, structural deformities, genetic spinal disorders or previous spinal surgery

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04760366