Ignite Creation Date:
2024-05-06 @ 8:21 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06346496
Status:
COMPLETED
Last Update Posted:
2024-04-09
First Post:
2024-03-28
Brief Title:
Young People Aged 18-25 With Depression or Anxiety Mood Participate in an LLM-based Digital Dialogue Intervention Study
Sponsor:
Institute of Psychology Chinese Academy of Sciences
Organization:
Institute of Psychology Chinese Academy of Sciences
Study Overview
Official Title:
Effect of an AI Agent Trained on a Large Language Model LLM as an Intervention for Depression and Anxiety Symptoms in Young Adults a 28-day Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2023-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study is a 28-day randomized controlled trial RCT Residents were randomly assigned to an intervention group or a waiting group according to the order in which they were successfully contacted by the staff and each user was asked to engage in a total of 28 days of dialog intervention with the Douyin companion bot and complete three psychological questionnaires on Days 1 14 and 28 however the intervention group began to receive the dialog intervention after completing the first questionnaire and the waiting group began to receive the dialog intervention after completing the third questionnaire During the first four weeks the waiting group was treated as a blank control The two groups of subjects completed the three questionnaires at exactly the same point in time Each users depression anxiety and positive and negative emotions were measured using the Patient Health Questionnaire PHQ-9 the Generalized Anxiety Disorder Scale GAD-7 and the Positive and Negative Affect Schedule PANAS respectively
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None