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More or Less Pain with Muse

More or Less Pain with Muse - LLS-Pain

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42852
Enrollment
420
Registered
2016-08-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

geen aandoeningen: gezonde vrijwilligers, pijn en pijnverwerking Pain and painmodulation

Interventions

Music
Pain

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 18 years or older and they have knowledge of the Dutch language.

Exclusion criteria

Exclusion criteria: the use of painkillers in the last 12 hours, use of anti-depressants, pain in arm neck or shoulder (one or both sides), heart problems, neurological disorders, psychiatric disorders, wounds on hands or forearm, M. Raynaud, pregnancy, alcohol percentage of > 220 UGL.

Design outcomes

Primary

MeasureTime frame
Main study parameters/endpoints: Pressure tolerance will be measured via algometry (Wagner force, USA) on five places on the dorsal side of the non dominant forearm and expressed in Newton (N). Electrical pain tolerance thresholds are assessed on two places on the dorsal side of the nondominant forearm and expressed in milliAmpere (mA). Duration in the icewaterbucket (IWB) with the dominant hand will be recorded in seconds (s) with a maximum of three minutes (180s). After the IWB test the pressure tolerance or the electrical pain tolerance thresholds will be recorded again. Conditioned pain modulation (CPM) will be calculated by use of the formula ((pressure post-pressure pre)/pressure pre)*100 expressing the precentage of painmodulation.

Secondary

MeasureTime frame
Secondary endpoints are the sensitivity for pain (assessed with the Pain Sensitivity Questionnaire (PSQ), amount and quality of sleep (Pittsburg Sleep Quality Index) and the Quality of Life (assessed with the EQ-5D).In addition, the subject will be asked after the completion of the investigation how burdensome they found the measurements.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)