Determine the Effect of the Fourth Ventricle Compression Technique on Physiological Variables
Study Details
Study Description
Brief Summary
This study aims to analyze the influence of the fourth ventricle compression technique in heart rate, respiratory rate, blood pressure, conductivity and thermal variability of the skin in healthy young adults.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
The fourth ventricle compression technique (CV-4) is one of the most important techniques in the treatment of cranial osteopathy.
During the present study, the effects of CV-4 technique will be analyzed in the following variables: heart rate, respiratory rate, blood pressure, conductivity and thermal variation of the skin.
According to the literature, CV-4 technique will cause changes in all of the studied variables, except the respiratory rate, through the activation of the brain stem, namely the parasympathetic nerve centers.
Regarding the respiratory rate, it is justified by the fourth ventricle and the respiratory centers proximity.
Concerning heart rate and respiratory rate, during the CV-4 technique the literature describes a decrease in the values of this variables. However, other studies refer that the technique does not produce relevant effects in the heart and respiratory rates variation, probably because there was no stipulated time to finish the technique, ending subjectively compared to previous ones.
When it comes to blood pressure, a decrease in systolic blood pressure values is noticed by some authors.
In which concerns the variation in body temperature, according to the literature, there were no significant results obtained when performing CV-4.
During the performed literature analysis,there were not found any studies concerning the influences of the CV-4 technique in the thermal conductivity variable.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: CV-4 group The initial selection will be made through a questionnaire, in order to fulfill the exclusion and inclusion criteria. On the data collection day a more detailed survey is performed and informed consent is signed. The patient waits for 5 minutes in the supine position, after which the baseline evaluation is performed. The CV-4 technique is performed following immediate evaluation. 15 minutes after the technique, a new evaluation of the variables is accomplished. |
Other: Fourth ventricle compression technique (CV-4)
The participant is in the supine position and the principal investigator is seated at the patient's head, with elbows resting on the table. The main investigator overlaps his hands with the thenar eminences, contacting the occipital bone squamous part, between the external occipital protuberance and the participant's occipito-mastoid suture. The technique begins with a maintained compression on the occipital squamous part during a deep thorax exhalation. Throughout the compression of the occipital bone and the participant's voluntary inspirations, the principal investigator feels a gradual pressure increase at the thenar eminences. The technique will be performed until reaching the still point, in which the mobility of the occipital bone, respiratory rate and muscle tone decrease, or until 5 minutes elapsed.
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| Sham Comparator: Control group The initial selection will be made through a questionnaire, in order to fulfill the exclusion and inclusion criteria. On the data collection day a more detailed survey is performed and informed consent is signed. The patient waits for 5 minutes in the supine position, after which the baseline evaluation is performed. The sham technique is performed following immediate evaluation. 15 minutes after the technique, a new evaluation of the variables is accomplished. |
Other: Sham
The main investigator uses the technique contact but does not perform any type of tissue traction or compression, maintaining this contact for 5 minutes. At the end of the stipulated time, the contact is removed in a subtle way.
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Outcome Measures
Primary Outcome Measures
- Change from Baseline in heart rate variability immediately after the intervention [Immediately after the intervention.]
To obtain the heart rate measurements, a pulse volume sensor (Biosignalsplux researcher) was connected to the third finger of the hand, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
- Change from Baseline in heart rate variability 15 minutes after the intervention [15 minutes after the intervention.]
To obtain the heart rate measurements, a pulse volume sensor (Biosignalsplux researcher) was connected to the third finger of the hand, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
Secondary Outcome Measures
- Change from Baseline in respiratory rate variability immediately after the intervention [Immediately after the intervention.]
To obtain the respiratory rate measurements, a respiratory belt transducer (Biopac Systems) was adjusted to the patient's thorax, at the xiphoid process level, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
- Change from Baseline in respiratory rate variability 15 minutes after the intervention [15 minutes after the intervention]
To obtain the respiratory rate measurements, a respiratory belt transducer (Biopac Systems) was adjusted to the patient's thorax, at the xiphoid process level, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
- Change from Baseline in blood pressure variability immediately after the intervention [Immediately after the intervention.]
To obtain the blood pressure measurements, a digital sphygmomanometer was applied to the patient's left arm, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
- Change from Baseline in blood pressure variability 15 minutes after the intervention [15 minutes after the intervention.]
To obtain the blood pressure measurements, a digital sphygmomanometer was applied to the patient's left arm, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
- Change from Baseline in skin conductivity variability immediately after the intervention [Immediately after the intervention.]
To obtain the skin conductivity measurements, 2 electrodermal activity sensors (Biosignalsplux researcher) were connected to the patient's first finger, on the carpometacarpal and metacarpophalangeal joints, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
- Change from Baseline in skin conductivity variability 15 minutes after the intervention [15 minutes after the intervention.]
To obtain the skin conductivity measurements, 2 electrodermal activity sensors (Biosignalsplux researcher) were connected to the patient's first finger, on the carpometacarpal and metacarpophalangeal joints, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
- Change from Baseline in skin thermal variation immediately after the intervention [Immediately after the intervention.]
To obtain the skin thermal variation measurements, negative temperature coefficient (NTC) thermistor sensors (Biosignalsplux researcher) were connected to the patient's first finger, on the carpometacarpal and metacarpophalangeal joints, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
- Change from Baseline in skin thermal variation 15 minutes after the intervention [15 minutes after the intervention.]
To obtain the skin thermal variation measurements, negative temperature coefficient (NTC) thermistor sensors (Biosignalsplux researcher) were connected to the patient's first finger, on the carpometacarpal and metacarpophalangeal joints, with the patient lying supine. The sensor was only removed after completing all the evaluation moments.
Eligibility Criteria
Criteria
Inclusion Criteria:
- Healthy participants aged between 18 and 33 years.
Exclusion Criteria:
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Cognitive deficits that can possibly compromise the understanding of the study instructions;
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Any type of medication taken that may have influences at the variables under study in the previous 7 days;
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Cranio-cervical injuries, surgery to the skull and /or spine in the last 12 months;
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Chronic cardiorespiratory, renal, systemic, neurological, musculoskeletal, oncological and psychiatric pathologies;
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Headaches, migraines, dizziness and / or nausea while performing the techniques;
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Caffeine and / or alcohol intake in the 6 hours prior to the data collection;
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Tobacco consumption in the 30 minutes prior to the data collection;
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Practice of intense physical exercise in the 90 minutes prior to the data collection;
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Pregnant women or menstruating;
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Participants who were submitted to manual therapy treatments during the past month;
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Osteopathy students of 3rd year or higher degree, in order to prevent the participant from recognizing which group they belong to.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Escola Superior da Saúde do Porto | Porto | Portugal | 4200-072 |
Sponsors and Collaborators
- Escola Superior de Tecnologia da Saúde do Porto
Investigators
- Principal Investigator: Natália MO Campelo, Escola Superior de Saúde do Politécnico do Porto
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- OST1- 002