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Sports Physical TherapyNCT05134883

PNF Stretching Compared to SMR on Hamstrings

A study testing PNF and SMR in people with Sports Physical Therapy, run by Universitat Internacional de Catalunya at 1 site in Spain.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The use of stretching techniques in the sports world is frequent and widely used for its many effects. One of the main benefits is the gain in flexibility, range of motion and facilitation of the sporting performance. Read more about this study

Who is it for?
Ages 18 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Sports Physical Therapy
What is being tested?
PNF and SMR
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteSpain
Study dates
5 Oct 2021to 30 Jan 2022
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 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • -

Who cannot join

  • hypermobility
  • hamstring injury in the previous 6 months
  • diagnosed orthopedic problems
  • surgery in the lower limbs
  • back pain
  • spine surgery
  • systemic or neurological disorders.

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Universitat Internacional Catalunya

    Barcelona, Sant Cugat, 08195

Other trials in Spain

About this study

Official title: Effects of Hamstrings Flexibility After Proprioceptive Neuromuscular Facilitation Stretching Compared to Self-myofascial Release: a Randomized Controlled Trial

The use of stretching techniques in the sports world is frequent and widely used for its many effects. One of the main benefits is the gain in flexibility, range of motion and facilitation of the sporting performance. Recently the use of self-myofascial release (SMR) has spread in sports practice both at elite and recreational level for its benefits being similar to those observed in stretching. The objective of the following study is to compare the results of the proprioceptive neuromuscular facilitation stretching with SMR on the hamstring muscle flexibility.

Being tested
PNF, SMR
Keywords
Stretching, Propioceptive neuromuscular facilitation, Hamstrings

What participants receive

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

  • PNFOther

    A PNF stretching protocol will be performed with each participant assuming a long sitting position on a plinth with the knee maintained as extended as possible. At this moment, the participant will be asked to perform a maximum isometric hamstring muscle contraction for 5 seconds followed by 5 seconds of relaxation and 20 seconds of stretching. The therapist will show the participant how to maintain this isometric contraction with the flexion of the hip and ankle. Each participant will undergo 4 repetitions of PNF stretching (30 seconds/rep).

  • SMROther

    For the application of self-myofascial release, the subjects will assume a long sitting position on a firm and even surface by placing the arms backward and transferring their body weight to their palms. The roller foam, applied bilaterally, will be placed under the hamstrings and slowly moved back and forth from the ischial tuberosity to the popliteal fossa by applying pressure for 2 minutes.

Study groups in NCT05134883
Study groupRoleWhat they receive
Propioceptive neuromuscular facilitation (PNF)ExperimentalThis group will undergo a PNF stretching on the hamstring muscles.
Receives: Other: PNF
self myo-fascial release (SMR)Active comparatorThis group will undergo a SMR stretching on the hamstring muscles.
Receives: Other: SMR

What is being measured

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

  1. Hamstring muscle flexibility (mm)

    Evaluated with a modified sit-and-reach test (MSR). The participants sit on the floor with their lower limbs stretched out and together, their backs and hips are supported against the wall (90° hip flexion), and the soles of their feet are placed against the edge of a box. Participants then extended their arms forward, placing the same hand on top of the other with both hands facing down. During this, they keep their backs against the wall. They then reach forward, sliding their hands along the measuring scale as far as possible without bending their knees

    Measured: Change between baseline(immediately before intervention), mid-intervention (30 seconds after the start of the intervention) and post intervention (2 minutes after the start of the intervention)

Secondary outcomes (1)
  1. Discomfort sensation

    Measured using the Borg rating of perceived exertion scale (RPE). The participants will be asked at the end of the intervention to give a number from 1 to 10, where 1 is the easiest and 10 the hardest.

    Measured: Change between baseline(immediately before intervention), mid-intervention (30 seconds after start of intervention) and post intervention (2 minutes after the start of the intervention)

Timeline

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

  1. First posted26 Nov 2021
  2. Study start5 Oct 2021
  3. Primary completion25 Oct 2021
  4. Study completion30 Jan 2022 (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
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05134883
Sponsor's protocol ID
PNF_01
Status last verified
Nov 2021
First submitted
12 Oct 2021
Last updated
26 Nov 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Perez-Bellmunt A, Casasayas-Cos O, Ragazzi P, Rodriguez-Sanz J, Hidalgo-Garcia C, Canet-Vintro M, Caballero-Martinez I, Pacheco L, Lopez-de-Celis C. Foam Rolling vs. Proprioceptive Neuromuscular Facilitation Stretching in the Hamstring Flexibility of Amateur Athletes: Control Trials. Int J Environ Res Public Health. 2023 Jan 12;20(2):1439. doi: 10.3390/ijerph20021439.

    PubMed 36674197

Questions about this trial

What is this clinical trial studying?

A study testing PNF and SMR in people with Sports Physical Therapy, run by Universitat Internacional de Catalunya 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 1 inclusion and 7 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: status not confirmed, as of the sponsor's last update on 26 Nov 2021. 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?

Results are not available in the source record.

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?

Hamstring muscle flexibility (mm) (time frame: Change between baseline(immediately before intervention), mid-intervention (30 seconds after the start of the intervention) and post intervention (2 minutes after the start of the intervention)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05134883, which also lists 1 linked publication.

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 26 Nov 2021; AzTrials last refreshed its copy on 30 Oct 2026.

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