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*GESOND' - testing for electromagnetic sensibility*

*GESOND' - testing for electromagnetic sensibility* - *GESOND'

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON40434
Enrollment
40
Registered
2014-07-23
Start date
2014-09-02
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

electrogevoeligheid electromagnetic sensibility

Interventions

Participants can choose which signal they want to get tested from an array of selectable signals, such as DECT phone, WiFi or base station signals, or extremely-low frequency fields, such as a LED l

Sponsors

Universiteit Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: The study population for the experiment will consist of up to 40 adult subjects reporting electromagnetic sensibility. Adult participants (older than 18 years old), with sufficient profiency in Dutch language, will be included if they report electromagnetic sensibility, i.e. the ability to sense one of the available experimental (real-life) EMF signals within minutes of being exposed, or developing acute and transient health complaints that occur and disappear within 15 minutes if exposure is short.

Exclusion criteria

Exclusion criteria: Inability to complete the administered questionnaires, e.g. due to insufficient knowledge of the Dutch language or cognitive impairment. Time between start of exposure and sensing exposure or development of symptoms plus recovery time from symptoms exceeds 15 minutes.

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study will be the difference in self-rated electromagnetic sensibility as measured on a 100 mm visual analogue scale comparing the rating at 2 months after testing in the immediate testing arm with the scoring prior to testing in the delayed testing arm.

Secondary

MeasureTime frame
The secondary outcomes will be (a) the frequency of persons able to by repetition correctly assess whether exposure is present or absent in the double-blind testing, and (b) the longitudinal course of self-rated electromagnetic sensibility in the subsequent questionnaires (baseline, directly pre/post-testing at home visit and follow-up after home visit), as measured on a 100 mm visual analogue scale.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)