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Behavioral Intervention

Chatbot for Mental Health Issues

N/A
Waitlist Available
Led By Nicholas C Jacobson, PhD
Research Sponsored by Dartmouth-Hitchcock Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up each participant in the depression cohort will fill out a questionnaire to establish baseline symptoms, and they will fill out this questionnaire again after 4 and 8 weeks of using the therapy chatbot to track changes in their symptoms.
Awards & highlights
No Placebo-Only Group

Summary

This trial will test if a chatbot using artificial intelligence can effectively provide support for people with anxiety, depression, or eating issues.

Who is the study for?
This trial is for people who experience anxiety, depression, or eating disorders as confirmed by specific questionnaires (PHQ-9 for depression, GADQ-IV for anxiety, and SWED 3.0 for eating concerns). Participants will be recruited online through various platforms like Facebook and Reddit.
What is being tested?
The study is examining the effectiveness of 'Therabot', an AI chatbot designed to provide supportive behavioral interventions to individuals with mental health conditions such as anxiety, depression, or disordered eating.
What are the potential side effects?
Since this intervention involves a chatbot providing psychological support rather than medication or medical procedures, traditional physical side effects are not expected. However, users may experience emotional discomfort or distress during interactions.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~each participant in the depression cohort will fill out a questionnaire to establish baseline symptoms, and they will fill out this questionnaire again after 4 and 8 weeks of using the therapy chatbot to track changes in their symptoms.
This trial's timeline: 3 weeks for screening, Varies for treatment, and each participant in the depression cohort will fill out a questionnaire to establish baseline symptoms, and they will fill out this questionnaire again after 4 and 8 weeks of using the therapy chatbot to track changes in their symptoms. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Anxiety Symptoms
Depressive Symptoms
Eating Disorders Symptoms

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: ExperimentalExperimental Treatment1 Intervention
This group will have access to the Therabot smartphone application. They will interact with the generative chatbot daily to discuss their mental health. Each participant in this group will have some benchmark symptoms of depression, anxiety, or eating disorders. They will fill out questionnaires every 4 weeks to describe changes in symptoms.
Group II: ControlActive Control1 Intervention
This group will not have access to the Therabot App. They will fill out questionnaires every 4 weeks to describe changes in symptoms. Each participant in this group will have some benchmark symptoms of depression, anxiety, or eating disorders.

Find a Location

Who is running the clinical trial?

Dartmouth-Hitchcock Medical CenterLead Sponsor
539 Previous Clinical Trials
2,539,555 Total Patients Enrolled
24 Trials studying Depression
4,150 Patients Enrolled for Depression
Nicholas C Jacobson, PhDPrincipal InvestigatorDartmouth-Hitchcock Medical Center
2 Previous Clinical Trials
163 Total Patients Enrolled
1 Trials studying Depression
100 Patients Enrolled for Depression
~120 spots leftby Dec 2025