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Neuro-affective Response to Light in Depressed Adolescents and Young Adults

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University of Pittsburgh

Status

Enrolling

Conditions

Depression in Adults
Depression in Adolescence

Treatments

Other: Red Light
Other: Blue Light

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05712772
STUDY22040093
R21MH127294 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this neuroimaging pilot study is to understand developmental differences in the impact of therapeutic wavelength light (blue light) versus a non-therapeutic wavelength (red light) on emotional brain function in depression. The main questions this study aims to answer are:

  • Does acute exposure to blue light (vs red light) stabilize emotional brain function in depressed individuals?
  • Are stabilizing effects of blue light (vs red light) stronger for blue light in adolescents than young adults?

Participants will complete:

  • A magnetic resonance imaging brain scan, in which we will examine the effect of blue versus red light on emotional brain function at rest and in response to rewards and losses.
  • A pupillometry test of sensitivity to blue vs red light
  • Clinical interviews and surveys
  • Screening measures for drug and alcohol use, MRI safety, and current pregnancy [if relevant]
  • Home sleep tracking with sleep diary and actigraphy for one week

Enrollment

80 estimated patients

Sex

All

Ages

12 to 30 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elevated Depressive Symptoms [PHQ9≥5 And (Item 1≥1 or Item 2≥1)]
  • (If <18yr) Parent or guardian can attend the baseline clinical interview

Exclusion criteria

  • Unable to read and write in English
  • Intellectual disability.
  • Left or mixed handedness
  • Changes to psychotropic medication type or dosage in the past 2 months
  • Lifetime bipolar disorder or schizophrenia, or substance/alcohol disorder in the past 3 months.
  • Factors influencing light and color sensitivity (i.e., color-blindness, serious ophthalmological conditions, photo-sensitizing medication).
  • Factors influencing the ability to maintain a stable sleep schedule (i.e., shift work, severe sleep disorders, extremely late or early sleep schedule).
  • Severe medical illness, neurological disorders, or history of head trauma.
  • Current pregnancy or nursing
  • MRI contraindication (e.g., metals in the body, recent tattoo, claustrophobia)
  • Positive alcohol or substance use screen at MRI visit

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Blue then Red Light
Experimental group
Description:
Blue light (480 nm) then Red light (640 nm)
Treatment:
Other: Blue Light
Other: Red Light
Red Light then Blue Light
Experimental group
Description:
Red light (640 nm) then Blue light (480 nm)
Treatment:
Other: Blue Light
Other: Red Light

Trial contacts and locations

1

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Central trial contact

Allison Caswell, BS; Adriane M Soehner, PhD

Data sourced from clinicaltrials.gov

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