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Creating and Testing a Tool to Measure the Harmful Effects of Excessive Screen Use on Eyes and Ears in Participants, and Comparing It with a Standard Anxiety and Depression Scale (DASS-21) in People with anxiety and depression Who has a lot of screen exposure.

Development and Validation of an Asatmyaindriyartha Samyoga(Chakshu indriya - Shravanindriya) Assessment Tool and A Cross-sectional comparitive study with DASS 21 w.s.r Screen time related Anxiety and Depression - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/12/099684
Enrollment
400
Registered
2025-12-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: F411- Generalized anxiety disorder Health Condition 2: F321- Major depressive disorder, singleepisode, moderate

Interventions

Intervention1: Nil: Nil

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Anxiety , depression diagnosed patients (based on ICD -10 criteria) Individuals with daily screen time of 6 hours or more. Individuals aged between 18- 60 Years Willing To Provide informed consent.

Exclusion criteria

Exclusion criteria: Individuals with dementia , intellectual impairment , psychotic illness Individuals With Visual or Cognitive Impairments Affecting Screen Use Patients on ongoing substance abuse. Individuals with inability to understand or complete the study questionnaire

Design outcomes

Primary

MeasureTime frame
Assessment of Extent of Asatmya Indriya Artha Samyoga among individuals with excessive screen time. Assessment of Association between AIS tool and DASS-21 scores results.Timepoint: At the end of the study (12 Months)

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactNatisha Sharma

National Institute of Ayurveda Jaipur

ssurendra452@gmail.com9414361874

Outcome results

None listed

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