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Low Back PainNCT07426562

Post Facilitatiion Stretch and Dry Needling on Hamstring Tightness in Chronic Low Back Pain

A study testing Dry Needling along with Conventional Therapy and Post Facilitation Stretch along with Conventional Therapy in people with Low Back Pain, run by Riphah International University at 1 site in Pakistan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The aim of this research is to compare the effects of post-facilitation stretch and dry needling on hamstring flexibility, pain, lumbar range of motion, pelvic tilt, and functional status in patients with chronic low back pain. Read more about this study

Who is it for?
Ages 20 to 50 years
Conditions the study is for
Low Back Pain
What is being tested?
Dry Needling along with Conventional Therapy and Post Facilitation Stretch along with Conventional Therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
36 participants
Where
1 sitePakistan
Study dates
2 Feb 2026to 31 Aug 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Diagnosed with chronic non-specific low back pain of more than 12 weeks' duration.
  • Positive Straight Leg Raise (SLR) test or Active Knee Extension Test showing hamstring tightness (<80° hip flexion with knee extended).

Who cannot join

  • History of spinal surgery, fracture, or neurological deficit.
  • Radiculopathy or red flag signs (tumor, infection, inflammatory disorders).
  • Recent steroid injection therapy for low back pain (within 3 months).
  • Contraindications to dry needling (bleeding disorders, infection at site, needle phobia).
  • Pregnancy.
  • Severe needle phobia (for DN group).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Imran Amjad PT, PhD contact

03324390125

imran.amjad@riphah.edu.pk

Pakistan1 site, 1 recruiting
  • Spine Physical Therapy and Rehabilitation Center

    Peshawar, Khyber Pakhtunkhwa, 25000

    Aiman Basheer, DPT, +92 318 945 8557, aimanbasheer444@gmail.com

    Recruiting

Other trials in Pakistan

About this study

Official title: Comparison of Post Facilitatiion Stretch and Dry Needling on Hamstring Tightness in Chronic Low Back Pain

The aim of this research is to compare the effects of post-facilitation stretch and dry needling on hamstring flexibility, pain, lumbar range of motion, pelvic tilt, and functional status in patients with chronic low back pain. This randomized clinical trial will be conducted at Spine Care Physical Therapy and Rehabilitation Centre (SPRC), Peshawar. The sample size will be 36 participants, who will be randomly divided into two groups: 18 participants in the post-facilitation stretch group and 18 participants in the dry needling group. The study duration will be 3 weeks, with interventions applied three times per week. The sampling technique used will be non-probability purposive sampling, followed by random allocation using the sealed opaque envelope method. Participants aged 20-50 years diagnosed with chronic nonspecific low back pain and having hamstring tightness will be included. Outcome measures used in the study will be Active Knee Extension Test (goniometer) for hamstring flexibility, Numeric Pain Rating Scale (NPRS) for pain, goniometer for lumbar flexion and extension, pelvic inclinometer for pelvic tilt, and Modified Oswestry Disability Index (MODI) for functional disability.

Read the detailed description

Chronic low back pain (CLBP), defined as pain persisting for more than 12 weeks, represents one of the leading causes of long-term disability worldwide. In the absence of a clearly identifiable structural pathology, the majority of cases are classified as chronic non-specific low back pain, which poses significant challenges for accurate diagnosis and targeted management. The Global Burden of Disease (2023) report highlights low back pain as the highest-ranking musculoskeletal condition in terms of disability, affecting approximately 7.5% of the global population, with lifetime prevalence estimates reaching up to 80% and projected to rise further by 2050.Chronic low back pain is closely associated with musculoskeletal dysfunctions, including impaired trunk muscle control, altered pelvic mechanics, and compensatory movement strategies involving the hip and lower extremities. Disruption of normal movement patterns and muscle imbalances contributes to abnormal load distribution across the lumbar spine, thereby perpetuating pain and functional limitation. In particular, restricted pelvic mobility during trunk flexion and extension results in excessive lumbar spine motion, increasing mechanical stress on spinal structures.Lifestyle and behavioral factors play an important role in the development and progression of CLBP. Emerging evidence suggests that regular moderate physical activity has a protective effect against chronicity. A recent prospective cohort study (2025) demonstrated that individuals engaging in more than 100 minutes of daily walking exhibited a significantly lower risk of developing chronic low back pain. In contrast, psychosocial factors such as depression have been shown to negatively influence pain severity, disability levels, and recovery outcomes, emphasizing the multifactorial nature of CLBP.

Hamstring muscle tightness is a commonly observed impairment in individuals with CLBP and has been identified as a key contributor to altered lumbopelvic rhythm. The hamstring muscle group comprising the semitendinosus, semimembranosus, and long head of the biceps femoris originates from the ischial tuberosity and plays a crucial role in regulating hip and knee mechanics. Reduced hamstring flexibility limits anterior pelvic tilt during forward bending, leading to compensatory lumbar spine motion and increased repetitive loading. Chronic hamstring tightness is frequently accompanied by weakness of the gluteus maximus and deep core stabilizers, resulting in posterior chain imbalance and reliance on superficial stabilizers such as the erector spinae, further aggravating pain persistence.Improving hamstring flexibility is therefore considered an important therapeutic target in the management of chronic non-specific low back pain. Various stretching techniques, including static stretching, have demonstrated effectiveness in increasing range of motion and reducing musculotendinous stiffness. Improved flexibility has been associated with favorable changes in muscle activation patterns and a more balanced distribution of movement between the pelvis and lumbar spine, potentially reducing mechanical strain.

Among manual therapy interventions, Dry Needling (DN) has gained increasing attention as an invasive technique designed to deactivate myofascial trigger points, normalize muscle tone, and reduce nociceptive input. DN has shown effectiveness in reducing pain sensitivity, relieving muscle tightness, and improving functional movement, particularly when combined with exercise-based rehabilitation. Evidence from systematic reviews and meta-analyses supports its short- to mid-term benefits in reducing pain and disability in individuals with CLBP.Similarly, Muscle Energy Technique (MET), particularly in the form of post-facilitation stretch (PFS), has demonstrated strong efficacy in improving hamstring flexibility. PFS utilizes a maximal voluntary contraction followed by an immediate stretch to enhance muscle extensibility through neuromuscular mechanisms such as post-isometric relaxation and reciprocal inhibition. Compared to conventional stretching, MET has been shown to produce superior improvements in range of motion, reduce muscle stiffness, and enhance functional performance.Although both DN and PFS are effective in reducing pain and improving flexibility, they operate through distinct physiological mechanisms. PFS primarily modulates neuromuscular tone through voluntary contraction and reflex inhibition, whereas DN directly targets localized myofascial dysfunction to interrupt pain cycles and restore tissue perfusion. Despite their individual benefits, limited evidence exists directly comparing these two interventions within a standardized rehabilitation framework for chronic non-specific low back pain associated with hamstring tightness.However, no evidence exists comparing post-facilitation stretch and dry needling when combined with conventional physiotherapy in chronic non-specific low back pain associated with hamstring tightness.Therefore, the present randomized clinical trial aims to compare the effects of post-facilitation stretch and dry needling, each combined with conventional physiotherapy treatment, in individuals with chronic non-specific low back pain accompanied by hamstring tightness. The primary objective of the study is to determine which intervention leads to greater improvement in hamstring flexibility. Secondary objectives include comparison of lumbar range of motion, pelvic tilt, pain intensity, and functional disability between the two intervention groups.

Conditions
Low Back Pain
Being tested
Dry Needling along with Conventional Therapy, Post Facilitation Stretch along with Conventional Therapy
Keywords
Chronic Low Back Pain, Dry Needling, Post Facilitation Stretch
Medical subject headings
Low Back Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dry Needling along with Conventional TherapyOther

    Patient in prone position with pillow under ankle. After skin antisepsis, a sterile filiform needle (0.25 × 40 mm) will be inserted into identified myofascial trigger points in the hamstrings. Local twitch responses will be elicited with 5-10 positioning movements. Needle retention 30-60 seconds per point for 3 weeks 3 session per week.The patient was positioned in supine lying on the treatment plinth with the contralateral limb extended and the treated limb raised with the knee extended for static hamstring stretching. The pelvis was stabilized to prevent compensatory movements.For the moist heat pack, the patient remained in prone lying, with the heat pack applied over the posterior thigh (hamstring region) and properly secured for comfort and safety

  • Post Facilitation Stretch along with Conventional TherapyOther

    Post-Facilitation Stretch with Conventional Physiotherapy. Participants in this group will receive post-facilitation stretch combined with conventional physiotherapy. Post-facilitation stretch will be performed with the patient in supine lying. The therapist will passively stretch the hamstring muscle to the point of first resistance, followed by a maximal isometric contraction (100% effort) for 7-10 seconds. After a brief relaxation period of 1-2 seconds, a rapid, controlled stretch will be applied and held for 15-20 seconds. This sequence will be repeated 3-5 times per session. Conventional physiotherapy will include a 5-minute moist heat pack applied to the posterior thigh before treatment, followed by static hamstring stretching (3 repetitions × 20 seconds) after the session. Sessions will be conducted three times per week for 3 weeks, with a total of 9 sessions, each session lasting approximately 30 minutes.

Study groups in NCT07426562
Study groupRoleWhat they receive
Dry Needling along with Conventional TherapyActive comparatorNeedle retention 30-60 seconds per point. 5 minute moist heat pack applied to posterior thigh before treatment Static hamstring stretches 3 reps × 20 seconds post-session.
Receives: Other: Dry Needling along with Conventional Therapy
Post-Facilitation Stretch along with Conventional PhysiotherapyActive comparatormaximal isometric contraction for 7-10 seconds, followed by complete relaxation for 1-2 seconds, rapid, controlled stretch for 15-20 seconds 3-5 reps 5-minute moist heat pack Static hamstring stretches 3 reps × 20 seconds post-session.
Receives: Other: Post Facilitation Stretch along with Conventional Therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Hamstring Flexibility (Active Knee Extension Test)

    Changes from baseline hamstring flexibility will be assessed using the Active Knee Extension (AKE) test measured with a universal goniometer. The AKE test evaluates hamstring extensibility by measuring the degree of active knee extension with the hip maintained at 90° flexion. It is a reliable and valid clinical measure for assessing hamstring tightness in individuals with low back pain.

    Measured: baseline,1 week, 2 week, 3 week

Secondary outcomes (4)
  1. Numeric Pain Rating Scale (NPRS)

    Changes from Baseline pain values will be taken with the help of Numeric Pain Rating Scale measures level of pain. Scoring is done by selecting a point from zero to ten as the current level of pain. Zero means minimum pain and 10 denotes maximum pain.

    Measured: Baseline, 1 week, 2 week, 3 week

  2. Lumbar Range of Motion

    Changes from baseline lumbar flexion and extension range of motion will be measured using a universal goniometer following standardized assessment procedures with the participant in standing position.

    Measured: Baeline ,1 week, 2 week, 3 week

  3. Pelvic Tilt

    Changes from baseline pelvic alignment will be assessed using a pelvic inclinometer by measuring the angle between the anterior superior iliac spine (ASIS) and posterior superior iliac spine (PSIS). This measure provides an objective assessment of anterior or posterior pelvic tilt.

    Measured: Baeline, 1 week, 2 week, 3 week

  4. Functional Disability (Modified Oswestry Disability Index MODI)

    Changes from baseline functional disability will be assessed using the Modified Oswestry Disability Index (MODI). MODI is a validated questionnaire used to evaluate the impact of low back pain on daily activities and functional status, with higher scores indicating greater disability.

    Measured: Baeline, 1 week, 2 week, 3 week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Feb 2026
  2. Study start2 Feb 2026
  3. Primary completion31 Jul 2026 (estimated)
  4. Study completion31 Aug 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
36 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07426562
Sponsor's protocol ID
RCRAHS-ISB/REC/MS-PT024437
Status last verified
Jul 2026
First submitted
17 Feb 2026
Last updated
20 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Dry Needling along with Conventional Therapy and Post Facilitation Stretch along with Conventional Therapy in people with Low Back Pain, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Imran Amjad PT, PhD (03324390125, imran.amjad@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Hamstring Flexibility (Active Knee Extension Test) (time frame: baseline,1 week, 2 week, 3 week). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jul 2026.

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