- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05134883
PNF Stretching Compared to SMR on Hamstrings
November 23, 2021 updated by: Albert Pérez Bellmunt, Universitat Internacional de Catalunya
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.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
80
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sant Cugat
-
Barcelona, Sant Cugat, Spain, 08195
- Universitat Internacional Catalunya
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
-
Exclusion Criteria:
- hypermobility
- hamstring injury in the previous 6 months
- diagnosed orthopedic problems
- surgery in the lower limbs
- back pain
- spine surgery
- systemic or neurological disorders.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Propioceptive neuromuscular facilitation (PNF)
This group will undergo a PNF stretching on the hamstring muscles.
|
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).
|
|
Active Comparator: self myo-fascial release (SMR)
This group will undergo a SMR stretching on the hamstring muscles.
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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)
|
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
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Discomfort sensation
Time Frame: 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)
|
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.
|
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)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Albert Pérez-Bellmunt, PhD, Universitat International Catalunya
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 5, 2021
Primary Completion (Actual)
October 25, 2021
Study Completion (Anticipated)
January 30, 2022
Study Registration Dates
First Submitted
October 12, 2021
First Submitted That Met QC Criteria
November 23, 2021
First Posted (Actual)
November 26, 2021
Study Record Updates
Last Update Posted (Actual)
November 26, 2021
Last Update Submitted That Met QC Criteria
November 23, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- PNF_01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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