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BioClock: Bright Light Therapy for Depressive Disorders

Not Applicable
Recruiting
Conditions
Depression, Unipolar
Depression, Bipolar
Interventions
Procedure: Bright Light Therapy
Device: Blue Light Blocking Glasses
Registration Number
NCT05958940
Lead Sponsor
Universiteit Leiden
Brief Summary

Bright Light Therapy (BLT) is a proven treatment for depression in seasonal and non-seasonal depressive disorders, as well as bipolar disorder. To make BLT more effective and practical in clinical settings and tailor it to individual needs, it is necessary to optimize the treatment approach, understand how the treatment works, and identify patient characteristics that predict response.

This clinical trial has three main goals:

* Optimize the administration of BLT for patients with depressive episodes.

* Gain a deeper understanding of the treatment mechanisms.

* Determine which patients benefit the most from the treatment.

The specific objectives are as follows:

* Investigate whether additional treatments and interventions related to lifestyle and the biological clock can enhance the effects of BLT.

* Examine how BLT influences the body's internal clock and sleep quality, and how these factors contribute to the outcomes.

* Identify patient characteristics and behaviours that can predict treatment outcomes.

* Develop a brain model to better understand the impact of BLT on the brain.

In this study, patients will receive BLT with a light intensity of 10,000 lux for 30 minutes each morning over 5 consecutive days. The treatment duration will range from one to three weeks, depending on the improvement of depressive symptoms. Participants will be randomly assigned to one of three groups:

* Home - Patients will receive BLT at home, following the standard guidelines for light therapy in the Netherlands.

* LightCafé, fixed time: Patients will receive BLT in a café-like setting called the LightCafé, where the focus is not only on symptom improvement but also lifestyle enhancements and fostering social connections. The treatment time will be the same every day.

* LightCafé, varying time: Patients will also receive BLT at the LightCafé, with treatment timing varying each day. Additionally, this group will wear glasses in the evening that filter blue light.

The study includes a baseline phase of up to two weeks, a treatment phase of up to three weeks, and a three-month follow-up phase. Patients will wear a motion watch to assess sleep-wake behaviour and physical activity during the day. Additionally, they will wear a broach that measures their personal light exposure throughout the day. Eight one-minute questionnaires per day will be sent to the participants' smartphones to assess vitality, sleep, and mood during the treatment. Predictors of treatment response, such as clinical characteristics, sleep measures, circadian parameters, and light-related behaviours, will be evaluated at baseline. In a small group of patients, salivary melatonin curves will be assessed before and after treatment. MRI scans will provide insights into functional and structural brain changes following light therapy treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
231
Inclusion Criteria
  • Age between 18 and 65.
  • Diagnosis of unipolar or bipolar depression (seasonal or non-seasonal) as assessed with the Mini-International Neuropsychiatric Interview (M.I.N.I.)
  • A current depressive episode (a score of 6 or higher on the Quick Inventory of depressive symptomatology Self Report (QIDS-SR)
  • Sufficient knowledge of Dutch or English language to fill in questionnaires
  • Provided Informed consent
Exclusion Criteria
  • A current (hypo)manic or mixed episode (as assessed with the M.I.N.I.)
  • Current psychotic episode (as assessed with the M.I.N.I.)
  • Prominent active suicidality (score 10 or higher on the M.I.N.I. module)
  • Antidepressant therapy (medication, psychotherapy or BLT, or other forms of specific treatments for depression) that started less than 2 months prior to study entry
  • participants with bipolar disorder should be in mood-stabilizing treatment for at least 1 month in a recommended dosage,
  • Use of melatonin or agomelatine in the last month
  • Current use of antibiotics
  • Current use of light sensitivity increasing medication
  • Travelled across more than 1 time zone during past month or during the treatment
  • Travelled to sunny holiday locations/winter sports during past month
  • pre-existing eye and skin disorders (retinitis pigmentosa, porphyria, chronic actinic dermatitis and sun-induced urticaria)
  • Systemic disorders with potential retinal involvement (rheumatoid arthritis and systemic lupus erythematosus)
  • Suffering from colour blindness (assessed by Ishihara colour plates)
  • Participated in night shift work in the last three months
  • (Retinal) blindness, severe cataract and glaucoma
  • Light-induced migraine or epilepsy
  • Pregnancy, or parents with a child younger than 18 months old

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
LightCaféBright Light TherapyBLT will be administered in a specialized cafe, under the supervision of clinical staff, promoting lifestyle changes and social interaction.
LightCafé+Bright Light TherapyTreatment will be identical to the second arm but now complemented with the use of blue-light blocking glasses in the evening and the adoption of personalized BLT timing based on sleep-wake patterns
LightCafé+Blue Light Blocking GlassesTreatment will be identical to the second arm but now complemented with the use of blue-light blocking glasses in the evening and the adoption of personalized BLT timing based on sleep-wake patterns
Light@HomeBright Light TherapyStandard Care - BLT in the home environment
Primary Outcome Measures
NameTimeMethod
Clinical Improvement2-5 weeks

Difference between pre- and post-treatment assessment of the Montgomery Asberg Depression Rating Scale \[MADRS\]

Secondary Outcome Measures
NameTimeMethod
Remission rates, self assessed and clinician rated2-5 weeks for clinician rated. Up until 4 months after start treatment for self-assessed

percentage of patients that after treatment have a score of \<6 on the MADRS or QIDS-SR

Circadian Periodicity2-5 weeks

Changes in circadian periodicity will be compared between groups. Circadian periodicity is a period of an oscillating rhythm assessed via periodogram analysis of the activity time-course of actigraphy data. The deviation between the maximum period of the periodogram and the normal daily period of 24h reflects pattern variability in normal entrainment conditions.

Intra-daily variability2-5 weeks

rhythm fragmentation

Chronotype1-3 months

Chronotype changes as assessed with the Morningness-Eveningness Questionnaire(MEQ) and the Ultra-Short Version of the Munich Chronotype Questionnaire (µMCTQ)

Subjective change in depressive symptom severityfrom baseline until follow-up, approximately 4 months

Change in score on the Quick Inventory of Depressive Symptoms, Self Report (QIDS-SR)

Time to remissionone, two or three weeks

The time it takes to achieve remission, if remission is achieved. Measured with QIDS-SR

Circadian amplitude2-5 weeks

Changes in the circadian amplitude will be compared between groups. The amplitude can be estimated from actigraphy data by the difference in activity between the most active 10h and the least active 5h normalized for total activity.

Circadian phase2-5 weeks

Changes in circadian phase will be compared between groups as assessed using the DLMO (calculated from the melatonin assessments) and complemented with actigraphy data (using sleep onset timing, least active 5h period and most active 10h period)

Sleep-Wake Pattern2-5 weeks

Actigraphy and questions from The Consensus Sleep Diary will provide sleep onset time, sleep offset time, midsleep time, total sleep time, sleep onset latency, number of awakenings and time awake during the night.

Sleep Quality2-5 weeks for actigraphy, up until 4 months after the start of treatment for subjective sleep quality

Fragmentation index (degree of movement during the night), sleep efficiency (total sleep time expressed as a percentage of time in bed) will be calculated using actigraphy data. The Pittsburgh Sleep Quality Index (PSQI) will provide a subjective measure of sleep quality.

Response Rates, self assessed and clinician rated2-5 weeks for clinician rated, Up until 4 months after start treatment for self-assessed

percentage of patients hat after treatment have at least 50% reduction in depressive symptom, measured using MADRS and QIDS-SR

Inter-daily stability2-5 weeks

Constancy of the 24-h rhythmic pattern over days

Severity of Insomnia Symptomsup until 4 months after the starts of treatment

Severity of Insomnia Symptoms as assessed with the Insomnia Severity Index

Gray matter structure2-5 weeks

Properties of gray matter structure (thickness, volume, surface area and gyrification) of the whole brain as well as of the white matter structure (integrity of main white matter fiber tracts-fractional anisotropy (FA))

Functional connectivity of the brain2-5 weeks

Functional connectivity of the brain under resting state condition - the communication of specific brain regions which work as a network without conducting a specific task

Momentary Positive/Negative Affect2-5 weeks

The EMA will consist of items from the Positive and Negative Affect Scale (PANAS) to assess momentary positive and negative affect

Momentary Vitality2-5 weeks

The EMA will contain 4 items concerning energy levels and alertness adapted from Activation-Deactivation Adjective Checklist

Trial Locations

Locations (2)

GGzE - Mental Health Institute of Eindhoven and the Kempen

🇳🇱

Eindhoven, Netherlands

Leids Universitair Behandel- en Expertise Centrum

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Leiden, Netherlands

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