Skip to content

Effect of a Single Nights' Wake Followed by Bright Light Therapy for Severe Depression

Wake and Bright Light Therapy for Depression Among Admitted Patients

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02503124
Enrollment
32
Registered
2015-07-20
Start date
2015-07-31
Completion date
2020-03-15
Last updated
2021-04-02

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

Conditions

Depression

Brief summary

A randomized controlled trial comparing wake therapy (single night) followed by bright light therapy to treatment as usual.

Interventions

BEHAVIORALSingle night's wake therapy

Eligible patients are assisted in maintaining total sleep deprivation during one night

Bright light according to patients´ own circadian rhythm each morning for a week.

OTHERTreatment as usual - inpatient care

All patients are admitted due to severe depression and are under observation and most receive antidepressive medication and if necessary anxiolytic/antipsychotic medication.

OTHERInformative meeting

A short sleep hygiene consultation.

DRUGTreatment as usual - medicine

Since all patients are admitted due to a severe mental illness, they will receive medication according to indication. Most patients have already tried more than one antidepressant at the time of admission. In cases of severe anxiety, anxiolytics are prescribed but this is kept to a minimum.

Sponsors

Sahlgrenska University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Depressive episode requiring admission to a psychiatric hospital (including unipolar and bipolar depression).

Exclusion criteria

* Psychotic symptoms/agitation * Compulsory admission * Confusion * Active substance use disorder * Eye disease preventing bright light therapy

Design outcomes

Primary

MeasureTime frameDescription
MADRS-S score reduction of 50%One weekMontgomery Asberg Depression Rating Scale

Secondary

MeasureTime frameDescription
Re-admission10-14 weeks
CGI scoreOne weekClinical global impression
MADRS-S score at dischargeParticipants will be followed at discharge, an expected average of 2-3 weeksMontgomery Asberg Depression Rating Scale
MADRS-S score at follow-up10-14 weeksMontgomery Asberg Depression Rating Scale
Length of stayThe number of days between admission and dischargePatients will be followed up 10-14 weeks after discharge and the total number of days in inpatient services calculated.
ISI score score at follow-up10-14 weeksInsomnia Severity Index - Self administered scale of sleep quality
ISI score reduction of 50%One weekInsomnia Severity Index - Self administered scale of sleep quality
Medication use10-14 weeksThe use of antidepressants, anxiolytics or other psychiatric medication will be registered at follow-up. The number of patients using more than one medication and the dosage will be compared.
ISI score score at dischargeParticipants will be followed at discharge, an expected average of 2-3 weeksInsomnia Severity Index - Self administered scale of sleep quality

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026