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Clinical Trials/NCT03363529
NCT03363529CompletedNot Applicable

ROOM-LIGHT: Dynamic LED-light as Treatment for Depressed Patients in Inpatient Wards: A Feasibility Trial

University Hospital Bispebjerg and Frederiksberg1 site in 1 country15 target enrollmentStarted: November 16, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
15
Locations
1
Primary Endpoint
Difference in numbers of drop out in the two groups

Study Overview

Brief Summary

Depression is a major health challenge, and despite developments in pharmacotherapy and psychotherapy a substantial part of patients will only recover very slowly and incompletely, and 10-25 % of the patients are resistant to treatment. Therefore, new treatment initiatives are in demand. Chronotherapeutics can regulate diurnal rhythms and sleep, and have shown promising results on antidepressant effects. Among chronotherapeutic treatment modalities, Bright Light Therapy (BLT) has been used in treatment of depression and sleep disorders for several decades with both an antidepressant and a sleep improving effect. BLT has also been shown to augment antidepressant therapy.

Objectives. The objective of this trial is to investigate the feasibility of a combination of LED-light armatures aiming to mimic sunlight, when installed in the patient rooms of a psychiatric inpatient Ward. Investigators has opted for using a randomized design that will subsequently be tested in a larger clinical trial with depression severity as the primary outcome. In this feasibility study investigators will register the stability of the system, the influence of the light on patients regarding tolerability, comfort, depression level, and sleep. Investigators also so want to measure and collect specific light-data on the Non-image-forming light (NIF) by using specially designed light sensors to capture the spectral distribution of the light. Finally investigators will test the electronic case report form (eCRF) that has been designed for the trial.

Design. The design is a randomised controlled feasibility trial with two arms: an active dynamic light trial arm and a standard light trial arm with blinding of depression outcome assessors (Hamilton depression rating scale), data collection, and data analyses. Randomization will be with a rate for active and standard of 2 to 1.

Detailed Description

Inclusion and exclusion criteria. Inclusion: Major depression disorder, age > 18 years, informed consent and Danish speaking.

Exclusion: Severe suicidality, actual psychotic state, bipolar disorder and if the patient is subject to coercive measures of any kind.

Name and description of experimental and control intervention. The experimental intervention is the implementation of a dynamic LED-light system in two patient rooms. The system includes three elements: a window jamb built-in light panel, two ceiling mounted lamps, and a wall mounted lamp. All lamps will have a dynamic, time dependent frequency distribution and intensity of light. The control intervention is constant standard LED-light with two elements: two ceiling mounted lamps and a wall mounted lamp.

Primary and secondary outcomes.

Primary outcome:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

Hamilton depression interview is done by external assessor blinded to condition

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Major depression disorder
  • Age > 18 years
  • Informed consent and Danish speaking.

Exclusion Criteria

  • Severe suicidality
  • Actual psychotic state
  • Bipolar disorder
  • Patient is subject to coercive measures of any kind.

Arms & Interventions

Standard

Placebo Comparator

This study arm utilizes a standard lighting condition in the patient room

Intervention: Standard (Device)

Dynamic

Experimental

This study arm utilizes a dynamic lighting from special designed lightfixtures in the ceiling and window sill.

Intervention: Dynamic light (Device)

Outcomes

Primary Outcomes

Difference in numbers of drop out in the two groups

Time Frame: Week 4

Number of patients in the two groups that drop out due to the standard or experimental lighting condition

Secondary Outcomes

  • Visual comfort questionaire(Week 4)
  • Change of depression level from baseline to endpoint(Change scores from baseline to week 4)

Investigators

Sponsor
University Hospital Bispebjerg and Frederiksberg
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Klaus Martiny

Professor of Clinical Psychiatry

University Hospital Bispebjerg and Frederiksberg

Study Sites (1)

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