Active Release Technique Verses Proprioceptive Neuromuscular Facilitation on Hamstring Flexibility in Patients Having Specific Low Back Pain
Comparative Effects of Active Release Technique Verses Proprioceptive Neuromuscular Facilitation on Hamstring Flexibility in Patients Having Specific Low Back Pain
1 other identifier
interventional
40
1 country
1
Brief Summary
The goal of this clinical trial is to learn whether Active Release Technique (ART) or Proprioceptive Neuromuscular Facilitation (PNF) is more effective in improving hamstring flexibility in adults with specific low back pain. It will also look at how these treatments affect pain and movement. The main questions it aims to answer are: Does ART or PNF improve hamstring flexibility more in people with specific low back pain? Do participants report reduced pain and better movement after receiving either treatment? Researchers will compare the effects of ART and PNF to see which method works better for improving flexibility and reducing pain. Participants will: Receive either ART or PNF therapy for 2 weeks Attend regular physiotherapy sessions during the treatment period Be assessed before and after treatment for hamstring flexibility and pain levels
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable low-back-pain
Started Nov 2025
Shorter than P25 for not_applicable low-back-pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 5, 2025
CompletedFirst Posted
Study publicly available on registry
August 12, 2025
CompletedStudy Start
First participant enrolled
November 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 25, 2025
CompletedJanuary 27, 2026
May 1, 2025
1 month
August 5, 2025
January 26, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Hamstring Flexibility (measured by Passive Straight Leg Raise Test)
Flexibility of the hamstring muscle will be measured using a goniometer during the Passive Straight Leg Raise (SLR) test.
at baseline then at 2nd and at 4th week after the last Session
Secondary Outcomes (1)
Pain Intensity (measured by Numeric Pain Rating Scale - NPRS)
at baseline then at 2nd and at 4th week after the last Session
Study Arms (2)
active release technique
EXPERIMENTALThis group receives Active Release Technique applied on the hamstring muscle group to improve flexibility in patients with specific low back pain. Sessions are given at baseline then at 2nd and at 4th week after the last Session
Proprioceptive Neuromuscular Facilitation
ACTIVE COMPARATORThis group receives PNF stretching for the hamstring to enhance flexibility in patients with specific low back pain. Sessions are given at baseline then at 2nd and at 4th week after the last Session
Interventions
A manual therapy technique applied to release soft tissue tension in the hamstrings.
A stretching technique involving passive stretching and isometric contractions of the hamstrings.
Eligibility Criteria
You may qualify if:
- Patients having chronic low backache having hamstring tightness referred from orthopedic department
- Patients having lumber disc budge, spinal spondylosis
- Age group 25-40 years, having pain more than 3 months
- Minimum 20-degree restriction in SLR unilaterally Both male and female
You may not qualify if:
- Any history of injury in lower extremities in past 3 months
- Knee osteoarthritis patients, knee deformities, discitis, osteomyelitis
- Patients with injury of back, constant or severe persistent pain, inflammatory conditions (rheumatoid arthritis, ankylosing spondylitis, spinal infection lumber spondylolisthesis, and lumber spondylolysis.
- Any pregnancy, history of previous surgery or fracture and history of radiculopathy or neuropathic pain.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Lahore Poly Clinic, social security hospital
Lahore, Punjab Province, 54000, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Montiha Azeem, DPT
University of Lahore
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- The participants were randomly assigned in to two groups i.e. Group A and Group B by sealed envelope method.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 5, 2025
First Posted
August 12, 2025
Study Start
November 20, 2025
Primary Completion
December 20, 2025
Study Completion
December 25, 2025
Last Updated
January 27, 2026
Record last verified: 2025-05