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NCT Number: NCT06726447

Artificial Intelligence Satisfaction in Professionals and Patients

This multicenter cluster-randomized study evaluates the impact of an artificial intelligence (AI) tool on the satisfaction of healthcare professionals and patients in outpatient consultations, measuring its effect on perceived satisfaction (through a visual analog scale), the duration of consultations, and the quality and quantity of clinical data recorded. Adult patients (18-80 years) seen in outpatient centers will participate, comparing those using the AI tool with centers following the usual procedure. The tool is expected to reduce the administrative burden, improve user satisfaction and increase the efficiency and quality of the clinical registry. Recruitment will take place between December 2024 and May 2025, with final analysis planned for the end of 2025.

Recruiting

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

ACES Centers, Barcelona, Catalonia, Spain

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About this study

This multicenter cluster-randomized study aims to evaluate the impact of an artificial intelligence (AI) tool designed to optimize real-time clinical registration during outpatient consultations. Its effect on patient and healthcare professional satisfaction will be analyzed, measured using a visual analog scale (VAS) and validated tools such as the Patient Experience Questionnaire (PEQ) and the Net Promoter Score (NPS). In addition, the duration of consultations and the quantity and quality of clinical data recorded in the intervention and control groups will be compared. The intervention group will use the AI tool, while the control group will continue with the usual recording without AI. Participants will be adult patients (18-80 years) seen in health centers linked to the study, recruited by prior informed consent. AI is expected to reduce the administrative burden on professionals, allowing them to devote more time to direct care, improving both the quality of the clinical record and the patient experience. Recruitment will take place between December 2024 and May 2025, and will follow the ethical guidelines set out in the Declaration of Helsinki. This project seeks to provide evidence on the implementation of AI-based technologies in the outpatient setting and their impact on the quality of healthcare.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients between 18 and 80 years of age.
  • Patients consulting for any health reason in the outpatient clinics of the centers participating in the study.
  • Patients who sign the informed consent to participate in the study.

Exclusion criteria

  • Patients who are unable to understand or complete the questionnaires, due to:
  • Language barriers.
  • Cognitive disabilities.
  • Any other reason that prevents their adequate participation.
  • Patients who are currently participating in other clinical trials or research studies that may interfere with the results of this study.

Treatment and study plan

Artificial Intelligence Tool

Device

The intervention in this study consists of the implementation of an artificial intelligence tool for clinical registration during outpatient consultations. This technology facilitates the documentation of interactions in real time, optimizing the workflow of professionals and enabling more patient-centered care.

Primary outcomes

  1. Satisfaction with the consultation

    Time frame: From enrrolment to the end of the consultation the same day.

    measured using a 10 cm Visual Analog Scale (VAS) of satisfaction, which assesses the degree of satisfaction perceived by patients and health professionals. From no satisfaction in the left side to Completely satisfied in the right side.

Secondary outcomes

  1. Duration of the consultation

    Time frame: From enrrolment to the end of the consultation the same day.

    Total time of the consultation, measured manually from the time of entry to the time of departure of the patient.

  2. Number of clinical data recorded

    Time frame: From enrrolment to the end of the consultation the same day.

    Total number of words documented in the clinical history generated during the consultation, excluding headings

  3. Patient Experience (Patient Expectation Questionnaire - PEQ)

    Time frame: at the begining and at the end of the consultation

    Assessment of selected domains of the Patient Expectation Questionnaire (Health Service Process and Professional-Patient Communication). Format: 5-point Likert scale.

  4. Likelihood of recommendation (Net Promoter Score - NPS)

    Time frame: From enrrolment to the end of the consultation the same day.

    Patient's assessment of the likelihood of recommending the service received. Range: 0 (very unlikely) to 10 (very likely).

Other outcomes

  1. Sociodemographic variables

    Time frame: at the begining of the consultation, Just after enrrollment.

    Age (years)

  2. Sociodemographic variables

    Time frame: at the begining of the consultation, Just after enrrollment.

    Sex (Male/Female)

  3. Sociodemographic variables

    Time frame: at the begining of the consultation, Just after enrrollment.

    Nationality (Spanish/Other).

  4. Sociodemographic variables

    Time frame: at the begining of the consultation, Just after enrrollment.

    Municipality of residence (Rural/Non-rural).

  5. Sociodemographic variables

    Time frame: at the begining of the consultation, Just after enrrollment.

    Marital status (Single, Married, Divorced, Widowed).

  6. Sociodemographic variables

    Time frame: at the begining of the consultation, Just after enrrollment.

    Employment status (Active/Not active/Pensioner/Employed/Other).

  7. Sociodemographic variables

    Time frame: at the begining of the consultation, Just after enrrollment.

    Educational level (None, Primary, Secondary, Vocational training, University, Doctorate).

Study contacts

Contact information is provided by the study sponsor or research team.

Raúl Ferrer-Peña, PhD

CONTACT

[email protected]

+34607712148

Sponsors and collaborators

Lead sponsor

Universidad Autonoma de Madrid

Other

Registry information

Official study title

sAItisfACES - Impact of an Artificial Intelligence Tool on the Satisfaction of Professionals and Patients in Ambulatory Consultations: A Randomized Cluster Study

Acronym: sAItisfACES

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Dec 10, 2024
Registry last updated
Feb 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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