Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06781593

Effects of Light Therapy on Compliance With Continuous Positive Airway Pressure in Patients With Major Depression and Obstructive Sleep Apnea

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

130

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the impact of combining two weeks of light therapy with continuous positive airway pressure (CPAP) treatment on CPAP compliance in patients who have both major depressive disorder (MDD) and obstructive sleep apnea syndrome (OSAS). MDD is a common and disabling condition characterized by persistent depressed mood, loss of interest, and sleep disturbances. Since sleep problems and depressive symptoms are linked, treating sleep disorders like OSAS may improve depression outcomes. This study aims to see if adding light therapy to CPAP improves treatment adherence and symptom severity. Participants will be randomly assigned to one of two groups: one receiving active light therapy via glasses emitting cyan-colored light at 1200 Lux for 30 minutes daily upon waking for two weeks alongside CPAP, and the other receiving a sham light therapy with much lower light intensity combined with CPAP. The treatments are provided at the patient's home, with devices and monitoring equipment delivered by service providers experienced in home CPAP installation. A polysomnography test is done before treatment to confirm OSAS diagnosis. Throughout the study, researchers will track CPAP compliance at two weeks, the primary outcome measure, using data recorded by the CPAP machines. Secondary assessments include depressive symptom ratings (MADRS), sleep quality via polysomnography, actimetry monitoring, and self-reported questionnaires completed at baseline, two weeks, and four weeks. The study spans 28 days, with the first 14 days involving combined therapy and the following 14 days continuing CPAP alone. This design helps evaluate ongoing effects after stopping light therapy.

CONDITIONS

Brief 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
  • Adults diagnosed with a major depressive episode according to DSM-V with a MADRS score of 15 or higher
  • Adults diagnosed with obstructive sleep apnea syndrome (OSAS) by ventilatory polygraphy or polysomnography (AASM 2017 criteria) requiring CPAP
Not Eligible

You will not qualify if you...

  • Refusal to participate
  • Pregnant or breastfeeding women
  • Under guardianship or curatorship
  • Unstable psychiatric or physical illness (e.g., hypomania, high suicide risk) considered incompatible by investigators
  • Other psychiatric, neurologic, or somatic conditions
  • Contraindications to light therapy including retinopathy, retinitis pigmentosa, diabetic retinopathy, macular degeneration, glaucoma, or recent eye surgery within 3 months
  • Choosing a provider or device other than protocol specified
  • 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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 2 weeks

Participants receive daily light therapy using glasses (active or sham) for 30 minutes each morning combined with the introduction of CPAP treatment at home.

Daily use of light therapy glasses and CPAP at home for 14 days

Follow-up

Duration - 2 weeks

Participants continue CPAP treatment without light therapy and complete self-questionnaires and assessments to monitor sleep quality, compliance, and depression symptoms.

1 visit at Day 28 and self-questionnaires completed at Day 0, 14, and 28

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

Loading map...

Research Team

S

Sébastien S CATOIRE, Dr

L

Lydie L SARTELET, Mrs

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Similar Trials

3D Volumetric Changes in the Upper Airway After Maxillomandi...

Obstructive Sleep Apnea

Actively Recruiting

1 location

A Multicenter Retrospective Analysis of Postoperative Respir...

Obstructive Sleep Apnea

Actively Recruiting

2 locations

Sex Differences in Neurocirculatory Control With Obstructive...

Obstructive Sleep Apnea

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

Adjunctive bright light therapy to enhance continuous positive airway pressure adherence in patients with comorbid major depressive disorder and obstructive sleep apnoea syndrome: study protocol for a randomised sham-controlled trial.

Houda El Azzaoui, Sébastien Catoire, Harold Lecharpentier...

https://pubmed.ncbi.nlm.nih.gov/41401997