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Gaze Contingent Feedback in Major Depressive Disorder (MDD)

T

Tel Aviv University

Status

Completed

Conditions

Depression, Unipolar
Depressive Disorder, Major
Depressive Disorder

Treatments

Behavioral: Attention Modification

Study type

Interventional

Funder types

Other

Identifiers

NCT02945735
TAUDEPI

Details and patient eligibility

About

The purpose of this study is to determine whether giving gaze-contingent feedback is an effective attention modification procedure, helping in the treatment of Major Depressive Disorder (MDD)

Full description

The study examines giving depressive participants gaze-contingent feedback as a novel attention training procedure. Half of the participants will receive contingent feedback while the other half would receive non-contingent "placebo" feedback.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • A signed consent form
  • Men and women between the ages of 18 and 65.
  • Meeting a current diagnosis of Major Depressive Disorder (MDD) according to the DSM-IV
  • MDD as the primary diagnosis: In cases of co-morbidity, MDD will be deemed as the most distressing and clinically significant condition among the co-morbid disorders
  • Stable pharmaco-therapy: Participants receiving a pharmacological treatment who are taking a stable medication for at least 3 months before the beginning of the procedure.

Exclusion criteria

  • Psychotic episode in the past or the present time.
  • Co-morbidity with any neurological disorder (i.e., epilepsy, brain injury).
  • Another psychotherapeutic treatment during the study.
  • Usage of neuroleptic medication.
  • Change in medication status during the study.
  • Substantial usage of drugs or alcohol in the present time.
  • Poor judgment capacity (i.e., children under 18 and special populations).
  • High Risk of Suicide.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups, including a placebo group

gaze-contingent
Experimental group
Description:
Attention modification: participants will receive gaze-contingent feedback according to their viewing patterns
Treatment:
Behavioral: Attention Modification
non-gaze contingent
Placebo Comparator group
Description:
Participants will receive non-gaze-continent feedback unrelated to their viewing patterns
Treatment:
Behavioral: Attention Modification

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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