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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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07118787
Enrollment
40
Registered
2025-08-12
Start date
2025-11-20
Completion date
2025-12-25
Last updated
2026-01-27

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

Conditions

Low Back Pain

Keywords

active release technique, low back pain, muscle stretching

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

Detailed description

This randomized controlled trial was designed to compare the effectiveness of Active Release Technique (ART) and Proprioceptive Neuromuscular Facilitation (PNF) in improving hamstring flexibility among individuals with specific low back pain. Reduced hamstring flexibility is a common contributing factor in low back dysfunction, and identifying the most effective manual therapy technique can guide more targeted physical therapy interventions. Participants were randomly assigned to receive either ART or PNF over a 2-week intervention period. Both groups received treatment administered by trained physiotherapists using standardized protocols. ART focused on applying specific manual pressure to soft tissues while moving the muscle through its range of motion, while PNF employed contract-relax stretching techniques to promote muscle lengthening and neuromuscular facilitation. Participants were evaluated at baseline and after the completion of the intervention for changes in hamstring flexibility, with secondary observations on pain reduction and functional improvement. The study adhered to ethical standards, and all participants provided informed consent prior to participation. The trial contributes to evidence-based physiotherapy by offering comparative insight into two widely used manual techniques in musculoskeletal rehabilitation.

Interventions

OTHERProprioceptive Neuromuscular Facilitation

A stretching technique involving passive stretching and isometric contractions of the hamstrings.

OTHERActive Release Technique

A manual therapy technique applied to release soft tissue tension in the hamstrings.

Sponsors

University of Lahore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

The participants were randomly assigned in to two groups i.e. Group A and Group B by sealed envelope method.

Intervention model description

After screening the population based on inclusion and exclusion criteria, participants were included in the study. Participants signed a consent form regarding their willingness to participate in the study. The participants were divided equally into two groups where group one was evaluated for active release technique and group two was evaluated according to proprioceptive neuromuscular facilitation technique. The measurements were taken at baseline then at 2nd and at 4th week after the last Session. There were total 20 sessions, 5 sessions in a week for 4 weeks

Eligibility

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

Inclusion criteria

1. Patients having chronic low backache having hamstring tightness referred from orthopedic department 2. Patients having lumber disc budge, spinal spondylosis 3. Age group 25-40 years, having pain more than 3 months 4. Minimum 20-degree restriction in SLR unilaterally Both male and female

Exclusion criteria

1. Any history of injury in lower extremities in past 3 months 2. Knee osteoarthritis patients, knee deformities, discitis, osteomyelitis 3. Patients with injury of back, constant or severe persistent pain, inflammatory conditions (rheumatoid arthritis, ankylosing spondylitis, spinal infection lumber spondylolisthesis, and lumber spondylolysis. 4. Any pregnancy, history of previous surgery or fracture and history of radiculopathy or neuropathic pain. \-

Design outcomes

Primary

MeasureTime frameDescription
Hamstring Flexibility (measured by Passive Straight Leg Raise Test)at baseline then at 2nd and at 4th week after the last SessionFlexibility of the hamstring muscle will be measured using a goniometer during the Passive Straight Leg Raise (SLR) test.

Secondary

MeasureTime frameDescription
Pain Intensity (measured by Numeric Pain Rating Scale - NPRS)at baseline then at 2nd and at 4th week after the last SessionParticipants will rate their pain intensity on a scale from 0 (no pain) to 10 (worst pain imaginable).

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORMontiha Azeem, DPT

University of Lahore

Outcome results

None listed

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