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Chatbot-based Internet Intervention for Stress Among University Students (Stressbot)

U

University of Social Sciences and Humanities, Warsaw

Status

Completed

Conditions

Stress, Psychological

Treatments

Behavioral: Personal resources' enhancement: self-efficacy

Study type

Interventional

Funder types

Other

Identifiers

NCT05500209
Stressbot

Details and patient eligibility

About

The aim of this study is to verify the efficacy of chatbot internet intervention for reduction of stress and improvement of quality of life among university students through the enhancement of coping self-efficacy.

Full description

University students experience high stress levels and mental health risks. Research shows that increasing resources such as coping self-efficacy can reduce stress. Internet interventions can be successfully employed to deliver programs for improving university students' mental health.

The primary objective of this randomized controlled trial is to evaluate short- and long-term efficacy of coping self-efficacy enhancing intervention in reducing university students' stress and improving quality of life. The intervention will be delivered through a Facebook Messenger chat-bot. The secondary goal is to investigate acceptability of a chat-bot delivered intervention.

Participants will be recruited via social media and randomized to 1 of 2 groups: (1) experimental condition increasing coping self-efficacy with a 7-day program delivered through a chat-bot, or (2) waitlist control group. Outcomes include perceived stress and quality of life. Measurements will be taken at baseline (T1), immediately after intervention (T2), at 1 month follow-up (T3), and at 6 months follow-up (T4). Linear mixed effects model will be used to analyze the data.

The study aims to assess Stressbot's potential benefit for improving university students' well-being. Moreover, it will provide insight into feasibility of using chat-bots for delivering smartphone-based e-health treatments.

Enrollment

372 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age of at least 18 years
  • University students
  • Mobile personal device with internet access

Exclusion criteria

  • Not meeting at least 1 inclusion criteria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

372 participants in 2 patient groups

Coping Self-Efficacy
Experimental group
Description:
Experimental condition enhancing coping self-efficacy
Treatment:
Behavioral: Personal resources' enhancement: self-efficacy
Waitlist control
No Intervention group
Description:
Waitlist control condition

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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