- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04404829
Informational Manual Therapy to Improve Standing Balance
The Effect of the Informational Manual Therapy for Improving Quiet Standing, Pain and Quality of Life in Healthy Individuals
Objectives: The aim of this study is to assess the effect of Informational Manual Therapy (IMT) on quiet standing and quality of life in healthy individuals. The IMT also is known as the Poyet-Pialoux method, is a holistic, no orthopedic, and soft manual therapy.
Design: This is a one-group pretest-posttest design. It is a within-subjects experiment in which each participant is tested first under the control condition and then under the treatment condition.
Setting: University laboratory. Intervention: One IMT session was performed on 57 healthy individuals aged from 18 to 65 years. They were grouped into three age groups. The treatment session was performed by 5 therapists on two days. The primary outcome was quite standing assessed by the SATEL force platform. Secondary outcomes were bodily pain assessed by the pain sections of the 36-Item Short Form Survey (SF-36) and quality of life by EQ-5D-3L (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression). The primary outcome was evaluated before and immediately after treatment and after 7-10 days. The secondary outcomes were assessed after treatment and 3 weeks later.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Methods Study Design: The study has a one-group pretest-posttest design. The personal data of individuals were kept confidential and the data were shared anonymously upon request from the principal researcher. The TREND statement will be followed.
Subjects Fifty-seven participants will be recruited to participate in this study; the sample was one of convenience. The inclusion and exclusion criteria are as follows: age from 18 to 65 years old, not having a positive diagnosis for any disease which influences balance, no participation in any other trial, not suffering from an injury in the 3 months before the study or fractures in the previous 6 months, and no falls in the previous month. All individuals provided informed consent before enrolment.
Intervention All the participants received a single session of 30-45 min of IMT. All the treatment sessions took place at the UIC laboratory. The IMT session was performed over two days by four physiotherapists and a doctor. All have more than five years of experience in IMT treatment.
The first level of IMT was treated in this study: the objective is to harmonize the Cranio-sacral and sacro-pelvic systems, as this is fundamental for maintaining good posture. The first therapeutic maneuvers should be focused on releasing of the sacrum and the pelvis. The first is considered a key area for the correct transmission of forces and loads from the lower limbs to the upper limbs and vice versa and shares the role of rigid elements for this purpose (bones) and tensile elements (muscles, ligaments, fascia) in the whole body. At this level. Compensatory injuries that the body has started after a primary injury are treated on this level, through the Fluidic Chains. This also includes the treatment of some traumatic injuries, such as cranial strains, the compression of spheno-basilar synchondrosis, injuries of the pelvis and occipital bone, and damage to the flexion-extension and lateral displacement of the vertebrae. The diagnosis of this level is performed by cranial somotopias (reflex points on the skull and face). Practically all the treatment is carried out on the sacrum. The first step is the "fuses," which are vibration zones that act as a protection system for the body (1). These points sometimes stop working, which interrupts the correct movement of the PRM: 1st fuse: Inn-trang (on the forehead between the two eyebrows, the 4th sacral vertebra is stimulated if it is not adjusted). A massage on the scalp in several very soft circles that goes from the frontal to the occipital area is performed 6 times. 2nd fuse: 1st dorsal vertebra, 4th cervical, 4th dorsal, and 3rd lumbar. 3rd fuse: C0 (base of the occipital), a zone of the 2nd sacral vertebra, and the space between the spines of the 2nd and 3rd dorsal vertebrae and finally point R1 (between the 2nd and 3 rd metatarsal). If any point is blocked it is treated and harmonized with a soft touch towards the occipital.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Catalonia
-
Barcelona, Catalonia, Spain, 08195
- Universitat Internacional de Catalunya
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Healthy people
Exclusion Criteria:
Not having problems with balance, Not suffering from an injury in the 3 months before the study, Not suffering from a fracture in the previous 6 month before the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Informational Manual Therapy
It is an integral no orthopedic and very soft manual therapy
|
The first level of IMT was treated in this study: the objective is to harmonize the cranio-sacral and sacro-pelvic systems, as this is fundamental for maintaining good posture.
The first therapeutic maneuvers should be focused on releasing of the sacrum and the pelvis.
The first is considered a key area for the correct transmission of forces and loads from the lower limbs to the upper limbs and vice versa and shares the role of rigid elements for this purpose (bones) and tensile elements (muscles, ligaments, fascia) in the whole body.
In this level.
Compensatory injuries that the body has started after a primary injury are treated on this level, through the Fluidic Chains.
The diagnosis of this level is performed by cranial somotopias.
Practically all the treatment is carried out on the sacrum.
The first step are the "fuses," which are vibration zones which act as a protection system for the body.
These points sometimes stop working, which interrupts the correct movement of the PRM.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
static standing posture
Time Frame: baseline, pre-intervention
|
It was assessed using the force platform Satel 40 Hz model PF2002, software v 33.5 8C (France).
|
baseline, pre-intervention
|
|
static standing posture
Time Frame: immediately after the intervention
|
It was assessed using the force platform Satel 40 Hz model PF2002, software v 33.5 8C (France).
|
immediately after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
How much bodily pain have you had during the past 4 weeks?
Time Frame: baseline, pre-intervention
|
by the 36-Item Short Form Survey (SF-36). 1 - None,2 - Very mild,3 - Mild, 4 - Moderate, 5 - Severe, - 6 very severe
|
baseline, pre-intervention
|
|
How much bodily pain have you had during the past 4 weeks?
Time Frame: three weeks, post-intervention
|
by the 36-Item Short Form Survey (SF-36). 1 - None,2 - Very mild,3 - Mild, 4 - Moderate, 5 - Severe, - 6 very severe
|
three weeks, post-intervention
|
|
During the past 4 weeks, how much did pain interfere with your normal work (including both work outside the home and housework)?
Time Frame: baseline, pre-intervention
|
by the 36-Item Short Form Survey (SF-36). 1 - Not at all, 2 - A little bit, 3 - Moderately, 4 - Quite a bit, 5 - Extremely
|
baseline, pre-intervention
|
|
During the past 4 weeks, how much did pain interfere with your normal work (including both work outside the home and housework)?
Time Frame: three weeks after treatment
|
by the 36-Item Short Form Survey (SF-36). 1 - Not at all, 2 - A little bit, 3 - Moderately, 4 - Quite a bit, 5 - Extremely
|
three weeks after treatment
|
|
mobility
Time Frame: baseline, pre-intervention
|
by the EQ-5D-3L questionnaire.
Each dimension has 3 levels: no problems, some problems, and extreme problems
|
baseline, pre-intervention
|
|
mobility
Time Frame: three weeks post-intervention
|
by the EQ-5D-3L questionnaire.Each dimension has 3 levels: no problems, some problems, and extreme problems
|
three weeks post-intervention
|
|
self-care
Time Frame: baseline, pre-intervention
|
by the EQ-5D-3L questionnaire.
Each dimension has 3 levels: no problems, some problems, and extreme problems
|
baseline, pre-intervention
|
|
self-care
Time Frame: three weeks post-intervention
|
by the EQ-5D-3L questionnaire.Each dimension has 3 levels: no problems, some problems, and extreme problems
|
three weeks post-intervention
|
|
usual activities
Time Frame: baseline, pre-intervention
|
by the EQ-5D-3L questionnaire.
Each dimension has 3 levels: no problems, some problems, and extreme problems
|
baseline, pre-intervention
|
|
usual activities
Time Frame: three weeks post-intervention
|
by the EQ-5D-3L questionnaire.
Each dimension has 3 levels: no problems, some problems, and extreme problems
|
three weeks post-intervention
|
|
pain/discomfort
Time Frame: baseline, pre-intervention
|
by the EQ-5D-3L questionnaire.
Each dimension has 3 levels: no problems, some problems, and extreme problems
|
baseline, pre-intervention
|
|
pain/discomfort
Time Frame: three weeks post-intervention
|
by the EQ-5D-3L questionnaire.
Each dimension has 3 levels: no problems, some problems, and extreme problems
|
three weeks post-intervention
|
|
anxiety/depression
Time Frame: baseline, pre-intervention
|
by the EQ-5D-3L questionnaire.
Each dimension has 3 levels: no problems, some problems, and extreme problems
|
baseline, pre-intervention
|
|
anxiety/depression
Time Frame: three weeks post-intervention
|
by the EQ-5D-3L questionnaire.
Each dimension has 3 levels: no problems, some problems, and extreme problems
|
three weeks post-intervention
|
|
visual analogue scale for health
Time Frame: baseline, pre-intervention
|
by the EQ-VAS, ranging from 0 ("worst possible") to 100 ("best possible").
|
baseline, pre-intervention
|
|
visual analogue scale for health
Time Frame: three weeks post-intervention
|
by the EQ-VAS, ranging from 0 ("worst possible") to 100 ("best possible").
|
three weeks post-intervention
|
Collaborators and Investigators
Investigators
- Principal Investigator: Rosa Cabanas Valdés, PhD, Universitat Internacional de Catalunya
Publications and helpful links
General Publications
- Bordoni B, Zanier E. Sutherland's legacy in the new millennium: the osteopathic cranial model and modern osteopathy. Adv Mind Body Med. 2015 Spring;29(2):15-21.
- Tseui JJ. Eastern and western approaches to medicine. West J Med. 1978 Jun;128(6):551-7.
- Liem T, Neuhuber W. Osteopathic Treatment Approach to Psychoemotional Trauma by Means of Bifocal Integration. J Am Osteopath Assoc. 2020 Mar 1;120(3):180-189. doi: 10.7556/jaoa.2020.021.
- Lee RP. The living matrix: a model for the primary respiratory mechanism. Explore (NY). 2008 Nov-Dec;4(6):374-8. doi: 10.1016/j.explore.2008.08.003.
- Frymann VM. A study of the rhythmic motions of the living cranium. J Am Osteopath Assoc. 1971 May;70(9):928-45. No abstract available.
- Ballester-Rodes M, Carreras-Costa F, Versyp-Ducaju T, Ballester-Rodes M, Mehta D. Field dynamics in atrioventricular activation. Clinical evidence of a specific field-to-protein interaction. Med Hypotheses. 2019 Mar;124:56-59. doi: 10.1016/j.mehy.2019.02.012. Epub 2019 Feb 2.
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Poyet-Pialoux method
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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