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Light to fight addiction

A placebo-controlled trial to test the effectiveness of a lighting intervention to reduce or stabilize alcohol use and craving in alcohol dependent patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON24477
Enrollment
60
Registered
2018-10-26
Start date
2018-12-01
Completion date
Unknown
Last updated
2024-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic alcohol dependency

Interventions

One group (intervention group) will receive behavioural instructions (about sleep-wake timing) combined with a lighting intervention aimed to facilitate adherence to these instructions and to increase

Sponsors

Technische Universiteit Eindhoven
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: Patients should be under current, active treatment of the FACT team, with primary alcohol dependence, capable of adherence to agreements with FACT team (based on a maximum of 30% of not showing up for meetings at the clinic or being at home for home visits by caregiver), and are aged 24-65 years old. Moreover, they should be fluent in the Dutch language.

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: • Current florid psychosis • Depression, prominent suicidal and/or homicidal ideation with active intervention during the month prior to the moment of investigation and expected active intervention during the actual research period • Mentally incompetent • Homelessness, or a housing condition that impedes participation • Relatively high use of (pre-scribed) sleep mediation as reported by caregiver or use of illegal sleep medication • Two or more time zones trans-meridian flights one month prior to participation • Shift work during the three months prior to participation • Color blindness assessed with Ishihara test • Visually impaired • Recent eye surgery (last year), glaucoma or other eye disease

Design outcomes

Primary

MeasureTime frame
The main study parameters are self-reported number of drinking days, number of alcoholic drinks consumed and alcohol craving

Secondary

MeasureTime frame
Sleep timing, duration, and quality, degree of circadian (mis)alignment, self-control with respect to resisting alcohol, vitality, mood, quality of life, and adherence to behavioral instructions

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)