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Daylight during Recovery of Depression

Daylight during Recovery of Depression - DaR (Daylight and Recovery)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57455
Enrollment
30
Registered
2024-10-27
Start date
2026-04-23
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

clinical depression in remission Major Depressive Disorder (MDD) in remission Remission after depression

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) A past year diagnosis of a unipolar major depressive disorder according to DSM-5 criteria, 2) Full or partial remission, i.e. not meeting the DSM-5 criteria for a depressive episode within the past two months, 3) Age 20 years or older.

Exclusion criteria

Exclusion criteria: 1) Eye conditions affecting light transmittance to the retina, 2) An established or suspected diagnosis of a major neurocognitive disorder, 3) A severe mental illness, defined as a bipolar or primary psychotic disorder or a severe substance-use disorder in need of treatment, 4) Seasonal affective disorder, 5) Not able to fill out self-report questionnaires, 6) Shift work. 7) Regular usage of melatonin, within 3 weeks prior to the start of the measuring period. 8) Receiving light treatment

Design outcomes

Primary

MeasureTime frame
The main outcomes are positive and negative affect, operationalized as momentary positive (PA) and negative affect (NA) based on the circumplex model of affect. The main determinant is time spent in (day)light, assessed with a question in the diary in three time intervals per day (morning, afternoon, and evening), and assessed objectively with the light sensor as time spent in >1000 lux. We will assess which operationalization is the strongest predictor of affect.

Secondary

MeasureTime frame
General covariables used for every research question are physical activity, social interactions, exposure to green environments, use of medication and important events, which will be asked in the diary. Age, sex and education level, chronotype, depressive symptom severity and presence of sleep disturbances will be assessed during the baseline interview with questionnaires. The phase of the circadian pacemaker will be evaluated with dim light melatonin onset assessment at the end of the 30-day study period. Sleep will be assessed with actigraphy. For circadian rhythms, we will assess the interdaily stability, intradaily variability, and relative amplitude.

Countries

Netherlands

Contacts

Public ContactM Zuidersma

Universitair Medisch Centrum Groningen

m.zuidersma@umcg.nl06-86558458

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: May 16, 2026