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Not yet recruitingNCT07364981Updated Jan 23, 2026

Gaze Contingent Attentional Reinforcement in Major Depressive Disorder

An interventional study of Aversive white noise and Music reward in Major Depressive Disorder (MDD), sponsored by Tel Aviv University. Not yet recruiting at 1 site in Israel. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-01-23.

Sponsored by Tel Aviv University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
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Study summary

The main objective of this randomized controlled trial is to evaluate whether a gaze-contingent feedback task using negative reinforcement can serve as an effective attention-modification procedure and contribute to the treatment of Major Depressive Disorder (MDD).

Read the detailed description

This randomized controlled trial uses a gaze-contingent attentional reinforcement task to modify attention allocation patterns to emotional stimuli in participants with Major Depressive Disorder. Specifically, participants will undergo 4 training sessions, during which either negative reinforcement (aversive white noise will be heard when gazing at sad faces) or positive reinforcement (music will be heard when gazing at happy faces) will be used to divert participants' gaze toward happy faces and away from sad faces. Depressive symptoms severity will be assessed before and after training (post-training and 3-month follow up) to examine changes (reduction) in symptom severity from before to after the intervention. Attention allocation will be assessed during training (i.e. online learning) as well as before and after training (i.e. transfer of learning).

02

Conditions studied

  • Major Depressive Disorder (MDD)

Keywords

  • MDD
  • attention allocation
  • positive reinforcement
  • negative reinforcement
03

In context

Depressive Disorder, Major

2,741 studies on the registry are indexed under Depressive Disorder, Major; 559 are open to participants now.

This study's planned enrollment of 60 is below the median of 80 across 2,283 interventional studies indexed under Depressive Disorder, Major.

Browse Depressive Disorder, Major studies →

Lead sponsor

Tel Aviv University is the lead sponsor of 100 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Primary diagnosis of MDD
  • MADRS>=7
  • Normal or corrected-t-normal vision

Exclusion criteria

Exclusion Criteria:

  • Present or past psychosis, manic or hypomanic episode, PTSD
  • High suicidal ideation or behavior
  • Severe alcohol or cannabis use disorder, and/or any severity of other substance use disorder (exepct nicotine use)
  • Pharmacological treatment if not stabilized for at least three months or concurrent psychotherapy
  • Current unstable or untreated medical illness
  • Current or past organic mental disorder, seizure or brain injury
  • Eye-tracking calibration difficulties
  • Post-ECT treatment
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Gaze contingent negative reinforcement

    participants will receive gaze-contingent negative reinforcement according to their viewing patterns

    Behavioral: Aversive white noise

  • Placebo comparator
    Gaze contingent positive reinforcement

    participants will receive gaze-contingent positive reinforcement according to their viewing patterns

    Behavioral: Music reward

Interventions

  • BehavioralAversive white noise

    Participants will receveve gaze-contingent negative-reinforcement feedback according to their viewing patterns, such that when gazing at the target stimuli (i.e., happy faces) the noise will stop.

  • BehavioralMusic reward

    Participants will receive gaze-contingent music-reward according to their viewing patterns, such that when gazing at the target stimuli (i.e., happy faces) the music will play.

06

What researchers measure

Primary outcomes

  1. MADRS- diagnostic interview scores

    Change from baseline- the Montgomery Asberg Depression Rating scale is a clinician-administered scale that includes 10 items that measure the severity of depressive symptoms. Each of the 10 items is scored on a 7-point scale (0-6). The total score, ranging from 0 to 60 is used to assess severity.

    Time frame: Post-treatment (1 week after treatment completion) and 3-month follow up

Secondary outcomes

  1. PHQ-9 - self report measure

    Change from baseline- the Patient Health Questionnaire-9 is a nine-question self-report questionnaire to assess the severity of depression based on symptoms over the past two weeks. Each item is scored from 0 (not at all) to 3 (nearly every day). The overal score ranges from 0-27, indicating depression severity.

    Time frame: Post-treatment (1 week after treatment completion) and 3-month follow up

Other outcomes

  1. Attention Allocation

    Changes from baseline- attention allocation towards the target stimuli (happy faces) compared to the non-target stimuli (sad faces).

    Time frame: Post-treatment (1 week after treatment completion) and 3-month follow up

  2. M.I.N.I diagnosis- diagnostic interview

    Changes in the Mini-International Neuropsychiatric Interview diagnosis. The M.I.N.I. is a structured diagnostic interview for DSM-5 and ICD-11 psychiatric disorders.

    Time frame: Post-treatment (1 week after treatment completion) and 3-month follow up

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07364981
Lead sponsor
Tel Aviv University
Responsible party
Amit Lazarov (Professor of Psychology, School of Psychological Sciences, Tel Aviv University) — Principal investigator
First posted
Jan 23, 2026
Start date
Jan 1, 2026 (estimated)
Primary completion
Jan 1, 2030 (estimated)
Completion
Jan 1, 2030 (estimated)
Last update
Jan 23, 2026

Study contacts

Shani Lavi, M.A.
Contact
shanilavi@mail.tau.ac.il
+972 50 2656664
Amit Lazarov, PhD
principal investigator · Tel Aviv University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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