Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06781593

Combining Light Therapy and CPAP in Depression

Led by Hôpital le Vinatier · Updated on 2025-04-29

130

Participants Needed

2

Research Sites

145 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In a double-blind, parallel-group controlled trial, we aim to measure the effect of two weeks of light therapy combined with the CPAP on compliance CPAP in patients with major depressive disorder.

CONDITIONS

Official Title

Combining Light Therapy and CPAP in Depression

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults consulting at the MICHEL JOUVET unit, CH Le Vinatier, Bron
  • Diagnosis of major depressive episode (DSM-V) with MADRS score ≥ 15
  • Diagnosis of obstructive sleep apnea syndrome (OSAS) by ventilatory polygraphy or polysomnography (AASM 2017 criteria) requiring CPAP treatment
Not Eligible

You will not qualify if you...

  • Refusal to participate
  • Pregnant or breastfeeding women
  • Under guardianship or curatorship
  • Unstable psychiatric or physical conditions such as hypomania or high suicidal risk deemed incompatible with the study
  • Other psychiatric, neurological, or somatic disorders
  • Contraindications to light therapy, including retinopathy, retinitis pigmentosa, diabetic retinopathy, macular degeneration, glaucoma, or eye surgery within the past 3 months
  • Choosing a provider other than the protocol's designated provider
  • Choosing devices other than SEFAM's S-BOX or a nasal mask at CPAP introduction
  • Nasal obstruction
  • Refusal to use actimetry, light therapy, or CPAP

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Centre Hospitalier le Vinatier

Bron, France, France, 69678

Actively Recruiting

2

Centre Hospitalier le Vinatier

Bron, France, 69678

Not Yet Recruiting

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Research Team

S

Sébastien S CATOIRE, Dr

CONTACT

L

Lydie L SARTELET, Mrs

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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