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Effects of Virtual Assistant Features on User Experience in Service Settings (AVir4Services)

18 giugno 2026 aggiornato da: Francisco Rejón-Guardia, University of Malaga

Virtual Assistants as Agents of Change: Improving User Interaction and User Experience Outcomes in Service Delivery

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.

Panoramica dello studio

Descrizione dettagliata

Virtual assistants are artificial intelligence systems that enable users to interact with digital services via text, voice, or embodied avatars. Their use does not necessarily improve user experience because interaction outcomes may depend on the design and behavior of the virtual assistant, the service context, and the characteristics of the user.

The main objective of this study is to identify the factors that influence user interaction and user experience outcomes when people engage with virtual assistants in service settings. The study will examine characteristics such as the type of virtual assistant, communication style, language specificity, anthropomorphism, personalization, adaptability, appearance, voice, level of immersion, and the occurrence of inaccurate, erroneous, or unexpected responses.

Approximately 400 adults aged 18 years or older will participate in experimental sessions conducted primarily at the Consumer Behavior Research Laboratory (LICCO) of the University of Malaga. Participants will be recruited through the Online Recruitment System for Economic Experiments (ORSEE), university communication channels, social media, collaborating organizations, and other appropriate recruitment channels.

Participants will interact with or be exposed to virtual assistants developed or configured for the study. These may include avatars, chatbots, and voice assistants presented in two-dimensional or immersive three-dimensional environments. The experimental materials may also include edited images, audio, or video representing simulated interactions with virtual assistants in tourism, cultural, retail, financial, or other service contexts.

Depending on the specific experimental design, participants will be assigned to conditions that differ in one or more virtual assistant features or interaction outcomes. The study may compare different levels of anthropomorphism, communication styles, degrees of language specificity, personalization, assistant modality, immersion, or response accuracy. The final allocation procedures and experimental conditions will be defined before recruitment and documented in the study protocol and ClinicalTrials.gov record.

After the interaction, participants will complete questionnaires assessing variables such as perceived usefulness, enjoyment, symbolic benefits, trust, satisfaction, attitude toward the recommendation, acceptance of recommendations, perceived risk, privacy concerns, emotional response, and intention to use the virtual assistant. Relevant participant characteristics, including age, gender, personality, personal innovativeness, digital experience, and accessibility needs, may also be examined as explanatory or moderating variables.

Non-invasive consumer neuroscience and psychophysiological techniques may be used during the experimental session. Eye tracking will record gaze position, visual fixations, and eye movements. Electrodermal activity will be used to assess changes in physiological arousal. Electroencephalography will record electrical brain activity associated with cognitive and emotional processing. Automated facial expression analysis will code observable facial movements and emotional expressions. Facial recordings will not be used for biometric identification, authentication, or identity verification.

Participants will receive study information and provide informed consent before data collection. A safety screening questionnaire will be administered when required for the psychophysiological procedures. Data will be coded and stored separately from directly identifying information. Results will be reported only in aggregated, anonymized, or appropriately pseudonymized form.

The study is behavioral and non-therapeutic. It does not involve medication, biological samples, medical treatment, diagnosis, or evaluation of a medical device. The procedures are non-invasive, although participants may experience temporary tiredness or minor discomfort during the experimental session.

Tipo di studio

Interventistico

Iscrizione (Stimato)

400

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Sebastián Molinillo Jiménez - Professor of Marketing, PhD
  • Numero di telefono: +34 952131265
  • Email: smolinillo@uma.es

Backup dei contatti dello studio

  • Nome: Francisco Rejón-Guardia, Associate professor of marketing, PhD
  • Numero di telefono: +34 952 13 12 68
  • Email: franrejon@uma.es

Luoghi di studio

      • Málaga, Spagna, 29013
        • Consumer Behavior Research Laboratory (LICCO), University of Malaga
        • Contatto:
          • Sebastián Molinillo Jiménez Professor of Marketing and Principal Investigator, PhD
          • Numero di telefono: +34 952 13 12 65
          • Email: smolinillo@uma.es
        • Investigatore principale:
          • Francisco Rejón-Guardia, PhD
        • Investigatore principale:
          • Sebastián Molinillo Jiménez, PhD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Scienza basilare
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: High Anthropomorphism and Accurate Response
Participants 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.
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 provide accurate, relevant, and contextually appropriate information during the simulated service interaction.
Sperimentale: High Anthropomorphism and Inaccurate Response
Participants 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.
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 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.
Sperimentale: Low Anthropomorphism and Accurate Response
Participants 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.
The virtual assistant will provide accurate, relevant, and contextually appropriate information during the simulated service interaction.
The virtual assistant will display a comparatively low level of human-like visual, vocal, or conversational characteristics, as operationalized in the experimental protocol.
Sperimentale: Low Anthropomorphism and Inaccurate Response
Participants 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.
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.
The virtual assistant will display a comparatively low level of human-like visual, vocal, or conversational characteristics, as operationalized in the experimental protocol.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Trust in the Virtual Assistant
Lasso di tempo: Immediately after the virtual assistant interaction, during the same experimental session
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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
User Satisfaction With the Virtual Assistant
Lasso di tempo: Immediately after the virtual assistant interaction, during the same experimental session
User satisfaction will be assessed immediately after the interaction using a pre-specified multi-item questionnaire. Items will be rated on a 7-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree). The satisfaction score will be calculated as the mean of the completed items. Higher scores indicate greater satisfaction.
Immediately after the virtual assistant interaction, during the same experimental session
Intention to Use the Virtual Assistant
Lasso di tempo: Immediately after the virtual assistant interaction, during the same experimental session
Participants' intention to use a similar virtual assistant in the future will be assessed using a pre-specified multi-item questionnaire. Items will be rated on a 7-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree). The overall score will be calculated as the mean of the completed items. Higher scores indicate greater intention to use the virtual assistant.
Immediately after the virtual assistant interaction, during the same experimental session
Acceptance of the Virtual Assistant Recommendation
Lasso di tempo: Immediately after the virtual assistant interaction, during the same experimental session
Acceptance of the recommendation provided by the virtual assistant will be assessed after the interaction using a 7-point response scale. Higher scores indicate greater willingness to accept or follow the recommendation.
Immediately after the virtual assistant interaction, during the same experimental session
Electrodermal Activity During the Virtual Assistant Interaction
Lasso di tempo: From the start to the end of the virtual assistant interaction, for up to 20 minutes.
Electrodermal activity will be recorded continuously during the interaction. Skin conductance responses associated with the experimental stimuli will be derived from the recorded signal and compared across experimental conditions. Greater skin conductance responses indicate greater physiological arousal.
From the start to the end of the virtual assistant interaction, for up to 20 minutes.
Visual Attention During the Virtual Assistant Interaction
Lasso di tempo: Continuously during the virtual assistant interaction, over approximately 20 minutes.
Visual attention will be measured using eye tracking. Pre-specified metrics will include fixation duration and number of fixations within defined areas of interest. The eye-tracking measures will be compared across experimental conditions.
Continuously during the virtual assistant interaction, over approximately 20 minutes.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 settembre 2026

Completamento primario (Stimato)

1 gennaio 2028

Completamento dello studio (Stimato)

1 gennaio 2028

Date di iscrizione allo studio

Primo inviato

11 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

18 giugno 2026

Primo Inserito (Effettivo)

24 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

24 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

18 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

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.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su High Anthropomorphism

3
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