Clinical Trials in the Netherlands / NCT06215235
Recruiting Observational

Implementation of Bright Light Therapy ID

NCT06215235 · tracked via the Priya Life Science Netherlands tracker
Phase
Observational
Started
2023-10-18
Last updated
2025-09-25

Condition(s) studied

Depressive Symptoms

Investigational drug(s) / intervention(s)

Bright light therapy

Bright light therapy: for 2 weeks the patient will take place for a 10.000lux lamp for 20-30 minutes.

Study summary

Many adults with intellectual disabilities (ID) have depressive symptoms, which negatively impact their quality of life. A lot of of the non-medicinal forms of treatment are not or hardly suitable for people with ID. Bright light therapy (BLT) seems to be a good option. Earlier research has shown that BLT is applicable in this group and seems promising in terms of reducing depressive symptoms, without serious side effects.

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Involved in the implementation of BLT (staff) OR * 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: * n/a

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
ErasmusMC Rotterdam Netherlands Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06215235 on ClinicalTrials.gov ↗ ← All trials in the Netherlands