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Evaluation of the effectiveness of Neuro Psycho Physical Optimization with Conveyer of Modulating Radiance (CMR) in patients with stress-related pains and physical problems.

A Randomised controlled trial to evaluate 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 pains and physical problems

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12607000456459
Acronym
CRMTP
Enrollment
900
Registered
2007-09-11
Start date
2001-01-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

It has been shown a relationship between chronic widespread pain and visceral sensations of pain and psychological distress. Chronic stress causes a progressive malfunction in some structures of the nervous system which contribute to generating the symptoms of stress correlated pains and physical problems. In this study we have use the Psychological Stress Measure Test (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, pains and physical problems stress-related.

Interventions

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).

Sponsors

Istituto Rinaldi Fontani
Lead SponsorCharities/Societies/Foundations

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to -2147483648 No limit
Healthy volunteers
No

Inclusion criteria

Subjects with Psychological Stress Measure Test positive for Pains and physical problems.

Exclusion criteria

Subjects taking major analgesic or suffering from organic or neoplastic pain or aged less than 18 years of age were excluded.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026