AzTrials
AzTrials

Low Back PainNCT07627581

Foam Roller Versus Self-Performed Neurodynamic Sliding in People With Hamstring Tightness and Low Back Pain History

A study testing Self-Myofascial Release Using a Foam Roller and Self-Administered Neurodynamic Sliding Technique in people with Low Back Pain and Hamstring Tightness, run by Universidad Pontificia de Salamanca at 1 site in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This randomized crossover pilot clinical trial evaluated the effects of two self-administered physiotherapy techniques in people with hamstring tightness and a history of non-specific low back pain. Participants were randomly assigned to one of two treatment sequences. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Low Back Pain, Hamstring Tightness
What is being tested?
Self-Myofascial Release Using a Foam Roller and Self-Administered Neurodynamic Sliding Technique
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteSpain
Study dates
2 Jun 2026to 10 Sep 2026
Phase
Interventional
Are there results?
None posted in the registry

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 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Men and women aged 16 years or older.
  • History of non-specific low back pain during the previous three months and/or recurrent or chronic non-specific low back pain.
  • Limited hamstring flexibility, defined as hamstring tightness with 75 degrees or less of hip flexion with knee extension during the Straight Leg Raise test.
  • No previous surgery involving the spine or lower limb.
  • No hamstring stretching exercises performed in the weeks prior to participation.
  • Ability and willingness to provide informed consent.
  • Availability to perform both self-administered physiotherapy techniques according to the study protocol.

Who cannot join

  • Pregnancy or breastfeeding.
  • History of hamstring muscle or tendon injury during the previous year.
  • Lumbar or lower-limb neurological deficits.
  • Lower-limb length discrepancy.
  • Specific spinal pathology, including tumor, infection, fracture, or inflammatory disease.
  • History of lumbar disc herniation.
Show all 14Show fewer
  • History of whiplash injury.
  • Any contraindication to physical exercise.
  • Menstrual pain at the time of assessment or intervention.
  • Scheduled surgery during the intervention or follow-up period.
  • History of cardiac disease.
  • Incomplete or incorrectly completed questionnaires or missing assessment data.
  • Refusal to complete part or all of the study intervention.
  • Development of a low back pain episode during the study intervention.

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Clínica Universitaria Salus Infirmorum, Universidad Pontificia de Salamanca

    Madrid, Madrid, 28015

Other trials in Spain

About this study

Official title: Effects of Self-Myofascial Release With Foam Roller Versus Self-Performed Neurodynamic Sliding on Hamstring Flexibility in People With Hamstring Tightness and a History of Low Back Pain: A Randomized Pilot Clinical Trial

This randomized crossover pilot clinical trial evaluated the effects of two self-administered physiotherapy techniques in people with hamstring tightness and a history of non-specific low back pain.

Participants were randomly assigned to one of two treatment sequences. One sequence performed self-myofascial release using a foam roller first, followed by a one-month washout period, and then performed a self-administered neurodynamic sliding technique. The other sequence performed the neurodynamic sliding technique first, followed by a one-month washout period, and then performed the foam roller intervention.

The main objective of the study was to compare the effects of both interventions on hamstring flexibility. Secondary outcomes included active knee extension range of motion, dynamic balance, pressure pain threshold, hamstring and gluteus maximus strength, and low back pain intensity.

Read the detailed description

Low back pain is a common musculoskeletal condition, and hamstring tightness has been proposed as a potential contributing factor due to its influence on pelvic and lumbar biomechanics. Different physiotherapy interventions may be used to improve hamstring flexibility, including self-myofascial release with a foam roller and neurodynamic sliding techniques.

This study was designed as a randomized, crossover, pilot clinical trial with two active interventions. Participants were people with hamstring tightness and a history of recurrent or chronic non-specific low back pain. Eligible participants were randomly assigned to one of two intervention sequences.

In one sequence, participants first performed self-myofascial release using a foam roller on the hamstring muscles. After a one-month washout period, they then performed the self-administered neurodynamic sliding technique. In the other sequence, participants first performed the self-administered neurodynamic sliding technique. After a one-month washout period, they then performed the self-myofascial release intervention using a foam roller.

The foam roller intervention consisted of bilateral self-myofascial release of the hamstring muscles for 2 minutes per leg over three consecutive days. The neurodynamic sliding intervention consisted of a seated self-administered neurodynamic sliding technique over three consecutive days, with 3 sets of 20 repetitions and 20 seconds of rest between sets.

Assessments were performed before and after each intervention period. The primary outcome was hamstring flexibility measured using the Straight Leg Raising test. Secondary outcomes included hamstring flexibility measured using the Active Knee Extension test, dynamic balance assessed with the Y-Balance Test, pressure pain threshold over myofascial trigger points, isometric strength of the hamstrings and gluteus maximus, and low back pain intensity measured with the Numeric Pain Rating Scale.

Being tested
Self-Myofascial Release Using a Foam Roller, Self-Administered Neurodynamic Sliding Technique
Keywords
foam roller, Self-myofascial release, Neurodynamic sliding, Hamstring flexibility, Low back pain, Crossover trial
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.

  • Self-Myofascial Release Using a Foam RollerOther

    Participants will perform bilateral self-myofascial release of the hamstring muscles using a foam roller. The technique will be performed for 2 minutes per leg over three consecutive days.

  • Self-Administered Neurodynamic Sliding TechniqueOther

    Participants will perform a seated self-administered neurodynamic sliding technique over three consecutive days. The intervention will consist of 3 sets of 20 repetitions, with 20 seconds of rest between sets.

Study groups in NCT07627581
Study groupRoleWhat they receive
Foam Roller First, Then Neurodynamic SlidingExperimentalParticipants assigned to this sequence will first perform self-myofascial release using a foam roller on the hamstring muscles. After a one-month washout period, they will perform the self-administered neurodynamic sliding technique.
Receives: Other: Self-Myofascial Release Using a Foam Roller; Other: Self-Administered Neurodynamic Sliding Technique
Neurodynamic Sliding First, Then Foam RollerExperimentalParticipants assigned to this sequence will first perform the self-administered neurodynamic sliding technique. After a one-month washout period, they will perform self-myofascial release using a foam roller on the hamstring muscles.
Receives: Other: Self-Myofascial Release Using a Foam Roller; Other: Self-Administered Neurodynamic Sliding Technique

What is being measured

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

  1. Change in Hamstring Flexibility Measured With the Straight Leg Raise Test

    Hamstring flexibility will be assessed using the Straight Leg Raise test. The test will be performed with the participant in the supine position, and hip flexion range of motion will be measured in degrees using a goniometer. Higher values indicate greater hamstring flexibility.

    Measured: Baseline of each intervention period, 24 hours after completing each intervention, and 7 days after each intervention

Secondary outcomes (4)
  1. Change in Hamstring Flexibility Measured With the Active Knee Extension Test

    Hamstring flexibility will be assessed using the Active Knee Extension test. The knee extension angle will be measured in degrees using a goniometer, with the hip positioned at 90 degrees of flexion.

    Measured: Baseline of each intervention period, 24 hours after completing each intervention, and 7 days after each intervention

  2. Change in Dynamic Balance Measured With the Y-Balance Test

    Dynamic balance will be assessed using the Y-Balance Test. Reach distances in the anterior, posteromedial, and posterolateral directions will be recorded in centimeters and normalized to lower limb length.

    Measured: Baseline of each intervention period, 24 hours after completing each intervention, and 7 days after each intervention

  3. Change in Pressure Pain Threshold

    Isometric strength of the hamstring muscles and gluteus maximus will be assessed using a handheld dynamometer. Values will be recorded in Newtons, with higher values indicating greater muscle strength.

    Measured: Baseline of each intervention period, 24 hours after completing each intervention, and 7 days after each intervention

  4. Change in Low Back Pain Intensity

    Low back pain intensity will be assessed using the Numeric Pain Rating Scale, ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain.

    Measured: Baseline of each intervention period, 24 hours after completing each intervention, and 7 days after each intervention

Timeline

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

  1. First posted4 Jun 2026
  2. Study start2 Jun 2026
  3. Primary completion12 Jul 2026
  4. Study completion10 Sep 2026

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
Crossover
Model description
Participants will be randomly assigned to one of two intervention sequences. In one sequence, participants will first perform self-myofascial release using a foam roller, followed by a one-month washout period, and then perform the self-administered neurodynamic sliding technique. In the other sequence, participants will first perform the self-administered neurodynamic sliding technique, followed by a one-month washout period, and then perform self-myofascial release using a foam roller.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07627581
Sponsor's protocol ID
UPSA_HAM_LBP
Status last verified
Sep 2026
First submitted
30 May 2026
Last updated
29 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared because the study dataset contains health-related information collected in a small pilot trial. Data will be pseudonymized and stored according to applicable data protection regulations, but no formal data sharing plan has been established.

Questions about this trial

What is this clinical trial studying?

A study testing Self-Myofascial Release Using a Foam Roller and Self-Administered Neurodynamic Sliding Technique in people with Low Back Pain and Hamstring Tightness, run by Universidad Pontificia de Salamanca at 1 site in Spain.

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 7 inclusion and 14 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: finished, as of the sponsor's last update on 29 Sep 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 Spain. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Hamstring Flexibility Measured With the Straight Leg Raise Test (time frame: Baseline of each intervention period, 24 hours after completing each intervention, and 7 days after each intervention). 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 29 Sep 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in