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Single-Session Computerized Mental Health Intervention for Rural Indian Adolescents

Evaluating the Effectiveness of a Computerized, School-Based, Single-Session Intervention for Rural Indian Adolescents

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04020549
Enrollment
0
Registered
2019-07-16
Start date
2019-07-31
Completion date
2019-08-31
Last updated
2020-06-30

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

Conditions

Anxiety, Depression, Well-Being

Brief summary

The overall aim of this project is to understand if single-session interventions are acceptable, culturally appropriate, and effective for Indian adolescents attending a rural, low-resource government school. The investigators will be examining the effects of a computerized intervention on the well-being and mental health of adolescents. The investigators hypothesize that the intervention will yield statistically significant improvements in wellbeing and mental health relative to a study skills control condition.

Interventions

BEHAVIORALGrowth, Gratitude, & Positive Activities

Reading and writing activities based on growth (designed to instill the belief that people can change), gratitude (noticing and appreciating good things in life), and behavioral activation (identifying and scheduling positive activities).

Reading and writing activities designed to teach evidence-based study strategies.

Sponsors

Sangath
CollaboratorOTHER
University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* Attending a participating secondary school * Age 12 to 18 * Literate in English

Exclusion criteria

* Unable to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Change in The Warwick-Edinburgh Mental Wellbeing ScaleBaseline, 4 week follow-up, 12 week follow-upWell-being questionnaire. Total score ranges from 14 to 70. Higher values indicate a better outcome.
Intervention Appropriateness MeasureImmediately post-intervention (i.e., 0 weeks)Questionnaire measuring the appropriateness of an intervention. Appropriateness refers to the perceived fit or relevance of an intervention. The total score ranges from 4 to 20. Higher scores indicate a better outcome.

Secondary

MeasureTime frameDescription
The EPOCH Measure of Adolescent Well-beingBaseline, 4 week follow-up, 12 week follow-upQuestionnaire with five subscales measuring engagement, perseverance, optimism, connectedness, and happiness. Each subscale score ranges from 4 to 20. Higher scores indicate a better outcome. The happiness and optimism subscales will be used as secondary outcomes for this trial. A total score is not computed.
Acceptability of Intervention MeasureImmediately post-intervention (i.e., 0 weeks)Questionnaire measuring the acceptability of an intervention. Acceptability refers to the perception that a given treatment is agreeable or satisfactory. The total score ranges from 4 to 20. Higher scores indicate a better outcome.
Patient Health Questionnaire-9Baseline, 4 week follow-up, 12 week follow-upDepression Questionnaire. The total score ranges from 0 to 27. Lower scores indicate a better outcome.
Perceived Stress Scale-4Time Frame: Baseline, 4 week follow-up, 12 week follow-upQuestionnaire measuring perceived stress. The total score ranges from 0 to 16. Lower scores indicate a better outcome.
Feasibility of Intervention MeasureImmediately post-intervention (i.e., 0 weeks)Questionnaire measuring the feasibility of an intervention. Feasibility refers to the degree to which a treatment can be successfully implemented in a given setting. The total score ranges from 4 to 20. Higher scores indicate a better outcome.
Generalized Anxiety Disorder Screener-7Baseline, 4 week follow-up, 12 week follow-upAnxiety Questionnaire. The total score ranges from 0 to 21. Lower scores indicate a better outcome. Anxiety Questionnaire. The total score ranges from 0 to 21. Lower scores indicate a better outcome. Anxiety Questionnaire. The total score ranges from 0 to 21. Lower scores indicate a better outcome. Anxiety Questionnaire. The total score ranges from 0 to 21. Lower scores indicate a better outcome. Anxiety Questionnaire. The total score ranges from 0 to 21. Lower scores indicate a better outcome.

Countries

India

Outcome results

None listed

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