search
Back to results

ROOM-LIGHT: Dynamic LED-light as Treatment for Depressed Patients in Inpatient Wards (ROOM-LIGHT)

Primary Purpose

Depression, Light; Therapy, Complications, Sleep Disorders, Circadian Rhythm

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Dynamic light
Standard
Sponsored by
Mental Health Centre Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring Dynamic lighting, ipRGC

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Mental Health Centre CopenhagenRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Standard

Dynamic

Arm Description

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

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

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Visual comfort questionaire
Difference in scores in the Visual comfort questionaire
Change of depression level from baseline to endpoint
Difference in change scores on the Hamilton Depression Rating scale 17 item from baseline to week 4 in the two groups

Full Information

First Posted
November 16, 2017
Last Updated
December 5, 2017
Sponsor
Mental Health Centre Copenhagen
Collaborators
Copenhagen Trial Unit, Center for Clinical Intervention Research, Chromaviso A/S, Department of Photonics Engineering
search

1. Study Identification

Unique Protocol Identification Number
NCT03363529
Brief Title
ROOM-LIGHT: Dynamic LED-light as Treatment for Depressed Patients in Inpatient Wards
Acronym
ROOM-LIGHT
Official Title
ROOM-LIGHT: Dynamic LED-light as Treatment for Depressed Patients in Inpatient Wards: A Feasibility Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 16, 2017 (Actual)
Primary Completion Date
July 15, 2018 (Anticipated)
Study Completion Date
December 15, 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mental Health Centre Copenhagen
Collaborators
Copenhagen Trial Unit, Center for Clinical Intervention Research, Chromaviso A/S, Department of Photonics Engineering

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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: 1. Rate of patients discontinuing the trial due to discomfort from the lighting condition. Secondary outcomes: Mean scores on the visual comfort scale in the intervention period Reduction in HAM-D17 scores from baseline to week 4 Trial size. In total 15 patients. All regulatory approvals has been met from the Danish Data Protection Agency, the regional Ethics Committee Agency, and the Mental Health Services of Copenhagen. Time schedule. The first participant is expected to be enrolled in December 2017. The expected last follow-up of the last participant will be June 2018. Data will be analysed from June 2018 till December 2018. Manuscripts will be prepared from June 2017 and we expect to submit first manuscript January 2019.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Light; Therapy, Complications, Sleep Disorders, Circadian Rhythm
Keywords
Dynamic lighting, ipRGC

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Standard versus dynamic lighting
Masking
Outcomes Assessor
Masking Description
Hamilton depression interview is done by external assessor blinded to condition
Allocation
Randomized
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard
Arm Type
Placebo Comparator
Arm Description
This study arm utilizes a standard lighting condition in the patient room
Arm Title
Dynamic
Arm Type
Experimental
Arm Description
This study arm utilizes a dynamic lighting from special designed lightfixtures in the ceiling and window sill.
Intervention Type
Device
Intervention Name(s)
Dynamic light
Intervention Description
Dynamic lighting is light that changes in intensity and spectral distribution during the day
Intervention Type
Device
Intervention Name(s)
Standard
Intervention Description
Standard lighting is non-dynamical light corresponding to standard hospital lighting.
Primary Outcome Measure Information:
Title
Difference in numbers of drop out in the two groups
Description
Number of patients in the two groups that drop out due to the standard or experimental lighting condition
Time Frame
Week 4
Secondary Outcome Measure Information:
Title
Visual comfort questionaire
Description
Difference in scores in the Visual comfort questionaire
Time Frame
Week 4
Title
Change of depression level from baseline to endpoint
Description
Difference in change scores on the Hamilton Depression Rating scale 17 item from baseline to week 4 in the two groups
Time Frame
Change scores from baseline to week 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Klaus Martiny, DMSc, PhD
Phone
0045-38647100
Email
klaus.martiny@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Signe Dunker Svendsen, Nurse
Phone
0045-38647102
Email
signe.dunker.svendsen@regionh.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Klaus Martiny, DMSc, PhD
Organizational Affiliation
Mental Health Centre Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mental Health Centre Copenhagen
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Klaus Martiny, DMsc
Phone
0045-38647100
Email
klaus.martiny@regionh.dk

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31956421
Citation
Volf C, Aggestrup AS, Svendsen SD, Hansen TS, Petersen PM, Dam-Hansen C, Knorr U, Petersen EE, Engstrom J, Hageman I, Jakobsen JC, Martiny K. Dynamic LED light versus static LED light for depressed inpatients: results from a randomized feasibility trial. Pilot Feasibility Stud. 2020 Jan 15;6:5. doi: 10.1186/s40814-019-0548-9. eCollection 2020.
Results Reference
derived

Learn more about this trial

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

We'll reach out to this number within 24 hrs