Effects of Virtual Assistant Features on User Experience in Service Settings
AVir4Services
Virtual Assistants as Agents of Change: Improving User Interaction and User Experience Outcomes in Service Delivery
1 other identifier
interventional
400
1 country
1
Brief Summary
This study examines how the characteristics and performance of virtual assistants influence user experience in service settings. Approximately 400 adults will interact with virtual assistants presented as avatars, chatbots, or voice assistants in simulated tourism, cultural, retail, or financial service situations. Participants will be exposed to one or more experimental conditions that may differ in features such as communication style, language specificity, anthropomorphism, personalization, type of virtual assistant, level of immersion, or the presence of inaccurate responses or errors. After the interaction, participants will complete questionnaires about their perceptions, emotions, trust, satisfaction, acceptance of recommendations, and intention to use the virtual assistant. During the experimental session, non-invasive methods may be used to measure visual attention and psychophysiological responses. These methods include eye tracking, electrodermal activity, electroencephalography, and automated facial expression analysis. Facial recordings will be used to analyze emotional expressions and will not be used to identify participants. The study does not involve drugs, biological products, medical treatments, diagnostic procedures, or investigational medical devices. Its purpose is to improve scientific understanding of human interaction with artificial intelligence and virtual assistants in service environments.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 11, 2026
CompletedFirst Posted
Study publicly available on registry
June 24, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2028
Study Completion
Last participant's last visit for all outcomes
January 1, 2028
June 24, 2026
June 1, 2026
1.3 years
June 11, 2026
June 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Trust in the Virtual Assistant
Trust in the virtual assistant will be assessed immediately after the interaction using a pre-specified multi-item questionnaire. Participants will rate each item on a 7-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree). An overall trust score will be calculated as the mean of the completed items. Higher scores indicate greater trust in the virtual assistant.
Immediately after the virtual assistant interaction, during the same experimental session
Secondary Outcomes (5)
User Satisfaction With the Virtual Assistant
Immediately after the virtual assistant interaction, during the same experimental session
Intention to Use the Virtual Assistant
Immediately after the virtual assistant interaction, during the same experimental session
Acceptance of the Virtual Assistant Recommendation
Immediately after the virtual assistant interaction, during the same experimental session
Electrodermal Activity During the Virtual Assistant Interaction
From the start to the end of the virtual assistant interaction, for up to 20 minutes.
Visual Attention During the Virtual Assistant Interaction
Continuously during the virtual assistant interaction, over approximately 20 minutes.
Study Arms (4)
High Anthropomorphism and Accurate Response
EXPERIMENTALParticipants will interact with a virtual assistant displaying a high level of anthropomorphic features. The virtual assistant will provide accurate and relevant responses during the service interaction.
High Anthropomorphism and Inaccurate Response
EXPERIMENTALParticipants will interact with a virtual assistant displaying a high level of anthropomorphic features. During the service interaction, the virtual assistant will provide a predefined inaccurate or irrelevant response designed for the experiment.
Low Anthropomorphism and Accurate Response
EXPERIMENTALParticipants will interact with a virtual assistant displaying a low level of anthropomorphic features. The virtual assistant will provide accurate and relevant responses during the service interaction.
Low Anthropomorphism and Inaccurate Response
EXPERIMENTALParticipants will interact with a virtual assistant displaying a low level of anthropomorphic features. During the service interaction, the virtual assistant will provide a predefined inaccurate or irrelevant response designed for the experiment.
Interventions
The virtual assistant will display a comparatively high level of human-like visual, vocal, or conversational characteristics, as operationalized in the experimental protocol.
The virtual assistant will display a comparatively low level of human-like visual, vocal, or conversational characteristics, as operationalized in the experimental protocol.
The virtual assistant will provide accurate, relevant, and contextually appropriate information during the simulated service interaction.
The virtual assistant will provide a predefined inaccurate or contextually inappropriate response during the simulated service interaction. The error will be standardized across participants assigned to this condition and will not concern medical, safety-related, or other high-risk information.
Eligibility Criteria
You may qualify if:
- Adults aged 18 years or older.
- Able to understand the study information and provide informed consent.
- Sufficient proficiency in Spanish to understand the instructions and complete the study questionnaires.
- Able to interact with a computer-based virtual assistant and complete the experimental session.
- Willing to complete the study procedures, which may include questionnaires, eye tracking, electrodermal activity recording, electroencephalography, and facial expression recording.
You may not qualify if:
- Younger than 18 years.
- Unable to understand the study information or provide valid informed consent.
- Insufficient proficiency in Spanish to understand the instructions or complete the questionnaires.
- A visual, hearing, motor, or other condition that prevents completion of the specific experimental task and cannot be accommodated by the study procedures.
- A temporary health condition, discomfort, or technical incompatibility that, according to the study procedures, prevents safe or reliable completion of the experimental session.
- Previous participation in the same experimental protocol, when prior exposure could influence the study outcomes.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Consumer Behavior Research Laboratory (LICCO), University of Malaga
Málaga, 29013, Spain
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Francisco Rejón-Guardia, Associate professor of marketing, PhD
CONTACT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Participants will not be informed of the specific experimental hypothesis or the alternative conditions. They will be informed that the study examines user interaction with virtual assistants. Investigators conducting the experimental sessions may know the assigned condition.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate professor of Marketing and Co-Principal Investigator
Study Record Dates
First Submitted
June 11, 2026
First Posted
June 24, 2026
Study Start (Estimated)
September 1, 2026
Primary Completion (Estimated)
January 1, 2028
Study Completion (Estimated)
January 1, 2028
Last Updated
June 24, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be made publicly available because the study includes potentially sensitive questionnaire, facial recording, eye-tracking, electrodermal activity, and electroencephalography data. Aggregated and fully anonymized results may be shared in scientific publications or institutional repositories, subject to ethical, legal, and data protection requirements.