Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
105 participants
OBSERVATIONAL
2023-10-18
2026-05-31
Brief Summary
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In part 1 of this project we investigate the implementation of BLT at Amarant. We will take the lessons learned into part 2 of this project: the implementation of BLT at Abrona. We will evaluate this process and the outcomes.
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
OTHER
Study Groups
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Persons involved in BLT
Persons with ID and staff who are involved in BLT. Either by receiving BLT, or by prescribing or facitating BLT.
Bright light therapy
for 2 weeks the patient will take place for a 10.000lux lamp for 20-30 minutes.
Interventions
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Bright light therapy
for 2 weeks the patient will take place for a 10.000lux lamp for 20-30 minutes.
Eligibility Criteria
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Inclusion Criteria
* Involved in the prescription or application of BLT (staff/relatives) OR
* receiving BLT for their depressive symptoms (patients with ID)
* 18 years or older
* informed consent
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Erasmus Medical Center
OTHER
Responsible Party
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Margreet Vlastuin
Research Coordinator Quality
Locations
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ErasmusMC
Rotterdam, , Netherlands
Countries
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Facility Contacts
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Other Identifiers
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Wouters
Identifier Type: OTHER
Identifier Source: secondary_id
Panama-10390
Identifier Type: -
Identifier Source: org_study_id
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