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Active Vibration Induced Treatment by Abdominal Excitation

Active Vibration Induced Treatment by Abdominal Excitation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25538
Enrollment
60
Registered
2019-03-21
Start date
2019-04-15
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

chronic musculoskeletal pain disorders

Interventions

Each patient will have a schedule consisting of 3 weekly treatments over the course of 3 weeks. Each session will last 20 minutes and 27 seconds according to the length of the music. In all of the ei

Sponsors

University Medical Center Groningen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. The symptoms of pain have been present for 3 months or more 2. The symptoms of pain are present every day with a minimum level of NRS=4 (Moderate and severe pain) 3. The symptoms of pain are resulting from a condition diagnosed as a musculoskeletal disease listed in the ICD-10 of the WHO M00-M99.9 (But NOT M50.0, M50.1, M51.0 and M51.1 that are Prolapsus Disci Intervertebralis with myelopathy/radiculopathies – as the pain syndrome in these cases are expected to be predominantly neurogenic) 4. Adequate communication and understanding of the language 5. Age = 65 years 6. Available during the intervention.

Exclusion criteria

Exclusion criteria: 1. The medical examination showing signs of significant active, untreated comorbidities. Excluded are patients with Delirium and/or psychotic symptoms or moderate or severe depression. The distinction between light depression and moderate and severe depression is done according to the ICD-10: Light depression is F32.0 – moderate and severe depression are F32.1 and F32.2. 2. Patients with decreased signs of autonomic responses, metal implants such as ICD, organ transplantations and surgery on central nervous system in history. 3. The medical examination showing signs of the pain syndrome being exclusively or predominantly neurogenic with the condition diagnosed as a neurological disease listed in the WHO G00-G99.8. 4. The belt doesn’t fit properly. 5. Pain related to malignancies. 6. Enrolled in any other clinical study within the duration of the current study. 7. Enrolled in other music therapy. 8. Incapable of giving consent.

Design outcomes

Primary

MeasureTime frame
Numeric pain Ratomg Scale,Quality of Life (EuroQol - 5D 3L)

Secondary

MeasureTime frame
Pain disability index (PDI), Quantitative Sensory Testing (QST), Central sensitization index (CSI), Depression and Anxiety (HADS), Safety (UTAUT) and treatment satisfaction (ARTS)

Contacts

Public ContactT.F. Buisman

Universitair Medisch Centrum Groningen

t.f.buisman@umcg.nl050 3611464

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)