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Examining the Feasibility of Wysa in Hindi

NCT06320756 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 79

Last updated 2024-12-24

No results posted yet for this study

Summary

The principal objective of this study is to investigate the feasibility of including a digital mental health intervention (Wysa in Hindi) within pre-existing usual care to support adolescents and young adults with Type 1 Diabetes (T1D) who have mild and above mental health distress (operationalized as Patient Health Questionnaire-9: 5-14 scores; or Diabetes Distress Scale-17: \>2.0 mean score) with their mental health distress. This will be conducted through an exploratory randomized control study comparing Wysa in Hindi plus usual care with a control arm that just has usual care. The study further explores the effectiveness of the digital mental health intervention using the Patient Health Questionnaire (PHQ-9) and Diabetes Distress Scale (DDS-17).

Conditions

  • Mental Health Issue
  • Diabetes Distress

Interventions

BEHAVIORAL

Wysa in Hindi

Wysa in Hindi is a blended digital mental health intervention

BEHAVIORAL

Individual and group sessions on topics like motivation, coping, wellbeing

Individual and group sessions on wellbeing, coping, and motivation with the diabetes educator team

Sponsors & Collaborators

  • Udaan

    collaborator UNKNOWN

  • Wysa

    lead INDUSTRY

Principal Investigators

  • Tejaswi Shetty, M.A. · Touchkin eServices Pvt. Ltd.

  • Archana Sarda, M.D · Udaan

  • Chaitali Sinha, M.A. · Touchkin eServices Pvt. Ltd.

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
13 Years
Max Age
25 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-23
Primary Completion
2024-05-28
Completion
2024-05-28

Countries

  • India

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06320756 on ClinicalTrials.gov