Bright Light Therapy in the Treatment of Non-seasonal Bipolar Depression

Phase 1

• Conditions: Bipolar Depression
• Interventions: Device: Light

• Registration Number: NCT03396744
• Lead Sponsor: Assistance Publique - Hôpitaux de Paris

Brief Summary

Bipolar disorder (BD) is a severe brain disorder characterized by the recurrence of mood episodes. Depressive episodes in BD are frequently refractory and clinicians have few treatment options. Bright light therapy (BLT, also named phototherapy) is a promising emerging antidepressant strategy that is lacking evidence-based guidelines for its prescription in BD, including to avoid side effects such as manic switches. In this context, this study aimed to evaluate modalities of the BLT dosage (time of exposure) escalation depending on the tolerance (manic symptoms) in two groups exposed either during the morning or at mid-day.

Detailed Description

Bipolar disorder (BD) is a severe brain disorder characterized by the recurrence of mood episodes. Patients presenting with BD spend more time with depressive symptoms than with manic ones, which have a major impact on the quality of life and is associated with poorer outcomes including recurrences and suicide. In addition depressive phases in BD are frequently refractory and clinicians have few treatment options. Bright light therapy (BLT, also named phototherapy) is the first line treatment for depression with seasonal patterns and show promising results in the treatment of non-seasonal depressions. More evidence in non-seasonal depressions is expected, especially in BD. Moreover, some specificities linked to BD, such as the manic switch, warrant evidence-based therapeutic guidelines and so deserve more studies in BD. Preliminary reports suggest that morning exposure may induce manic switches, and that mid-day exposures may be associated with a decreased risk of manic switch. Different dose-titration protocols have also not been compared, and data are lacking. In this context, this study aimed to evaluate modalities of the BLT dosage (time of exposure) escalation depending on the tolerance (manic symptoms) in two groups exposed either during the morning or at mid-day.

Study Timeline

• Study First Submitted: 2018-01-02
• Study First Submitted QC: 2018-01-10
• Study First Posted: 2018-01-11
• Study Start: 2019-09-30
• Status Verified: 2020-02
• Last Update Submitted: 2020-02-07
• Last Update Posted: 2020-02-10
• Primary Completion: 2020-07
• Study Completion: 2021-01

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

• Patients must be aged from 18 to 55 year-old.
• Patients must read and understand French language, and must provide written informed consent.
• Patients must be inpatients or outpatients followed in psychiatry for a major depressive episodes.
• Patients must have a diagnosis of bipolar disorder, type I or II, according to the DSM-5 and determined by a SCID.
• Patients must have a major depressive episode, at least of moderate intensity, according to the DSM-5, with a MADRS total score ≥20 and determined by a SCID.
• Patients must have a mood stabilizer since at least 4 weeks at standard dosage (lithium, or sodium valproate, or second generation antipsychotics such as quetiapine, aripiprazole, olanzapine).
• Female patients must be using a medically accepted means of contraception.
• Patients must be affiliated to the social security scheme.

Exclusion Criteria

• Patients under guardianship or deprivation of liberty by administrative or judicial decision

• Seasonal pattern of major depressive episode according to DSM-5 criteria.

• Psychotic, mixed, or catatonic characteristics according to DSM-5 criteria

• High suicidal risk assessed by the Columbia Scale of Suicide Risk Severity (C-SSRS)

• Not stabilized comorbidities (addictive disorders according to the DSM-5 criteria or other decompensated general medical cause).

• Ophthalmic pathology (cataract, macular degeneration, glaucoma, retinitis pigmentosa) and diseases affecting the retina (retinopathy, diabetes, herpes, etc.).

• Photosensitive treatment, including the following treatments:

  • Cyclins (Vibramycin®, Doxycycline®)
  • Amiodarone (Cordarone®, Amiodarone®)
  • Phenothiazines (Largactil®, Modecate®, Nozinan®, Melleril®, Trilafon®)
  • Methotrexate (Methotrexate®)
  • Sulfamides (antibiotics, diuretics or hypoglycemic agents)
  • Chloroquine (Nivaquine®)
  • Some anti-inflammatories (Apranax®, Indocid®)
  • Psoralens used in puvatherapy
  • Isotretinoin (Roaccutane® and generics)
  • Verteporfin (Visudyne®).

• Lactating or pregnant women (pregnancy urine positive test).

• Subjects who have already used light therapy in the last 6 months.

• Therapeutic resistance of the current major depressive episode (≥2 traditional antidepressants such as SSRI, IRSNA, MAOI or tricyclic, at effective therapeutic dosage for more than 6 weeks)

• Use of another antidepressant strategy than the mood stabilizer, including antidepressants of all classes (which will have to be stopped before the initiation of light therapy) and psychotherapy with onset <1 month.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Morning group	Light	Exposition at 8 a.m +/- 30 min, during 10 active weeks, and assessed 6 months after this intervention
Mid-day group	Light	Exposition at 8 a.m +/- 30 min, during 10 active weeks, and assessed 6 months after this intervention.

Primary Outcome Measures

Name	Time	Method
Change in Mania Score	10 weeks	The Young Mania Rating Scale (YMRS) will be used as a measure of tolerance reflecting change in YMRS total scores at each week over the 10 weeks (Total score ≥ 12 defining an hypomanic switch).

Secondary Outcome Measures

Name	Time	Method
Change in Depression Score	6, 8 and 10 weeks	The Montgomery-Asberg Depression Rating Scale (MADRS) will be used as a measure of efficacy reflecting changes from baseline to endpoint
Acceptability	1, 2, 3, 4, 5, 6, 8 and 10 weeks	measured by auto-questionnaire made by the investigators
Change in Clinical Global Impressions (CGI)	6, 8 and 10 weeks	The Clinical Global Impressions (CGI) will be used as a measure of efficacy reflecting changes from baseline to endpoint
Change in tolerance	1, 2, 3, 4, 5, 6, 8 and 10 weeks	YMRS will be used to evaluate hypomanic switch at 3 days after each duration of exposition change
MADRS	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then at 6 months	The MADRS will be used to evaluate changes of depressive symptoms from baseline
Quick Inventory of Depressive Symptomatology (QIDS SR-16)	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months
Altman Self-Rating Mania Scale (ASRM).	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months
Circadian Type Inventory (CTI).	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months
Epworth Sleepiness Scale (ESS).	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months
Clinical Global Impressions (CGI).	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months
Columbia-Suicide Severity Rating Scale (C-SSRS)	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months
Pittsburgh Sleep Quality Index (PSQI).	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months
Side effects: PRISE-M	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months
Composite Scale of Morningness (CSM).	1, 2, 3, 4, 5, 6, 8 and 10 weeks, and then 6 months

Trial Locations

Locations (1)

Fenand Widal hospital; 🇫🇷 Paris, France