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Smartphone App for Cognitive Dysfunction in Anxiety Disorders

Smartphone App-based Integrated Cognitive Control Training for Cognitive Dysfunction in Anxiety Disorders: a Multi-site Randomized Control Trial - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084163
Enrollment
100
Registered
2025-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: F400- Agoraphobia Health Condition 2: F401- Social phobias Health Condition 3: F402- Specific (isolated) phobias Health Condition 4: F410- Panic disorder [episodic paroxysmal anxiety] Health Condition 5: F411- Generalized anxiety disorder

Interventions

Intervention1: Integrated Cognitive Control Training: The 8-week ICCT will comprise cognitive stimulation tasks, metacognitive strategy monitoring and generalization exercises, using a smartphone app,

Sponsors

Indian Council of Medical Research (ICMR)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Current DSM 5 diagnosis of anxiety disorders (generalized anxiety disorder, social anxiety disorder, panic disorder, or phobic anxiety disorders), Stable on medication or off medication (no changes to medication during the course of the study or in preceding 3 months) Aged 18 - 50 years, Minimum 7th std education with working knowledge in English Amenable for neurocognitive assessments and training Access to smartphone

Exclusion criteria

Exclusion criteria: History of severe mental disorders (bipolar or psychotic disorders), History of central nervous system conditions (traumatic brain injury tumours, epilepsy, stroke, degenerative disorders), Comorbid substance/behaviour addictions (alcohol and other drugs except nicotine, gambling/gaming/technology addiction) History of developmental disorders including intellectual disability Exposure to more than 3 sessions of structured psychotherapy in preceding 3 months, Exposure to brain stimulation in the preceding 3 months

Design outcomes

Primary

MeasureTime frame
Measure of anxiety severity Timepoint: Pre: Week 1, Mid: Week 4-6, Post: Week 10-12 and Follow-up: Week 20-24(if feasible)

Secondary

MeasureTime frame
Socio-occupational functioning Cognitive functions haemodynamic correlates and functional connectivity (NIMHANS site only) Intervention feasibility and acceptance metricsTimepoint: Pre: Week 1, Mid: Week 4-6, Post: Week 10-12 and Follow-up: Week 20-24(if feasible)

Countries

India

Contacts

Public ContactDr YC Janardhan Reddy

National Institute of Mental Health and Neuro Sciences (NIMHANS)

tsjaisoorya@gmail.com08026995271

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026