Feasibility and Pilot Study of a Rule-based Chatbot Application for Adolescents With Anxiety Symptoms

Haukeland University Hospital

Status: Completed

Conditions: Anxiety

Treatments: Other: Rule-based chatbot intervention with therapist-guidance

Study type: Interventional

Funder types: Other

Identifiers

NCT05758935

259293

Details and patient eligibility

About

The goal of this feasibility and pilot study is to investigate the feasibility and preliminary clinical effects of a new rule-based chatbot intervention for adolescents with anxiety symptoms. The main questions are:

• Is the intervention feasible for adolescents who are experiencing anxiety symptoms?
• How do the adolescents experience the use of the intervention?
• Does the intervention lead to a reduction in anxiety symptoms?
• Does the intervention lead to a clinically significant reliable improvement at functional level?

Full description

Anxiety is one of the most common psychiatric disorders and the anxiety symptoms typically onsets in adolescence. The anxiety symptoms may be persistent into adulthood, leading to a poorer life quality and function impairments. The goal is to prevent the development of anxiety and comorbid disorders, as well as function impairment due to anxiety symptoms. This study wishes to investigate the feasibility and preliminary clinical effects of a digital intervention in an open pre-post and 3 months follow up study. The intervention consists of a rule-based click-chatbot, combined with therapist-guidance. This study will recruit N = 30 adolescents from Norway from age 13 up to 16 years old to investigate the feasibility and preliminary clinical effects of a rule-based click chatbot-intervention, and whether it causes a reduction in anxiety symptoms and increases of life functioning. If the intervention is feasible with promising results, the study will serve as a first step to a future randomized controlled trial.

Enrollment: 25 patients

Sex: All

Ages: 13 to 16 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• reporting anxiety symptoms that hinders them in participating in daily activities
• spending time trying to avoid these anxiety symptoms
• aged 13 and up to 16 years
• can read Norwegian

Exclusion criteria

• clinical cut-off on OCD subscale on RCADS-47> 10,
• clinical cut-off on Depression subscale on RCADS-47 > 16,
• ongoing treatment
• extensive reading/writing difficulties
• extensive concentration problems

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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25 participants in 1 patient group

Mobile application

Experimental group

Description:

A six weeks, rule-based chatbot intervention

Treatment:

Other: Rule-based chatbot intervention with therapist-guidance