College campus
Chennai, Tamil Nadu, India
NCT Number: NCT06887569
This study will evaluate the effectiveness of interventions to increase engagement with mental health services among a sample of college students in Chennai, India. The study is being conducted in partnership with an arts and science college for women in Chennai. The sample will be recruited within classrooms, during college hours. All students present in the classroom per the allotted time will be introduced to the study. The research team will obtain consent from those interested after screening them for age eligibility (between the ages of 18 and 30 years). Study participants will then complete a baseline survey including questions around demographics, perceptions of their own mental health, mental health treatment history, and the PHQ-ADS, a standardized composite screening tool for depression and anxiety. The experimental design is an RCT with 4 groups, randomized at the individual level: (1) a control group, which will watch a video with information about mental health and be able to access therapy in college and at SCARF, a mental health center in Chennai, at no cost for the duration of the study; (2) a screening group, in which, in addition to the interventions in the control group, students will be informed whether their responses to the PHQ-ADS questions fit in the standard risk categories of no, mild, moderate, or severe distress and corresponding recommendations for whether to make an appointment with a counselor/therapist; (3) a rewards group, in which, in addition to the interventions in the control group, students will be provided with a cash payment for attending their first therapy session; and (4) a combined screening and rewards group. The investigators will measure interest in, and take-up of, therapy at the individual level.
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Notify Me18 year–30 year
Female
Interventional
Not applicable
Chennai, Tamil Nadu, India
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
None
Financial rewards for attending therapy
Information about screening for depression and anxiety
Time frame: Immediately after treatment (Day 1)
Student stating interest in the participant survey in booking an appointment with a study counselor, or asking to be contacted by a study counselor to discuss mental health and therapy
Time frame: From enrolment until two months after enrolment
student completing the process to make an appointment for therapy with a study counselor, through the participant survey or otherwise
Time frame: Immediately after treatment (Day 1)
This is measured in two ways: participants expressing interest in accessing a mental-healthcare app in the survey, and participants actually clicking a link to download the app.
Time frame: Immediately after treatment (Day 1)
This is measured in two ways: participants expressing interest in receiving more information about mental health, and participants actually clicking a link to access the information
Time frame: From enrolment until two months after enrolment
Data will be collected from the administrative records of the counselling office on whether participants actually attended a therapy session, as well as the number of sessions attended.
Time frame: Immediately after treatment (Day 1)
Participants are asked whether they would consider seeking therapy in future
Time frame: Immediately after treatment (Day 1)
Participants are asked what steps they would take in order to take care of their psychological well-being (for example, spending time with family, or going to a counselor)
Time frame: Immediately after treatment (Day 1)
Participants are asked to select what factors are motivating or inhibiting them in taking up therapy.
Massachusetts Institute of Technology
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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