FasciaNCT05711745
Effects of Myofascial Induction Therapy on Pressure Pain and Ankle Range of Motion.
A study testing Calf myofascial technique in people with Fascia and Trigger Point Pain, Myofascial, run by Mayuben Private Clinic at 1 site in Spain.
Trial summary
In this study, it will be assessed if there are changes in ankle dorsiflexion and pressure pain after performing the myofascial induction technique in the calf. Read more about this study
- Who is it for?
- Ages 18 to 30 yearsHealthy volunteers can take part
- Conditions the study is for
- Fascia, Trigger Point Pain, Myofascial, Range of Motion
- What is being tested?
- Calf myofascial technique
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 10 participants
- Where
- 1 siteSpain
- Study dates
- 6 Feb 2023to 9 Feb 2023
- 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 30 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Subjects with no pain and with 18 to 30 years old.
Who cannot join
- (1) Diagnosis of lower limb injury, including any tendinopathy, bursitis, ligamentous involvement or fasciitis ,
- (2) history of lower limb surgery ,
- (3) participants were required not to have undergone ankle stretching or any other treatment,
- (4) diabetes due to possible alteration of arterial distal circulation,
- (5) deformities of the toes, such as hammer toes and hallux valgus. All subjects signed an informed consent form before participating in the study
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effects of Myofascial Induction Therapy on Ankle Pressure Pain and Ankle Range of Motion in Latent Trigger Points of the Gastrocnemius Muscle. A Clinical Trial.
In this study, it will be assessed if there are changes in ankle dorsiflexion and pressure pain after performing the myofascial induction technique in the calf.
- Conditions
- Fascia, Trigger Point Pain, Myofascial, Range of Motion, Pain
- Being tested
- Calf myofascial technique
- Medical subject headings
- Myofascial Pain Syndromes, Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Calf myofascial techniqueProcedure or surgery
A 3-pass superficial leg glide technique was applied first and then 5 minutes of the deep calf myofascial induction technique as described by Pilat.
| Study group | Role | What they receive |
|---|---|---|
| Myofascial induction in gastrocnemius | Experimental | A 3-pass superficial leg glide technique was applied first and then 5 minutes of the deep calf myofascial induction technique as described by Pilat. Receives: Procedure: Calf myofascial technique |
What is being measured
The primary outcome is the main question the study is designed to answer.
Pressure pain threshold
The pressure at which the patient begins to feel pain with pressure is measured 3 times with an algometer.It is measured in newtons
Measured: Immediately before intervention.
Range of motion with knee extended
The joint range is measured in dorsiflexion of the ankle joint with the knee extended under load and is measured with an inclinometer in degrees.Measured in grades.
Measured: Immediately before the intervention.
Range of motion with knee flexed
The joint range is measured in dorsiflexion of the ankle joint with the knee flexed under load and is measured with an inclinometer in degrees. Measured in grades.
Measured: Immediately before the intervention.
Pressure pain threshold
The pressure at which the patient begins to feel pain with pressure is measured 3 times with an algometer.It is measured in newtons
Measured: Immediately after the intervention.
Range of motion with knee extended
The joint range is measured in dorsiflexion of the ankle joint with the knee extended under load and is measured with an inclinometer in degrees.Measured in grades.
Measured: Immediately after the intervention.
Range of motion with knee flexed
The joint range is measured in dorsiflexion of the ankle joint with the knee flexed under load and is measured with an inclinometer in degrees.Measured in grades.
Measured: Immediately after the intervention.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Feb 2023
- Study start6 Feb 2023
- Primary completion8 Feb 2023
- Study completion9 Feb 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for FasciaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Not applicable
- Intervention model
- Single group
- Model description
- A pre-post study
- Masking
- None (open label)
- Enrolment
- 10 participants (actual)
Sponsor and investigators
- Lead sponsor
- Mayuben Private Clinic
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, EVA MARIA MARTÍNEZ JIMENEZ, Mayuben Private Clinic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05711745
- Sponsor's protocol ID
- 2911202021420A
- Status last verified
- Feb 2023
- First submitted
- 16 Jan 2023
- Last updated
- 10 Feb 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Feb 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Myofascial Induction Therapy on Ankle Pressure Pain and Ankle Range of Motion in Latent Trigger Points of the Gastrocnemius Muscle. A Clinical Trial.
- ClinicalTrials.gov ID
- NCT05711745
- Acronym / sponsor ID
- 2911202021420A
- Conditions
- Fascia, Trigger Point Pain, Myofascial, Range of Motion, Pain
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 10 participants (actual)
- Lead sponsor
- Mayuben Private ClinicUniversity, hospital or other
- Study start
- 6 Feb 2023 (actual)
- Primary completion
- 8 Feb 2023 (actual)
- Study completion
- 9 Feb 2023 (actual)
- First posted
- 3 Feb 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
In this study, it will be assessed if there are changes in ankle dorsiflexion and pressure pain after performing the myofascial induction technique in the calf.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- A pre-post study
| Arm | Type | Receives |
|---|---|---|
| Myofascial induction in gastrocnemius | Experimental | Procedure: Calf myofascial techniqueA 3-pass superficial leg glide technique was applied first and then 5 minutes of the deep calf myofascial induction technique as described by Pilat. |
Who may qualify
- Ages
- 18 to 30 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- Subjects with no pain and with 18 to 30 years old.
Key exclusion criteria (5 listed)
- (1) Diagnosis of lower limb injury, including any tendinopathy, bursitis, ligamentous involvement or fasciitis ,
- (2) history of lower limb surgery ,
- (3) participants were required not to have undergone ankle stretching or any other treatment,
- (4) diabetes due to possible alteration of arterial distal circulation,
- (5) deformities of the toes, such as hammer toes and hallux valgus. All subjects signed an informed consent form before participating in the study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Calf myofascial techniqueA 3-pass superficial leg glide technique was applied first and then 5 minutes of the deep calf myofascial induction technique as described by Pilat. | Procedure or surgery | Myofascial induction in gastrocnemius |
Primary outcome
Pressure pain threshold
Time frame: Immediately before intervention.
The pressure at which the patient begins to feel pain with pressure is measured 3 times with an algometer.It is measured in newtons
Range of motion with knee extended
Time frame: Immediately before the intervention.
The joint range is measured in dorsiflexion of the ankle joint with the knee extended under load and is measured with an inclinometer in degrees.Measured in grades.
Range of motion with knee flexed
Time frame: Immediately before the intervention.
The joint range is measured in dorsiflexion of the ankle joint with the knee flexed under load and is measured with an inclinometer in degrees. Measured in grades.
Pressure pain threshold
Time frame: Immediately after the intervention.
The pressure at which the patient begins to feel pain with pressure is measured 3 times with an algometer.It is measured in newtons
Range of motion with knee extended
Time frame: Immediately after the intervention.
The joint range is measured in dorsiflexion of the ankle joint with the knee extended under load and is measured with an inclinometer in degrees.Measured in grades.
Range of motion with knee flexed
Time frame: Immediately after the intervention.
The joint range is measured in dorsiflexion of the ankle joint with the knee flexed under load and is measured with an inclinometer in degrees.Measured in grades.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Feb 2023.
- Individual participant dataSharing planned: No
Related trials for Fascia
Not yet recruiting
Effect of Lumbar Stabilization Exercises With and Without YTWL (Scapular Stabilization Exercises) on Reducing Chronic Low Back Pain and Related Disability. A Randomized Clinical Trial,
Chronic Non Specific Mechanical Low Back Pain
RecruitingPhase 2
REctus Sheath Trial
Acute Pain, Postoperative Pain, Acute
Recruiting
Effectiveness of Pulsed Electromagnetic Field Therapy in Patients With Symptomatic Plantar Calcaneal Spurs
Calcaneal Spur
Active, not recruiting
Lumbar-Sacral Plexus Block vs Fascia Iliaca Block Plus Low-Dose Spinal Anesthesia for Femoral Neck Fracture Surgery
Femoral Neck Fractures, Nerve Block
Not yet recruitingObservational study
Relationship Between Disability, Flexibility, Back Muscles, and Thoracolumbar Fascia in Patients With Lumbar Disc Degeneration
Intervertebral Disc Degeneration
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Calf myofascial technique in people with Fascia and Trigger Point Pain, Myofascial, run by Mayuben Private Clinic 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 5 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 10 Feb 2023. 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?
Pressure pain threshold (time frame: Immediately before intervention.). The study lists 6 primary outcomes in all. 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 10 Feb 2023.