- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07688850
Effect of Three Force Magnitudes During the Cross-Hand Technique in the Thoracolumbar Region on the Myofascial System in Healthy Adults (MFR)
June 30, 2026 updated by: Universidad de la Sabana
Orthopedic Manual Therapy (OMT) employs specific manual techniques to assess and treat musculoskeletal dysfunctions.
Among these, the Myofascial Induction Method (MIM) and its "crossed hands" technique are designed to restore fascial mobility and hydration through sustained mechanical forces.
However, the lack of standardization (particularly regarding applied force) limits reproducibility and clinical consistency.
The objective of this research is to compare the effects of three force magnitudes (2 kg, 5 kg, and 11 kg) applied during the crossed-hands technique on fascial stiffness, thickness, pain pressure threshold, and lumbopelvic mobility in healthy adults.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Introduction: Orthopedic Manual Therapy (OMT) employs specific manual techniques to assess and treat musculoskeletal dysfunctions.
Among these, the Myofascial Induction Method (MIM) and its "crossed hands" technique are designed to restore fascial mobility and hydration through sustained mechanical forces.
However, the lack of standardization (particularly regarding applied force) limits reproducibility and clinical consistency.
Objective: To compare the effects of three force magnitudes (2 kg, 5 kg, and 11 kg) applied during the crossed-hands technique on fascial stiffness, thickness, pain pressure threshold, and lumbopelvic mobility in healthy adults.
Methods: A quasi-experimental study was conducted with 30 healthy participants, divided into three groups (n = 10 each).
Each received a single 5-minute session of the crossed-hands technique on the thoracolumbar fascia using forces of 2 kg (G3), 5 kg (G2), or 11 kg (G1).
Fascial stiffness was measured with a Shore 00 durometer, thickness via ultrasound (Mindray TE7), pain pressure threshold (PPT) by algometry, and lumbopelvic mobility using Kinovea® motion analysis.
Study Type
Interventional
Enrollment (Actual)
30
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
-
-
-
Chía, Colombia, 25001
- Universidad de La Sabana
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Participants aged 18 years or older
- Participants of both sexes
- Apparently healthy participants
Exclusion Criteria:
- Individuals with cognitive disability that limited the ability to follow instructions
- Participants with active pain greater than 5/10 at the time of the examination
- Participants with obesity (BMI greater than 30)
- Individuals with active vertigo
- Participants taking muscle relaxants at the time of the measurement,
- Participants who had received myofascial induction within 24 hours prior to the measurement
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: Screening
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 2kg
This group received a single 5-minute session of the crossed-hands technique on the thoracolumbar fascia using forces of 2 kg measured by a adapated stretcher with loan cells
|
Crossed hands technique.
This approach is based on stimulating the myofascial system through the application of slow and gradual pressures.
Its objective is to restore hydration and release deep restrictions within the soft tissue that cannot be reached with direct pressure or are difficult to identify during the initial evaluation process
|
|
Experimental: 5kgs
This group received a single 5-minute session of the crossed-hands technique on the thoracolumbar fascia using forces of 5 kg measured by a adapated stretcher with loan cells
|
Crossed hands technique.
This approach is based on stimulating the myofascial system through the application of slow and gradual pressures.
Its objective is to restore hydration and release deep restrictions within the soft tissue that cannot be reached with direct pressure or are difficult to identify during the initial evaluation process
|
|
Experimental: 11Kgs
This group received a single 5-minute session of the crossed-hands technique on the thoracolumbar fascia using forces of 11 kg measured by a adapated stretcher with loan cells
|
Crossed hands technique.
This approach is based on stimulating the myofascial system through the application of slow and gradual pressures.
Its objective is to restore hydration and release deep restrictions within the soft tissue that cannot be reached with direct pressure or are difficult to identify during the initial evaluation process
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pelvic mobility
Time Frame: This variable will be measured before the intervention and inmediatly after the intervention, all in the same day.
|
Subjects will be placed in a standing position and instructed to touch the floor with their hands while keeping their knees extended.
The variables analyzed are anterior pelvic tilt and the translation angle of the lower limbs
|
This variable will be measured before the intervention and inmediatly after the intervention, all in the same day.
|
|
Fascial stiffness
Time Frame: This variable will be measured before the intervention and inmediatly after the intervention, all in the same day.
|
Fascial stiffness is the mechanical property of fascial tissue that reflects its resistance to changes in shape or length when subjected to an external force.
It is influenced by the composition and organization of the extracellular matrix, collagen fiber arrangement, tissue hydration, and neuromuscular factors.
|
This variable will be measured before the intervention and inmediatly after the intervention, all in the same day.
|
|
pressure pain threshold (PPT)
Time Frame: This variable will be measured before the intervention and inmediatly after the intervention, all in the same day.
|
Pressure Pain Threshold (PPT) is defined as the minimum amount of pressure applied to a tissue that is perceived as painful by an individual.
|
This variable will be measured before the intervention and inmediatly after the intervention, all in the same day.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Alejandra Sánchez, PT, Universidad de La Sabana
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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)
June 5, 2025
Primary Completion (Actual)
September 28, 2025
Study Completion (Actual)
September 29, 2025
Study Registration Dates
First Submitted
June 24, 2026
First Submitted That Met QC Criteria
June 30, 2026
First Posted (Actual)
July 7, 2026
Study Record Updates
Last Update Posted (Actual)
July 7, 2026
Last Update Submitted That Met QC Criteria
June 30, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FIS2026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
I can not share personal data of the participants due to the limitations given by the ethics commite
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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