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Pilot study of the feasibility of research on the application of bright light as a means of restoring the sleep-wake rhythm in patients with schizophrenia admitted to the locked ward, and by that means alleviating their psychotic symptoms.

Pilot study of the feasibility of research on the application of bright light as a means of restoring the sleep-wake rhythm in patients with schizophrenia admitted to the locked ward, and by that means alleviating their psychotic symptoms. - Light Therapy in Schizophrenia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON33052
Enrollment
20
Registered
2009-09-04
Start date
2009-09-10
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

disturbed circadian rhythm in schizophrenia

Interventions

Intervention: The intervention group will receive treatment as usual plus daily exposure to bright white light (5.000 lux) for the duration of 5 days, in the morning between 8 and 9 o*clock, for hal

Sponsors

Parnassia (Den Haag)
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - All patients diagnosed with schizophrenia or schizoaffective disorder by a psychiatrist according to the DSM-IV TR classification. - Patients who are admitted to the clinical institution KCVG. - Patients for whom informed consent and informed consent by proxy has been given.

Exclusion criteria

Exclusion criteria: - Patients with diagnosis of bipolar disorder. - Patients with a current manic episode measured with the Young Mania Rating Scale. - Patients with contra-indications for light therapy after eye examination, such as glaucoma, retinopathy or cataracts. - Patients with epilepsy in history or at present

Design outcomes

Primary

MeasureTime frame
The main study parameter is the change from baseline to endpoint in level of psychosis measured with the PANSS.

Secondary

MeasureTime frame
The secondary study parameter is the change in the sleep-wake rhythm and activities measured with a sleep log and a social rhythm therapy scheme.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)