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Trial registered on ANZCTR
Registration number
ACTRN12607000497404
Ethics application status
Approved
Date submitted
24/09/2007
Date registered
28/09/2007
Date last updated
28/09/2007
Type of registration
Retrospectively registered
Titles & IDs
Public title
Evaluation of the effectiveness of Neuro Psycho Physical Optimization with Conveyer of Modulating Radiance (CMR) in stress-related physical and mental effort.
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Scientific title
A Randomised study to evaluate the effectiveness of Neuro Psycho Physical Optimization (NPPO) with Conveyer of Modulating Radiance (CMR Therapy) in reducing the subjective perception of stress, stress-related physical and mental effort.
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Stress, Stress-related physical and mental effort.
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Condition category
Condition code
Mental Health
2493
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0
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Other mental health disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The intervention comprises: A cycle of Neuro Psycho Physical Optimization (NPPO) with Conveyer of Modulating Radiance (CMR therapy). The CMR is a biomedical radiofrequency instrument. The protocol used, called Neuro Psycho Physical Optimization (ONPF), involves the application of a probe of the CMR on specific points of the auricular pavilion for an activation time of roughly 500 mms. The ONPF protocol is activated in a precise sequence on seven auricular points. The protocol envisages 18 sessions of ONPF treatment on alternating days, for eight (8)weeks. Assessment, at baseline and at the end of treatment, with Psychological Stress Measure Test (validated in Italian).
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Intervention code [1]
2115
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Treatment: Devices
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Comparator / control treatment
The reduction of the subjective perception of stress and stress-related physical and mental effort, after an NPPO cycle with CMR device, shows significant results (P<.05), respect to a control group that was treated with placebo (inactivated CMR) for the same period of 8 weeks.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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To test with Psychological Stress Measure if the use of the Conveyer of Modulating Radiance (CMR) - is effective in reducing the subjective perception of stress and stress-related physical and mental effort.
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Assessment method [1]
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Timepoint [1]
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At time zero and immediately after the cycle of therapy.
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Secondary outcome [1]
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Wellbeing - Neuro Psycho Physical Optimization.
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Assessment method [1]
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Timepoint [1]
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At time zero and immediately after the cycle of therapy.
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Eligibility
Key inclusion criteria
Subjects with any type of stress-related symptomatology, over 18 years old.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Subjects with psychiatric symptoms-pathologies, drugs dependence or aged less than 18 years of age were excluded.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
The subjects, concealed way, was allocated randomly to treatment or control group by an external operator.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation by an external operator - computerized sequence generation.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/01/2001
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
720
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Italy
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State/province [1]
604
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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Istituto Rinaldi Fontani
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Address [1]
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Via Nazionale 23 50123 Firenze
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Country [1]
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Italy
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Primary sponsor type
Charities/Societies/Foundations
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Name
Istituto Rinaldi Fontani
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Address
Via Nazionale 23 50123 Firenze
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Country
Italy
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Secondary sponsor category [1]
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Charities/Societies/Foundations
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Name [1]
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Societa di Ottimizzazione Neuro Psico Fisica e CRM Terapia
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Address [1]
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Via Nazionale 23 50123 Firenze
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Country [1]
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Italy
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Other collaborator category [1]
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University
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Name [1]
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University of Firenze - Department of Public Medicine - Occupational Health - Master of Second Level Ottimizzazione Neuro Psico Fisica e CRM Terapia
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Address [1]
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Largo Palagi 1 - 50139 Firenze
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Country [1]
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Italy
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Societa di Ottimizzazione Neuro Psico Fisica e CRM Terapia
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Ethics committee address [1]
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Via Nazionale 23 50123 Firenze
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Ethics committee country [1]
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Italy
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Date submitted for ethics approval [1]
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09/11/2000
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Approval date [1]
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09/11/2000
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Ethics approval number [1]
4561
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Summary
Brief summary
Physical and mental effort are the most frequent signs of general distress. In this study we have used the Psychological Stress Measure (validated in Italian) to test the effectiveness of Neuro Psycho Physical Optimization (NPPO) with Conveyer of Modulating Radiance - CMR Therapy in reducing the subjective perception of stress and stress-related physical and mental effort. The reduction of the symptomatology of stress and stress-related physical and mental effort after a NPPO cycle with CMR therapy shows significant results (P<.05) with respect to a control group that was treated with placebo (inactivated CMR).
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Vania Fontani M.D.
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Address
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Via Nazionale 23 50123 Firenze
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Country
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Italy
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Phone
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+39 055 290307
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Salvatore Rinaldi M.D
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Address
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Via Nazionale 23 50123 Firenze
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Country
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Italy
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Phone
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+39 055 290307
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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