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Chatbot Intervention for Anxiety and Depressive Symptoms in Young Adults

Effectiveness of a Therapy Chatbot on Anxiety and Depressive Symptoms in Subclinical Young Adults: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05762939
Enrollment
81
Registered
2023-03-10
Start date
2022-05-03
Completion date
2022-08-02
Last updated
2023-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression

Keywords

anxiety, depression, quality of life, loneliness

Brief summary

This clinical trial compares the effects of using an artificial intelligence based therapy chatbot and a self-help book to lower anxiety and depressive symptoms. The therapy chatbot (named Fido) is an application delivering support for mental health via a conversation-like interface in a highly inflected language (Polish). The team will recruit young people (aged 18-35) who currently struggle with anxiety and/or depression. The participants will use the chatbot or self-help materials for two weeks. Then, the researchers will check if using the chatbot or the book improved several aspects of mental health and the quality of life. Moreover, they will compare the groups for any differences in outcomes.

Detailed description

The primary objective of this randomized controlled trial is to evaluate the effectiveness of a chatbot-delivered cognitive-behavioural intervention on anxiety and depressive symptoms (and their correlates, such as quality of life or feelings of loneliness) in a subclinical sample of about 80 participants. The intervention results are compared to an active control intervention with popular self-help materials. Secondary objectives include the assessment and analysis of the human-chatbot therapeutic bond and general user experience. The study uses a 2 x 3 mixed factorial design with two intervention arms (Fido chatbot vs self-help book) and three time points (T1: just prior to the intervention, T2: immediately after the intervention, T3: at a follow-up one month after the previous measurement). The primary intervention lasts two weeks. All primary and secondary outcomes are assessed using self-administered online questionnaires in Polish. Each primary outcome measure is analyzed using a 2 (arms) x 2 (time points) ANOVA models with T1-T2 comparisons to test for the intervention effect and T1-T3 comparisons to check the stability of the intervention effect. Additional analyzes utilize standard NHST calculations and procedures (such as t-tests and correlation coefficients) alongside the conventional ⍺=.05 level. Similarly to the previous research in this area, no blinding is used. Participants are informed about different conditions, but the research hypotheses are masked.

Interventions

BEHAVIORALChatbot

Participants in this condition were asked to use Fido, a Polish therapy chatbot, for two weeks. No minimal requirements of usage time were enforced, but participants had to fill in five engagement check surveys during the intervention period. Each survey had to be completed in less than 24 hours.

BEHAVIORALControl (book)

Participants in this condition were told to read selected chapters from a self-help book during the two-week intervention period. No minimal requirements of usage time were enforced, but participants had to fill in five engagement check surveys during the intervention period. Each survey had to be completed in less than 24 hours.

Sponsors

Ministry of Science and Higher Education, Poland
CollaboratorOTHER_GOV
University of Social Sciences and Humanities, Warsaw
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* declaring at least mild depressive or anxiety symptoms by achieving a total score of at least 16 points on Center for Epidemiologic Studies Depression Scale Revised or at least 50 points on Penn State Worry Questionnaire * being able to visit the study site in Poznań (Poland) to complete all measurements

Exclusion criteria

* undergoing psychotherapy, coaching or psychopharmacological treatment * being diagnosed with a neurological disorder

Design outcomes

Primary

MeasureTime frameDescription
R-UCLA Score ChangeTime point 1: Just prior to the intervention. Time point 2: Immediately after two weeks of the intervention. Time point 3: One month after the previous measurement (time point 2).The total sum score of the Polish version of the Revised UCLA Loneliness Scale.
PHQ-9 Score ChangeTime point 1: Just prior to the intervention. Time point 2: Immediately after two weeks of the intervention. Time point 3: One month after the previous measurement (time point 2).The total sum score of the Polish version of the Patient Health Questionnaire-9.
PSWQ Score ChangeTime point 1: Just prior to the intervention. Time point 2: Immediately after two weeks of the intervention. Time point 3: One month after the previous measurement (time point 2).The total sum score of the Polish version of the Penn State Worry Questionnaire.
SWLS Score ChangeTime point 1: Just prior to the intervention. Time point 2: Immediately after two weeks of the intervention. Time point 3: One month after the previous measurement (time point 2).The total sum score of the Polish version of the Satisfaction With Life Scale.
PANAS Score ChangeTime point 1: Just prior to the intervention. Time point 2: Immediately after two weeks of the intervention. Time point 3: One month after the previous measurement (time point 2).The total sum scores of the Polish version of the Positive and Negative Affect Scale in two subscales (Positive and Negative Affect, separately).
STAI Score ChangeTime point 1: Just prior to the intervention. Time point 2: Immediately after two weeks of the intervention. Time point 3: One month after the previous measurement (time point 2).The total sum score of the Polish version of the State-Trait Anxiety Inventory.
CESD-R Score ChangeTime point 1: Just prior to the intervention. Time point 2: Immediately after two weeks of the intervention. Time point 3: One month after the previous measurement (time point 2).The total sum score of the Polish version of the Center for Epidemiologic Studies Depression Scale Revised.

Other

MeasureTime frameDescription
HCI ScoresTime point 2: Immediately after two weeks of the intervention.The total sum scores of six subscales from the Human-Computer Interaction Scale. Used exclusively in the chatbot arm.
LP ScoreTime point 2: Immediately after two weeks of the intervention.Individual item scores from Language Pragmaticality Scale. Used exclusively in the chatbot arm.
WAI-SR ScoreTime point 2: Immediately after two weeks of the intervention.The total sum score of the Polish version of the Working Alliance Inventory Short Revised. The Polish translation of this measure was developed by the research team. Used exclusively in the chatbot arm.
Psychoeducation Test ScoreTime point 2: Immediately after two weeks of the intervention.The total sum score of the 12-item test which assessed the participants' acquired knowledge of psychoeducation topics.
ACC ScoreTime point 2: Immediately after two weeks of the intervention.The total sum score of the Polish version of the Acceptability E-scale. Used exclusively in the chatbot arm.

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026