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The reliability of event detection in parasomnia by the monitoring of heart rate changes.

The reliability of event detection in parasomnia by the monitoring of heart rate changes. - Parasomnia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30157
Enrollment
10
Registered
2006-08-24
Start date
2006-04-30
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

parasomnia sleep disorder

Interventions

None listed

Sponsors

Epilepsiecentrum Kempenhaeghe
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: between 18 and 60 years of age a body mass index between 18 and 30 suffering from NREM 3-4 and/or REM parasomnia minimal parasomnia frequency: 2 / week no acute behavioral problems, except as a part of RBD no acute intercurrent somatic disease that may interfere with study results informed consent form signed adult

Exclusion criteria

Exclusion criteria: epilepsy major or significant internal or neurological that interfere with teh measurements ESS score > 10/24 fast progressing neurological and / or systematic disorder pregnancy drugs or pacemakers that significantly influence hart rate inability to comply with the trial procedure inability to tolerate ECG electrodes presence of manifest psychiatric disorders below normal intelligence

Design outcomes

Primary

MeasureTime frame
Reliability, sensitivity and specificity of the detection of parasomnic events.

Secondary

MeasureTime frame
Comparison of event related detection with an one night polysomnography combined with videorecording; value of SCID and MMIP tests for the mental background of parasomnia.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)