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Teens in rural india to help shape mental health app

NCT ID NCT07595029

Knowledge-focused Sponsor: Wysa Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aims to adapt a digital mental health app called Wysa for adolescent girls aged 13-18 in rural Uttar Pradesh, India, who have anxiety or depression. Researchers will work with the girls, their families, and community members to identify what helps or hinders app use and co-design improvements. The goal is to create a roadmap for making the app more accessible and effective in low-resource settings.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 179 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Nov 2026

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study will be conducted in the selected Community Development Blocks (CD Blocks), an administrative subdivision of districts, across the 5 districts of Bahraich, Barabanki, Hardoi, Lucknow, and Sitapur in Uttar Pradesh.

Ages

13 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

ADOLESCENTS: Inclusion Criteria: * Sex: girls * Marital status: Unmarried * Are between 13-18 years of age * Residing in the selected villages of Uttar Pradesh, India. * Have elevated anxiety and/or depressive symptoms on the RCADS-25. * Have access to a mobile phone (at least 1 mobile phone within the family). * Provide assent/ consent to participate, along with guardian consent for minors. Adolescents Exclusion Criteria: * Adolescent girls who have difficulties that would prevent them from actively participating in workshop activities (e.g. with memory or comprehension, indications of psychoses) * Are currently or have been in the past a girl icon in the Milaan Foundation Girl Icon program PARENTS/GUARDIANS: 1. Inclusion Criteria * Are guardians or caregivers of a participating adolescent girl. * Currently reside in Uttar Pradesh * Provide informed consent to participate. 2. Exclusion Criteria ● They have difficulties that would prevent them from actively participating in workshop activities (e.g. with memory or comprehension, indications of psychoses). COMMUNITY STAKEHOLDERS \& DECISION MAKERS 1. Inclusion criteria * Contribute to and influence local health related-decisions or services. * Provide informed consent to participate. 2. Exclusion Criteria ● Stakeholders who have difficulties that would prevent them from actively participating in workshop activities (e.g. with memory or comprehension, indications of psychoses)

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder Depression depressive disorder Patient Participation

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Anxiety Anxiety disorder of adolescence Depression in adolescence

How to take part

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  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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More trials for these conditions

Other studies related to the condition(s) this trial covers.