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Investigating Attention Patterns in Young People With Anxiety

Investigating Attention Patterns in Young People With Anxiety

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03546946
Acronym
ATTN-ANX
Enrollment
99
Registered
2018-06-06
Start date
2018-06-05
Completion date
2020-01-31
Last updated
2019-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Adolescent Behavior

Keywords

Attention, Anxiety, Adolescence

Brief summary

Adolescents with elevated anxiety have been found to direct their voluntary and involuntary attention more readily toward threatening stimuli, and spend more time dwelling upon that stimuli. Various computerised tasks have been developed to attempt to retrain these attention biases back away from threat. This study will test a newly developed intervention, that uses (eye-tracking) methods to track the gaze of the individual. This intervention is called Gaze-Contingent Music Reward Training (GC-MRT), and is designed to re-train the individual away from dwelling upon threatening stimuli (emotional faces), using their favourite music to re-infornce this learning.

Interventions

BEHAVIORALGaze-Contingent Music Reward Training

Participants will hear their selected music track playing, dependent on their gaze location, when viewing a grid on neutral and negative faces.

Participants will hear their selected music track playing, regardless of their gaze location, when viewing a grid on neutral and negative faces.

Sponsors

South London and Maudsley NHS Foundation Trust
CollaboratorOTHER
King's College London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* 12-18 years of age upon study commencement * Diagnosed generalised or social anxiety disorder (assessed by SCID) * Informed written and witnessed consent

Exclusion criteria

* Psychosis * Autism * Learning difficulties * Uncorrected abnormal vision * Current use of SSRIs

Design outcomes

Primary

MeasureTime frameDescription
Change in anxiety symtomsBaseline and post-intervention (4 weeks), and at 3-month follow up.Change in anxiety symptoms from baseline at 4-weeks on the Kiddie Schedule for Affective Disorders (KSADS), and at 3-month follow up

Secondary

MeasureTime frameDescription
Change in Self-report AnxietyBaseline and post-intervention (4 weeks), and at 3-month follow up.Change in self-report anxiety symptoms from baseline at 4-weeks on the Screen for Child Anxiety Related Disorders (SCARED), and at 3-month follow up.
Change in Dwell time on negative facesBaseline and post-intervention (4 weeks), and at 3-month follow up.Change in dwell time on negative faces, from baseline at 4-weeks, using eye-tracking measures on a free-viewing attention task, and at 3-month follow up.

Countries

United Kingdom

Contacts

Primary ContactJennifer Lau
jennifer.lau@kcl.ac.uk+44 20 7848 0678
Backup ContactStephen Lisk
stephen.lisk@kcl.ac.uk+44 20 7848 0978

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026